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The
HIV/AIDS eNews is published by the British Columbia Persons With AIDS
Society. This publication is a compilation of various articles
collected from numerous news sources. Opinions and information
expressed are those of the individual authors and not necessarily those
of the Society.
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City Wide Housing Coalition
Join BCPWA, City Wide Housing Coalition and a host of other concerned community groups to show your concern for accessible housing in Vancouver at the Grand March for Housing, 12pm, April 4.
Meet us at one of these starting points:
- Thornton Park at the Main Street Skytrain Station
- Hastings and Main
- Peace Flame Park at the South end of the Burrard Street Bridge
Then join us at the Vancouver Art Gallery at 1:30PM! |
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Do You Need Better Access to Information on HIV/AIDS Treatment?
Then participate in a survey!
You can help BCPWA by participating in a research project to assess the changing treatment information needs of HIV-positive people in BC. The research examines the experiences that HIV-positive people have with access to HIV/AIDS treatment information and the quality of these experiences.
To access the questionnaire, go to:
http://infopoll.net/live/surveys/s33258.htm |
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Some Changes and Updates
INCOME TAX RETURNS
February 25, 2009 through May 13th 2009. Sign up at Front Desk or call 604-893-2200. |
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POLLI & ESTHER'S CLOSET
Now by appointment only.
Members are allowed one visit per month. |
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ACTING OUT
Theatre games are now widely used as warm-up exercises for actors in Europe and North America in the following situations:
- before a rehearsal or performance
- in the development of improvisational theatre
- as a lateral means to rehearse dramatic material.
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Come and take in some drama therapy and exercises that will help with both acting skills and improvisation techniques.
Where: BCPWA Training Room
When: Tuesdays, 2-3PM, March 10 - March 31.
Sign up at BCPWA Reception or call 604-893-2200. |
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Positive Gathering


Positive Gathering is a three-day, all-inclusive event where HIV+ British Columbians come together to learn and share with their peers in a safe, open & constructive environment.
When: March 27-29th
Where: Plaza 500 Hotel (500 West 12th, Vancouver) |
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FitOne - An Introduction to Active Living
Designed for individuals seeking a more active lifestyle, FitOne aims to educate participants about the beneficial effects of exercise on HIV disease while creating a mutually supportive and motivating environment.
Intended for all fitness levels, a certified kinesiologist will assess and design programs suited for individual needs. Yoga mats and exercise equipement provided. Comfortable cloths and exercise shoes recommended. Beginners welcome.
Activities may include group walks, running clinics, and beginner's yoga. |
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Weekly sessions begin Wednesday, February 25, 2009 from 3 – 4pm in the BCPWA Training Room
For more information, please contact elginl@bcpwa.org or call 604.893-2225. Limited number of participants. Register now. |
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AmBigYouUs
Are you HIV+ and Trans? Join us at AmBigYouUs, a monthly mingling and networking event specifically for the HIV+ Trans community.
Where: BCPWA's Training Room (1st Floor)
When: First Wednesday of the month, 6-8pm
For more information, please call 604.893.2258 |
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SPIRITUAL WORKSHOP
Non-denominational, supportive, unique and fun.
Join other HIV+ men and women, lakeside at the Bethlehem Retreat Centre on Vancouver Island for a 3-night/ 4 day workshop devoted to personal spirituality. A provocative, progressive workshop created on the teachings of Mathew Fox. People come away renewed with a sense of hope, a feeling of global community and a boost to their self-esteem.
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Workshop designed and facilitated by United Church Ministers, Rev. Tim Stevenson, and spouse Rev. Gary Paterson, Minister St. Andrew's Wesley United Church. Taking time to laugh and to listen, their knowledge and kindness enhances learning and garners trust.
Organized by BCPWA Retreat Team.
Lodging and meal hosted by the Benedictine Sisters.
Transportation provided.
Spaces go quickly.
Interviews March 2-April 10, 2009.
Register for an interview 604.893.2200 or 1.800.994.2437. |
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Survey on Employment Issues for People Living with HIV/AIDS
People living with HIV are invited to participate in an online survey on HIV and employment in Canada. The purpose of this survey is to learn more about the education, training, employment and health needs of people living with HIV. Our ultimate goal is a national network that will provide employment support, information and advocacy opportunities for people living with HIV whether in or out of the workforce. Your responses to the survey will inform us on the employment-related issues that matter to you most.
The survey is available electronically and will take approximately 25 minutes to complete. You will be able to save survey responses and then submit the final version at a later date. If you would like to request a hardcopy of the survey please send your contact information to the address below.
You do not have to give personal information and we do not plan to publish personal information. If this plan changes, we will only do so with your agreement. You have the right to opt out of any question(s) at any point throughout the survey. You may choose to provide us with contact information if you would like to be kept updated on the progress of this project.
The link to the survey is provided below. The survey will be open for responses through Friday, March 13. This opportunity is unique to people with HIV. We look forward to your response to the survey.
http://www.surveymonkey.com/s.aspx?sm=BxPMtNFSCtrk5n1CZTiWPQ_3d_3d
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LifeSciences BC Announces Recipients of the 2009 LifeSciences British Columbia Awards
March 9, 2009
Vancouver - LifeSciences British Columbia today announced the recipients of the 2009
LifeSciences British Columbia Awards. They are:
Genome BC Award for Scientific Excellence:
- Dr. Ben Koop, Centre for Biomedical Research, University of Victoria
- Dr. Willie Davidson, Department of Molecular Biology and Biochemistry, Simon Fraser University
Innovation & Achievement:
- John Babcook, AMGEN British Columbia
Leadership Awards:
- Dr. Jack Saddler, Faculty of Forestry, University of British Columbia
- Dr. Julio Montaner, BC Centre for Excellence in HIV/AIDS
Medical Device Company of the Year:
- Response Biomedical Corporation
Life Sciences Companies of the Year:
- OncoGenex Pharmaceuticals
- Nexterra Energy Corporation
These awards are presented annually by LifeSciences British Columbia to
recognize individuals and organizations that have made outstanding
contributions to the development of British Columbia’s life sciences
industry across all sub-sectors, from biopharmaceuticals and medical
devices to bioproducts and bioenergy – sectors which are critical to
the economic future of the province and country.
“We all
know what a challenging business environment the world is facing,”
commented Karimah Es Sabar, President of LifeSciences British Columbia,
“So it’s even more important during such times that we celebrate and
continue to nurture these great accomplishments. These recipients have
all proven over the last year and during the course of their careers
that great science and the application and commercialization of that
science continue to be achieved right here in British Columbia. We
extend our warmest congratulations and appreciation to each of the
Award recipients.”
The awards will be presented at a gala
ceremony Wednesday, April 8th, 2009 in front of an audience of
approximately 600 biopharmaceutical, medical device, bioproducts,
bioenergy and greater life sciences community and public policy leaders
at the Hyatt Regency Hotel in Vancouver. Please visit www.lifesciencesbc.ca for full details.
The LifeSciences British Columbia Awards are presented by Ernst &
Young; Farris, Vaughan, Wills & Murphy, LLP; Genome British
Columbia; and Rx&D (Canada’s Research-Based Pharmaceutical
Companies). Media sponsor: Business in Vancouver Magazines.
About LifeSciences British Columbia:
LifeSciences British Columbia supports and represents the
biopharmaceutical, medical device, bioproducts, bioenergy and greater
life sciences community of British Columbia through leadership,
advocacy and promotion of our world-class science and industry. Via
active facilitation of partnering and investment into the life sciences
sector, British Columbia is fast becoming a global life sciences
leader. LifeSciences British Columbia is a not-for-profit,
non-government, industry-funded association.
http://www.businesswire.com
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'The law is not what I want it to be': HIV expert
HIV CRIMINALIZATION / Cross-Canada forum on HIV disclosure comes to town
March 12, 2009
KEEP PROOF OF DISCLOSURE. "The law places really onerous, heavy obligations
on people living with HIV," says forum facilitator Glenn Betteridge. He urges HIV-positive people
to document their disclosure to sex partners.
(Sarah Race photo)
“The law is not what I want it to be,” says Glenn Betteridge. “It is what it is.”
A
former lawyer and policy advisor with an extensive background in fields
related to HIV/AIDS, Betteridge was in Vancouver Mar 1 for a public
forum on the criminalization of HIV nondisclosure.
In 1998,
the Supreme Court of Canada ruled that you could be charged with
aggravated assault for failing to disclose your HIV-positive status to
a sex partner prior to having unprotected sex.
Since then, an
increasing number of HIV-positive people, including many gay men, are
being charged with, and convicted of, violent offences ranging from
aggravated sexual assault to murder.
About 25 people attended the Vancouver forum; many brought questions about the grey areas surrounding HIV disclosure laws.
The
forum was part of a Canada-wide tour hosted by the Canadian AIDS
Treatment Information Exchange (CATIE), in conjunction with the
Canadian HIV Legal network and local AIDS organizations.
“The law places really onerous, heavy obligations on people living with HIV,” says Betteridge.
Asked
how he feels about these legal obligations, Betteridge is reluctant to
comment further. He says he’d rather not express his personal views on
the subject while he’s moderating the forums, so that he can continue
to act as a more impartial facilitator.
In a recent interview
with Xtra West’s Toronto sister paper Xtra, Betteridge noted that there
are disparate viewpoints within the gay community about the best way to
handle failure to disclose allegations.
“We almost talk about
those things in a utopian aspirational way,” he said. “The idea that
people living with HIV can have unprotected sex and face no
consequences because the other parties should be looking out for
themselves, asserting that as a human right, is tenuous.”
He said he hasn’t yet made up his mind about criminalizing non-disclosure.
“I
am not sure,” he told Xtra. “It’s an issue I struggle with. I need to
have my viewpoint more informed by those people who are feeling this
profoundly to decide where I think the truth lies in this.”
For
now, Betteridge advises people who have tested positive to clearly
disclose their status to potential sex partners before the first fly is
unzipped — and to keep evidence to prove they disclosed.
For
example when meeting online for face-to-face hookups, keeping a clearly
worded email disclosure and its reply — stating that the person
understands the risks associated with sero-divergent sex — can mean
less worry about future legal fallout.
Similarly, speaking
openly and directly about one’s HIV-positive status in the company of
friends and a new date makes those friends witnesses to the disclosure,
Betteridge explains.
Vice-chair of the British Columbia Persons With AIDS Society (BCPWA) Ken Buchanan agrees that these are good ideas.
With
increasing numbers of people finding casual sex partners on websites,
he remarks, email is a practical way of keeping records of disclosure.
Consistently practicing safer sex doesn’t eliminate the need to disclose, either, Betteridge told the Vancouver forum.
When
it comes to an individual’s obligation under the law in this country,
Betteridge bluntly states, “a condom doesn’t cut it.”
Though
courts in some countries, including Canada, have made judgments based
on rates of infection for certain sexual acts, viral load, and the use
of condoms, there is to date no definitive legal ruling that practicing
safer sex belies the need for open dialogue about HIV status.
Counting
only those charges that went to trial, about 75 criminal prosecutions
for non-disclosure have taken place in Canada since 1989, the majority
of which consisted of complaints by one or more women against
HIV-positive men.
One such case, that of Charles Mzite, ended
in a BC Supreme Court conviction only hours after Betteridge’s
presentation in Vancouver. Mzite was found guilty on four counts of
aggravated sexual assault for having unprotected sex with women who
testified that they did not know he had the virus.
Betteridge says disclosure can be a factor even between HIV-positive individuals.
Although
the courts have yet to see such a case, the risks associated with
drug-resistant strains of HIV, which can be passed to someone with a
currently manageable strain, means disclosure may be required there
too.
At the core of this whole issue is the continued stigmatization of HIV, says Buchanan.
“I
know people who’ve had the disease for years, [and] people they work
with, their families don’t know. There’s very few of us that are the
public faces of HIV or AIDS.”
This stigma, and possible legal worries, he says, can discourage people from being tested regularly.
Be
open and honest with all sexual partners and get tested regularly,
Buchanan advises. Despite what may sometimes feel like a slow pace of
change, after 25 years of activism, he says, “we have to just keep at
it.”
Discuss this story here
By Patty Comeau, http://www.xtra.ca
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Keep St Paul's intact: city councillors
GAY VILLAGE / Meggs introduces motion to back hospital's renewal
March 12, 2009
WELCOME
THE MOTION. St Paul's supporters Jim Deva, Brent Granby, Jennifer
Breakspear
and Bobbie Bees were pleased with councillor Geoff Meggs'
motion to renew the West End hospital.
(Shauna Lewis photo)
The Save St Paul’s Coalition is celebrating a victory this
week after its ongoing efforts to keep the West End hospital’s programs
intact garnered unanimous support from city council’s Planning and
Environment committee.
Councillor Geoff Meggs introduced a
motion to back the hospital’s renewal and retain its key specialized
programs at the committee’s Mar 5 meeting.
“This is to put on
record our commitment to the renewal of St Paul’s as a critical
healthcare facility for the province, but also a major economic
generator for our city,” Meggs said.
The motion urges the
provincial government to consider the economic, ecological, medical and
social benefits of keeping the West End hospital’s key programs and
services intact.
The motion was unanimously supported by all
councillors present at the committee meeting: Meggs, David Cadman,
Andrea Reimer, Heather Deal, Kerry Jang and Ellen Woodsworth. Mayor
Gregor Robertson voted in favour as well.
BC health minster
George Abbott says he’s not opposed to the motion. Given its age and
structure, St Paul’s is in need of renewal and revitalization, he
acknowledges.
But whether that revitalization will occur on
the existing Burrard St site or on the proposed False Creek Flats site
is still undetermined, Abbott says.
Abbott calls the part of
the motion that refers to the provincial government’s potential
dismantling and transferring of the hospital’s key programs to other
hospitals “premature and misleading.”
“The province has made no decisions in regard to taking services away from St Paul’s,” he maintains.
However, he confirms that talks with BC’s health authorities are taking place.
“A
planning process is currently underway involving the health authorities
and the ministry regarding the utilization of acute care facilities
well into the 21st century,” Abbott reveals.
The government is
looking at how programs at Vancouver General Hospital, Surrey Memorial,
Royal Columbian and St Paul’s are best utilized, Abbott says.
Asked
if his ministry has seen any business case from St Paul’s operator
Providence health care regarding the hospital’s relocation and renewal,
Abbott says he has not.
“The spirit of the motion is something
we all would support,” says Providence spokesperson Shaf Hussain, who
says the hospital still needs major investment and renewal.
Meggs’ motion follows a Jan 30 letter sent by senior hospital staff to Premier Gordon Campbell.
“We
know there is extensive planning underway within the Ministry of Health
to develop strategic plans to address BC’s growing long-term health
care needs. We support the need for such planning,” the letter reads.
“However, any process that begins with contemplating a downgrading of
St Paul’s is inherently flawed and naive. We believe the beginning
point should be how to add to St Paul’s current levels of expertise and
human potential, not subtract from it.”
Prior to the
committee’s vote, Brent Granby, chair of the Save St Paul’s Coalition,
urged councillors to put pressure on the province to make a decision
regarding the hospital’s future. St Paul’s has been in a state of limbo
long enough, Granby told the committee.
“St Paul’s Hospital
renewal plans have been languishing for more than seven years,” he
claimed. “The lack of significant investment in capital spending in
renewing and extending the hospital has left many speculating on what
the long-term plans for the hospital are.
“The fear now is not
that it will move, but that it will be hollowed out from within,” he
said. “The province should make good on its commitment to assist on the
capital cost of this project.”
“The idea of moving discrete
programs from St Paul’s Hospital to another hospital is unrealistic,”
Dr Peter Dodek, chair of the Critical Care Working Group at the
hospital’s Centre for Health Evaluation and Outcome Sciences, told the
committee.
“Each of the key programs at St Paul’s Hospital is
intricately related to many other programs and services and the success
of these programs depends on this synergy,” Dodek said. “I believe that
we can meet these needs through incremental renewal on our existing
site, not the creation of an entirely new building on another site.”
“The
idea that you can take pieces out and move them willy nilly here or
there and still protect the health services is wrong,” Meggs agreed.
“By
passing this motion in council we make it very clear to all the
stakeholders and the province that we’re prepared to look at this
proactively, renewing St Paul’s and generating for the province the
medical benefits that will come,” Meggs said.
“Using what has
already been built and expanding on the current site is more cost
effective, more ecologically sustainable and more in line with the
historic context of the location,” Granby said.
“The economic
impact of St Paul’s is huge in the West End,” added Little Sister’s
co-owner Jim Deva. “If St Paul’s were to move, you would see For Rent
signs and For Lease signs up and down Davie and Burrard and Denman Sts.
It would be a disaster economically. If we could have a renewal of St
Paul’s hospital, I think we could have a renewal of the West End.”
Jennifer
Breakspear, executive director of The Centre on Bute St, pointed out
that the West End’s queer community, including its seniors, uses St
Paul’s services on a regular basis. “The people that need the services
are in the West End. Let’s keep the services in the West End,” she
urged.
The hospital is also vital for the many HIV-positive
people who live nearby and rely on its services, Breakspear added. “So
many of the folks living with HIV/AIDS are living in the West End. It
would be a travesty to deny those people that most need the services
access to them for various financial, economic or profiteering
motives.”
“It’s an issue that’s emotional. It’s technical.
It’s community-based. It covers all kinds of different issues,”
acknowledged councillor Heather Deal.
“It’s an urban hospital
in a very urban setting. It’s within the fabric of the neighbourhood
and the grid and transit. If every service that is there now were moved
down to the proposed site it would become a suburban hospital,” Deal
said. “It would become the kind of hospital that would be quite cleaved
off from the community it serves.”
By Shauna Lewis, http://www.xtra.ca
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HIV Co-Discoverer Goes to Court Over Rights to Potential Cure
Nobel
Prize–winning French researcher Luc Montagnier—credited as
co-discovering HIV —is being accused of stealing the intellectual
property rights to a revolutionary electromagnetic technique that may
be used to combat HIV and other diseases such as Parkinson’s and
Alzheimer’s, The Daily Telegraph reports.
March 9, 2009
Nobel Prize-winning French researcher Luc Montagnier - credited as co-discovering HIV - is being accused of stealing the intellectual property rights to a revolutionary electromagnetic technique that may be used to combat HIV and other diseases sucha s Parkinson's and Alzheimer's.
According
to the article, Montagnier is engaged in a legal battle with inventor
Bruno Robert, who approached him in May 2005 with his work on
electromagnetic waves. The following November, Robert registered a
patent for a process that would pinpoint illnesses by their
electromagnetic signature and potentially block or neutralize them with
an opposing signal. A month later, Montagnier requested a patent for
the exact biochemical process. The case went to court March 3.
Robert’s
lawyer alleges that Montagnier has already admitted that he did not
come up with the discovery, adding that the virologist had signed a
contract to use Robert’s electromagnetic technique in 2005 in exchange
for an annual payment of 100,000 euros per year over a five-year
period. Robert says he received no such payment. Montagnier’s lawyer
affirms that his client had only signed a “protocol agreement,” which
is not legally binding.
http://www.poz.com
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Center Gives L.A. AIDS Patients New Hope
Founded
by the non-profit AIDS Project Los Angeles, the new facility, located
on the campus of the former Martin Luther King Jr.-Harbor Hospital,
includes a full-service dental clinic with three operatories, a waiting
room, a one-on-one consultation room, a lab, a sterilization room, a
kitchen for food demonstrations and a food pantry.
March 6, 2009
The
doors opened this week on the S. Mark Taper Foundation Center, a
2,500-square-foot one-stop shop of vital services for persons living
with HIV/AIDS.
Founded
by the non-profit AIDS Project Los Angeles, the new facility, located
on the campus of the former Martin Luther King Jr.-Harbor Hospital,
includes a full-service dental clinic with three operatories, a waiting
room, a one-on-one consultation room, a lab, a sterilization room, a
kitchen for food demonstrations and a food pantry.
The
new center will complement the nearby OASIS Clinic HIV/AIDS Program,
which provides medical care such as hormone therapy and care
management, and the Drew Center for AIDS Research, Education and
Services (Drew CARES), an affiliate of the adjacent Charles Drew
University of Medicine and Science created to provide outreach services
to the community.
“I
always had a fear of dentists [because of] the health of my teeth,”
said Wanda, a client and 55-year-old Los Angeles Unified School
District retiree who would not disclose her full name but says she
sexually contracted the disease from her late partner, an intravenous
drug user. “Then I had a phobia because at the time people didn’t
understand HIV and AIDS so I was afraid to tell the dentist not knowing
that they know [just by] looking in your mouth,” she said. “I was
afraid that they might sue me or I might get in trouble because of the
bleeding. I didn’t know the complexity of the HIV [disease] itself. I
was still learning. So, I just started letting my teeth go because I
was scared to go to the dentist, not realizing the infection that I was
causing myself.”
As a
result she suffered from complications with eating and upset stomach
due to tooth abscesses. After a long, painful wait, her physician at
the OASIS Clinic, recommended AIDS Project L.A. Dental Services near
downtown Los Angeles.
“I
felt more cared about. They talked to me to calm my fears and walked me
through every procedure,” she added. “We talk about different things
like where I’m at with the virus and how I feel. … They make me feel
good, like somebody loves me. You know, like I’m not out here by
myself.” According to APLA, “more than 70 percent of HIV-positive
people in L.A. County need dental care, but fewer than 10 percent
receive it,” due to financial hardship, lack of transportation, and the
fear of letting their status being known.
But
APLA Executive Director Craig Thompson, who has worked for the
organization for almost 12 years, added that many who attempt to get
dental services from normal dental clinics are turned away. “In the
early days the discrimination was against the fear of HIV. Now, we have
universal precautions. …
So,
no one should be worried about that but they still are,” he said. “The
bigger issue really for most [dentists] is that HIV dentistry takes
longer because [the] HIV disease has oral manifestations and it
actually complicates normal dental procedures.”
For
a patient without HIV, he said, a typical visit or procedure can take
30 minutes. For someone with HIV, it may take 45 minutes or more. “So
dentists don’t [particularly] want to serve people with HIV because
they don’t get paid anymore and it takes twice the time. There has been
a significant economic disincentive for them to do it.”
Dr.
Steven Vitero, a medical director at APLA Dental Services who
previously owned his own private practice for 18 years, said that
during his practice “There was so much that was unknown and private
dentists didn’t want to treat patients anymore. They were afraid of the
unknown, there were even classes on how to legally get rid of
patients.”
Even today,
Vitero said, he talks to new clients who say they have been turned
away, sometimes from dentists they’ve gone to for several years.
Some
oral conditions include fungal infections, chronic gum disease,
shingles and intraoral herpes, but Kaposi’s Sarcoma — dark lesions —
remains the most frequent oral malignancy.
In
rare cases, “we will see certain lesions that are rare in the general
population with a person with a poor immune system. We’ll see warts,
we’ll see fungal infections … but they’re rarely seen, usually those
are indicators that the T-cells are down, that the immune system is not
working as well as it should be,” Vitero added.
This is why, he said, dental care is just as vital to those living with HIV/AIDS as is medical care and nutrition.
The new center’s Necessities of Life Program food pantry will coincide with the work they do at the facility.
“Proper
nutrition is a powerful tool for the successful management of HIV
disease,” said a statement from APLA. “People living with HIV often
have deficiencies in essential vitamins and minerals needed by the
immune system to fight off infection.”
Based
on a 2,000-calorie diet, every Thursday from 10:30 a.m. to 4 p.m.,
clients in the program will receive free pre-bagged groceries with
dairy products, frozen meats, whole grains, fresh fruits and
vegetables, canned and dry goods as well as personal hygiene products
and cleaning products donated by vendors. Each person can access any of
the organization’s nine food pantries a maximum of four times a month —
equivalent of up to 16 bags of groceries. The pantry is expected to
service 400 people annually.
One
of those clients will be a 65-year-old retired labor worker, who was
diagnosed with HIV in 1997. She volunteers at many of the food pantry
sites as does she make her own four monthly visits. Receiving a small
check each month for disability, she says, she wouldn’t be able to
afford medication and food without the help of the program.
“They give you good nutritional food so you stay healthy,” she said.
NOLP
program manager Tonya Hendricks said people line up at some of their
other sites three hours before opening. “For many of our clients, we
are their primary source of food,” she said. “In our program, we think
of ourselves as trying to take away the struggle of ‘Do I buy food for
my family or do I get my medications this week?’”
In
addition to an income screening, eligibility is contingent on each
person seeing a dietitian or participate in a number of nutritional
classes that focus on such things as diabetes, high blood pressure,
food-water safety and how to understand food labels.
APLA
Dental Services, established in 1985, was the nation’s first
community-based dental clinic exclusively for people with HIV/AIDS and
serves an average of 2,500 clients between its two already-established
facilities and expects to service up to an additional 500 people at its
new Watts/Willowbook facility.
Fees
and co-pays are also based on income, but “the reality is that 95
percent of the people that will use the dental clinic will be poor
enough that they have no co-pay or they will have denti-cal,” said
Thompson. Their income cannot exceed more than $1,395 per month. “The
other five percent typically have a small co-pay.”
Most
of their operating expenses will be covered by a grant from the L.A.
County Public Health Office of AIDS Programs and Policy, which also
helps fund their mobile dental clinic.
The
dental clinic at the facility will operate three days, Tuesday and
Thursday — the last day has yet to be finalized — a week from 7:30 a.m.
to 4 p.m. Vitero anticipates that the clinic will be open full time
within the next year or two once it has grown its client base.
The construction of the facility/clinic, as well as the equipment inside, costs approximately $900,000.
The
S. Mark Taper Foundation, to which it is named after, gave APLA a
$300,000 grant, the rest was gathered through public and private
partnerships — one being the M.A.C. AIDS Fund.
The
land on which it was built on was donated by the County of Los Angeles.
Thompson credits former 2nd District county Supervisor Yvonne
Braithwaite-Burke’s involvement for the facility’s completion.
Burke’s
successor, Supervisor Mark Ridley-Thomas said dental care for people
with HIV/AIDS has been identified as one of the “most-needed” services
by people living with HIV/AIDS in L.A. County.
“That’s
why I’m thrilled that this [new] AIDS Project Los Angeles [facility] is
… conveniently located near this area’s largest provider of HIV/AIDS
services, the OASIS HIV/AIDS Clinic.”
This
is the second time the S. Mark Taper Foundation provides funds to APLA.
In 2004, the foundation donated approximately $25,000 to fund an APLA
mobile clinic.
By Leiloni De Gruy, http://news.newamericamedia.org/
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Norwegian Manifesto Fights HIV Criminalization
AIDS activists in Norway seek global support to abolish stigmatizing legislation.
March 10, 2009
Norway
has become the latest country targeted in a growing global movement to
eliminate HIV criminalization laws, many of which have been attributed
to promoting stigma surrounding the virus and, therefore, discouraging
people from seeking testing and treatment.
An anonymous nonprofit Norwegian AIDS activist group called HIV
Manifesto distributed an international call-to-action on January 9. The
group was seeking signatures of support to convince the Norwegian
Parliament to abolish Section 155 of its Penal Code, which the group
believes unfairly criminalizes people living with HIV.
The section states, “Any person who has sufficient cause to believe
that he is a bearer of a generally contagious disease that is hazardous
to public health, willfully or negligently infects or exposes another
person to the risk of infection shall be liable to imprisonment for a
term not exceeding six years if the offence is committed willfully and
to imprisonment for a term not exceeding three years if the offense is
committed negligently.*”
It continues, “Any person who aids and abets such an offense shall be
liable to the same penalty. If the aggrieved person is one of the
offender’s next of kin, a public prosecution shall be instituted only
at the request of the aggrieved person unless it is required in the
public interest.”
The effects of vague, uninformed HIV criminalization are far-reaching,
and they undermine prevention and treatment efforts around the world.
In sub-Saharan Africa, more than 10 countries enforce criminal laws
concerning HIV in their alleged attempt to prevent the spread of the
virus. One such law levies criminal charges against women who don’t
take measures to prevent transmission of the virus to their offspring,
while numerous churches in Nigeria have adopted a “no test, no
marriage” law by which potential brides and grooms are required to take
HIV tests before they can wed.
Even in the United States, men and women are charged for potential HIV
exposure in circumstances where transmission is not possible. In May
2008, Willie Campbell, an HIV-positive homeless man in Dallas, was
arrested for drunk and disorderly conduct after spitting in the face of
the arresting officer. He was sentenced to 35 years in prison for
harassing a public servant because his saliva was deemed a “deadly
weapon,” despite the U.S. Centers for Disease Control and Prevention’s
(CDC) assertion that saliva has never resulted in HIV transmission.
The Norwegian manifesto is in direct response to the Justice Advisory
Group of the Norwegian Parliament’s recently proposed revision of the
Penal Code. According to HIV Manifesto, while the revision is “less
strict” and has “slightly modified” Section 155, “the criminalization
of HIV will continue.”
The group asserts this is because the Penal Code, which was introduced
in 1902 to prevent the spread of infectious diseases, as of late has
been applied only in cases specifically concerning HIV and is often
referred to as the “HIV paragraph.” Section 155 has never been
documented as a preventative measure. On the contrary, the number of
reported HIV infections in Norway has increased from 238 to 299 since
2003, when the maximum penalty was increased from three to six years.
Accordingly, Norwegian Parliament member Anette Trettebergstuen said,
“The Penal Code is not efficient as a means of reducing HIV infections.
Statistics show us clearly that the numbers of new diagnoses have
increased in recent years since the criminalization was initiated.
Information and knowledge are the right way to go, not threats of
criminal prosecutions.”
Likewise, South African Supreme Court Judge Edwin Cameron called the
manifesto an “important, well-written, informative, inspirational piece
of work.” In a recent interview with advocacy group HIV Norway, Cameron
went on to state, “Stigmatization is the driving force behind these
laws. And the laws are themselves further increasing the stigma. The
Norwegian paragraph clearly is discriminating against HIV-positive
people. It claims to regulate several diseases, but in reality it is
only being used against HIV. The government’s suggested revision will
not make any significant change or improvement.”
Consequently, HIV Manifesto believes that revising Section 155 is not
enough; instead, it wants the section completely removed from Norway’s
Penal Code to prevent any future revisions from targeting HIV-positive
Norwegians.
“To our knowledge,” stated HIV Manifesto, “this is the first time
anyone has produced a manifesto aimed at abolishing the criminalization
of HIV. We are working toward a goal bigger than removing this
paragraph: toward a reality, a future, where HIV is considered a
medical diagnosis. Period. One that comes without stigma and all the
social burdens we see in various cultures today. It was not so long ago
that cancer was considered a shame, and people withered and died at
home behind drawn curtains. Today, the stigma has vanished from that
diagnosis. In a not so distant future, we are convinced, the same will
be the case regarding HIV. We want to accelerate this process. It has
been going on too long and has caused, and still causes, immense
suffering, from gay men to housewives to African mothers.”
In light of HIV-criminalization issues such as those addressed by HIV
Manifesto, questions arise as to when punishment is in fact
appropriate. Where should a government draw the line ethically? Does it
have a fiduciary duty to punish for willing intent, or only after that
willing intent results in infection? Perhaps the Norwegian manifesto
will inspire other governing bodies to at last resolve such
persistently unsettling dilemmas.
To learn more about the manifesto, please go to hiv-manifesto-norway.blog.com.
*Translation provided by Inger-Lise Hognerud of behalf of HIV Norge.
by Nick Fowler, http://www.poz.com
|
Endothelial dysfunction in Italian cohort caused by HIV, not antiretrovirals, researchers conclude
A
retrospective cohort study has found evidence that HIV infection rather
than HIV treatment triggers a condition that is a precursor of heart
disease. The study, published in the March 13th edition of AIDS,
examined changes in markers of endothelial dysfunction, which is
characterised by damage to the smooth layer of tissue lining the blood
vessels.
March 9, 2009
A retrospective cohort study has found evidence that HIV infection
rather than HIV treatment triggers a condition that is a precursor of
heart disease. The study, published in the March 13th edition of AIDS,
examined changes in markers of endothelial dysfunction, which is
characterised by damage to the smooth layer of tissue lining the blood
vessels.
After the antiretroviral treatment breakthroughs of the late 1990s
greatly reduced HIV-related mortality in developed countries, the
cardiovascular health of HIV-positive people became a major concern.
HIV-positive people are at elevated risk of heart disease for reasons
that are not well understood. There has been much debate about whether
cardiovascular health is primarily jeopardised by certain
antiretroviral drugs or by HIV itself.
The study of endothelial markers compared three groups: HIV-positive
people initiating antiretroviral therapy, HIV-positive people who
remained treatment-naive for the full study period, and HIV-negative
controls. The two HIV-positive groups had higher levels of four markers
at baseline than the control group, an indication that they were
experiencing greater endothelial damage.
Over time, the antiretroviral therapy group had declines in three
markers while the treatment-naive group stayed the same, leading
researchers to attribute the baseline elevations in markers to HIV
rather than to antiretroviral therapy.
The study enrolled 66 HIV-positive outpatients at an Italian
clinic: 28 beginning non-nucleoside reverse transcriptase inhibitors
(NNRTIs), 28 beginning protease inhibitors (PIs), and 10 not in need of
antiretroviral therapy. The volunteers in the NNRTI group and PI group
were matched for age and sex. The control arm, comprising 28 healthy
HIV-negative volunteers, was matched for age, sex and smoking history.
The HIV-positive volunteers taking antiretroviral therapy provided
plasma samples at baseline, three months, six months, and twelve months
(all plus or minus one month). The antiretroviral-naive HIV-positive
volunteers provided samples at baseline and after twelve months. The
healthy controls provided a single round of plasma samples.
The study analysed eight markers of endothelial and platelet
activation. The markers found to be significantly higher in
HIV-positive people at baseline were soluble P-selectin (sP-sel),
soluble vascular cell adhesion molecule-1 (sVCAM-1), monocyte
chemoattractant protein-1 (MCP-1), and von Willebrand factor (VWF).
HIV-positive people taking antiretroviral therapy experienced gradual
decreases in sVCAM-1, MCP-1 and VWF levels, with these changes first
achieving statistical significance at six-month follow-up, i.e. six
months after antiretroviral therapy was initiated. In the
antiretroviral-naive group, no comparable decreases were observed.
In a subset of 20 people taking antiretroviral therapy, additional
plasma samples were obtained after 24 months. By this time, levels of
sVCAM-1 and MCP-1 (but not VWF) had decreased to the levels observed in
healthy controls.
A comparison of people who took NNRTIs and those who took PIs was
also informative. Some researchers have suspected PIs of harming the
cardiovascular system because this class of drugs is associated with
body-fat changes that are known to be risk factors for heart disease,
such as increases in cholesterol and triglyceride levels. However, the
endothelial markers for the PI group and NNRTI group did not differ
significantly during follow-up. That is, the two groups experienced
comparable declines in sVCAM-1, MCP-1, and VWF.
Interestingly, even while the PI group experienced these declines, it
also had significant increases in cholesterol and triglyceride levels.
There were no relevant baseline differences between the PI group
and the NNRTI group. Ninety-three per cent of the PI group took
lopinavir/ritonavir (Kaletra), and seven per cent nelfinavir (Viracept). Eighty-six per cent of the NNRTI group took efavirenz (Sustiva), and 14% nevirapine (Viramune).
The researchers found further evidence of the impact of HIV infection
when they compared viral load changes to sVCAM-1, MCP-1, and VWF
changes in the study participants taking antiretroviral therapy.
Decreases in viral load levels significantly correlated with the
decreases in the endothelial markers.
The study results do not rule out the possibility that long-term
use of antiretroviral therapy may harm the cardiovascular system. The
D:A:D study, a large observational cohort study, linked protease inhibitor use to a slightly elevated risk of heart attack. The D:A:D study also found that each year of exposure to PIs further increased this risk.
The researchers conclude, “A prospective study to evaluate the
long-term effects of different HAART regimens on endothelial activation
appears to be warranted, given that a late, drug-related, increase of
cardiovascular risk in the DAD study has been observed.”
Reference
Francisci D et al. HIV type 1 infection, and not short-term HAART, induces endothelial dysfunction. AIDS 23: 589 – 596, 2009.
By Kelly Safreed-Harmon, www.aidsmap.com
|
Noninvasive Hep C Test Nearly as Good as a Biopsy
Elastography—which
uses an ultrasound machine to detect the elasticity or stiffness of the
liver—has proved in some studies to be quite effective. The stiffer the
liver, the more likely it is to have damage.
March 10, 2009
A noninvasive method for determining liver damage, called transient
elastography, is nearly as accurate as a liver biopsy in people with hepatitis C virus (HCV) infection, according to a study published in the April 1 issue of Clinical Infectious Diseases.
A
liver biopsy, which involves inserting a large needle through the back
into the liver to collect tissue, can be quite painful and sometimes
results in internal bleeding and other side effects. Biopsies can also,
due to the small amount of tissue taken, underestimate the amount of
liver damage a person living with hepatitis actually has.
Because
of this, too many people infected with HCV avoid having biopsies in the
United States. Nevertheless, biopsies are the gold standard for
diagnosing liver damage in people infected with HCV and assessing the
urgency for HCV treatment.
Elastography—which uses an ultrasound
machine to detect the elasticity or stiffness of the liver—has proved
in some studies to be quite effective. The stiffer the liver, the more
likely it is to have damage. This noninvasive method has gained
increasing acceptance in Europe, but it is not yet widely available in
the United States outside research settings. Elastography has not,
therefore, been tried in significant numbers of African Americans or in
people coinfected with HCV and HIV.
To determine the method’s
accuracy in a U.S. population of people infected with HCV, Gregory
Kirk, MD, PhD, from Johns Hopkins University in Baltimore, and his
colleagues enrolled 192 HCV-infected patients participating in two
Maryland cohorts to compare elastography and biopsy results. Most of
the patients were male, African American and coinfected with HCV and
HIV.
Kirk and his colleagues found that elastography results
matched the results of liver biopsies about 85 percent of the time. In
the remaining cases where there was disparity in the results, most
people had an elastography score indicating more liver damage than was
found in the biopsy.
The authors conclude that elastography
could be useful in large clinical studies and that the technology could
one day achieve greater accuracy. In the interim, they encourage
physicians to be cautious about interpreting a single test result,
whether from elastography or biopsy, particularly when the result
indicates little to no liver damage while other tests—such as elevated
liver enzymes—suggest that liver damage is likely.
http://www.aidsmeds.com
|
Half million deaths from cryptococcal meningitis a year in people with HIV
Researchers
have estimated that there were about one million infections and a half
a million deaths from HIV-related cryptococcal meningitis worldwide in
2006. The findings published in the February 20th edition of the
journal AIDS also show that sub-Saharan Africa had the highest global
burden of cryptococcal meningitis among people living with HIV.
March 10, 2009
Researchers have estimated that there were about one million infections
and a half a million deaths from HIV-related cryptococcal meningitis
worldwide in 2006. The findings published in the February 20 th edition of the journal AIDS also show that sub-Saharan Africa had the highest global burden of cryptococcal meningitis among people living with HIV.
The scientists (led by Benjamin J. Park of the US Centers for Disease
Control) did the study because although although cryptococcal
meningitis is one of the most widely reported HIV-related opportunistic
infections, the global burden is unknown
In regions with higher HIV burdens, particularly sub-Saharan
Africa, cryptococcal meningitis has been reported to be on the increase
(more than any other type of meningitis).
Studies from Zimbabwe, Rwanda, Central African Republic, Kenya and
Tanzania have all shown increased incidence of cryptococcal meningitis
as an AIDS-defining illness and a leading cause of AIDS mortality. Away
from Africa, similar reports have emerged from India, Thailand and
Asia-Pacific (see the December 2007 edition of HATIP, a clinical review on meningitis, for more information)..
The investigators said that understanding the burden of cryptococcal
meningitis is an important public health goal that would enable
adequate planning and prioritisation of resources to enable effective
prevention of the disease.
The investigators carried out a systematic review of all available
literature published in English after 1996. Articles were selected if
they used prospective or retrospective cohort study design, reported
incidence among PLHIV or reported results which could allow calculation
of incidence among PLHIV. The researchers found 19 studies which met
eligibility criteria.
The scientists used the 2007 United Nations Programme on HIV/AIDS
(UNAIDS) estimates for adult and children prevalence as the global HIV
estimates. They used median incidence rates from available studies to
estimate region-specific cryptococcal incidence. For those regions
where data were not available, the investigators imputed the rates
using medians from regions of geographic proximity and similar economic
development level.
The researchers estimated the regional cryptococcal burdens by
multiplying the median incidence rate by the 2007 UNAIDS population
prevalence estimate for each region. They then got the sum of all
regional estimates to get the global burden of cryptococcal meningitis.
Due to variations in regional mortalities, the investigators estimated
the deaths by using case-fatality rates from clinical trials conducted
in high and middle-income countries. They also reviewed case series,
surveillance reports, reports on outcomes of cryptococcal meningitis
and consulted with clinical experts. The scientists assumed a 10-week
case fatality rate of 9% among infected people in high-income countries
and 55% for middle and low-income countries, except sub-Saharan Africa
where the estimate was 70%.
The investigators found cryptococcal incidence ranged from 4% to 12%
per year in the the reports. They had at least one eligible report per
region except for Eastern Europe and Central Asia, North Africa and the
Middle East, and the Caribbean. The incidence for Eastern Europe and
Central Asia, and North Africa and Middle East were estimated at 1.7%
per year (same as East Asia). For the Caribbean, the researchers
assumed an incidence of 3.4% per year (same as Latin America).
The scientists estimated 957,900 (range 371,700-1.54 million) cases of
cryptococcal meningitis in 2006. Sub-Saharan Africa had the highest
numbers of infection (720,000; range 144,000-1.3 million) followed by
South and South-East Asia (120,000; range 24,000-216,000). Oceania had
the fewest estimates (100 cases) followed by Western and Central Europe
(500 cases). The researchers said these estimates of both infections
and deaths will be useful for public health efforts to prevent,
diagnose and treat the disease.
The researchers further estimated about 624,725 (range 124,956-1.2
million) cryptococcal meningitis deaths in 2006. Again sub-Saharan
Africa had the highest (504,000; range 100,800-907,200) and Oceania had
the fewest (9) death estimates.
When the scientists compared the death estimates for sub-Saharan Africa
with other diseases other than HIV, they found that cryptococcal deaths
were higher than tuberculosis (350,000) which has received greater
public health attention: and were closely comparable to childhood
cluster diseases combined (530, 000), diarrhoeal diseases (708,000) and
malaria (1.1million).
The researchers acknowledged that their estimates were restricted by
limited available studies and the limitations of the available studies
themselves. They also noted that provider-based cohort studies may be
limited by incomplete follow-ups.
However, they felt the estimates are fairly accurate (particularly for
sub-Saharan Africa) because their estimates are consistent with
possible calculations from HIV cohort and natural history studies which
have reported that about 13 to 44% of AIDS deaths in the region result
from cryptococcal meningitis.
Although most of the estimates in their study were determined prior to
antiretroviral roll-out efforts, the researchers said the expansion of
treatment is not likely to impact on the global burden soon because
access to treatment is not yet universal and in some cases (such as
South Africa) the rates of cryptococcal meningitis have actually gone
up despite increased access to treatment.
Acknowledging that access to treatment can substantially reduce the
disease among PLHIV, the scientists noted that the introduction of
antiretroviral therapy has led to a drop in incidence of cryptococcal
meningitis mainly in North America and Western Europe.
The researchers said their findings emphasise the growing and future
need for attention to the problem in regions with higher HIV burden.
They suggest the expansion of accurate and simple to implement
diagnostic technologies, further research into the disease and
expansion of treatment options .
In his commentary, Thomas S. Harrison of St. George’s University,
London, acknowledged that despite study biases, there is little doubt
that HIV-related cryptococcal mortality in Africa has been
underestimated over the years..
He further said that the current study is important in stressing
the need to address the problem of cryptococcal disease. Apart from
fluconazole prophylaxis, he suggested pre-emptive fluconazole therapy
for those who screen positive for cryptococcal antigen before starting
antiretroviral treatment, suggesting that such strategy would prevent
one third of cases that present after starting antiretroviral therapy.
He concluded that many patients in Africa simply present too late for
current antifungal therapy to be effective. He also called for efforts
to facilitate earlier diagnosis and treatment and trials to compare
amphotericin B-based and oral antifungal regimens as well as to
determine the best time to start anti-HIV treatment for those diagnosed
with cryptococcal infection.
References
Harrison TS. The burden of HIV-associated cryptococcal disease (Editorial comment). AIDS, 23:531-532. 2009
Park BJ et al. Estimation of the current global burden of cryptococcal meningitis among persons living with HIV/AIDS. AIDS, 23: 525-530, 2009
By John Owuor, http://www.aidsmap.com
|
Drug resistance tests recommended for patients with suspected TB IRIS
Co-infected
HIV-TB patients with suspected TB immune reconstitution inflammatory
syndrome (IRIS) should undergo TB drug susceptibility testing before
corticosteroid treatment is considered. Furthermore, better TB IRIS
diagnostic procedures are urgently needed to differentiate TB IRIS from
other opportunistic infections.
March 10, 2009
Co-infected HIV-TB patients with suspected TB immune reconstitution
inflammatory syndrome (IRIS) should undergo TB drug susceptibility
testing before corticosteroid treatment is considered. Furthermore,
better TB IRIS diagnostic procedures are urgently needed to
differentiate TB IRIS from other opportunistic infections.
The recommendations, published in the January 23rd edition of the journal Clinical Infectious Diseases, follow a study of suspected TB IRIS patients in Cape Town, South Africa.
TB IRIS is a collection of symptoms that frequently emerge soon after
antiretroviral therapy is started in co-infected individuals. It is
believed to result from a rejuvenated immune system mounting a
TB-specific inflammatory response. Risk factors for developing TB IRIS
include low CD4 count, early initiation of anti-HIV treatment and the
existence of TB outside the lung area.
HIV-TB co-infection is a large and growing problem in sub-Saharan
Africa and, accordingly, treating TB IRIS effectively is an escalating
concern.
Suspected cases of TB IRIS are sometimes treated with
corticosteroids that are supposed to relieve symptoms by dampening the
inflammatory immune response to TB infection (inflammatory responses
are known to be a major cause of TB pathology).
A recently reported randomized study showed that a four week course of
treatment with the steroid prednisone significantly reduced the need
for medical intervention in people diagnosed with TB IRIS.
However, severe complications can arise from corticosteroid
treatment because TB IRIS diagnoses often fail to distinguish between
drug-resistant and drug-susceptible TB infections.
In patients with a previous history of TB, IRIS is a response to
lingering mycobacteria, and may lead to a paradoxical worsening of
symptoms. TB IRIS may also represent an inflammatory reaction to
previously undiagnosed TB.
In people with a drug-resistant TB infection on the other hand, IRIS is
a response to the presence of drug-resistant mycobacteria in the
tissues and the blood.
Patients undergoing TB treatment, but infected with drug-resistant TB
(or other opportunistic infections), are at risk of deteriorating
dangerously when treated with immunosuppressant corticosteroids because
first-line antibiotic treatment is pitted against resistant microbial
organisms.
In order to gain a better understanding of the extent to which TB IRIS
is misdiagnosed (or symptomatic of drug-resistant TB) the South African
research team closely scrutinised 100 suspected TB IRIS sufferers over
a 17-month period.
The patients participating in the study were in the process of
receiving TB treatment at the time that anti-HIV therapy was initiated.
Drug resistance to rifampicin was assessed with both a rapid FASTplaque-Response test and a standard (but protracted) drug-susceptibility test. TB IRIS
symptoms, as interpreted by the standard case definition, developed a
median of 14 days after anti-HIV treatment.
Seven patients suffered from an alternative opportunistic infection
that had been mistaken for TB and, more worryingly, 13 were diagnosed
with rifampicin -resistant infections. Of this subgroup, 7 were later
confirmed to have multi-drug-resistant TB.
Undiagnosed, rifampicin-resistant TB was accordingly present in 10.1%
of the study population (95% confidence interval, 3.9% to 16.4%). To
complicate matters, one patient was suspected of having developed
multi-drug resistance during the treatment programme whilst others were
suspected of being co-infected with both drug-resistant and
drug-susceptible TB.
The findings suggest that the current TB IRIS diagnostic approach
is, in many cases, inadequate. The investigators accordingly advise a
thorough investigation of alternative diagnoses before a TB IRIS
verdict is reached. Furthermore, suspected TB IRIS sufferers should
undergo extensive drug-susceptibility testing before and during
treatment to evaluate whether TB infection is (or has recently become)
resistant to treatment.
The findings support the view that corticosteroids should only be
administered to patients in whom TB drug-resistance (and
multi-drug-resistance) is absent.
The authors conclude that rapid, low-cost diagnostic procedures are
urgently needed to aid health practitioners in South Africa assess TB
drug-resistance and, hence, design better treatment regimens for
co-infected HIV-TB patients.
Reference
Meintjes, G. et al. Novel relationship between tuberculosis immune reconstitution inflammatory syndrome and antitubercular drug resistance. Clinical Infectious Diseases 48: 667-76, 2009.
By Hayden Eastwood, http://www.aidsmap.com
|
Cheaper, quieter female condom gets OK in U.S.
March 11, 2009
A
less expensive, quieter version of a female condom has gained approval
from the U.S. Food and Drug Administration, its manufacturer announced
Wednesday.
The Female Health Company said its FC2 condom is
made with a softer material that is quieter to use than the initial
version, which could make a plastic rustling sound.
The new
version is less expensive, which could make it easier to distribute to
women in Africa and other areas with high rates of HIV/AIDS.
The
approval "is an important development in efforts to deliver affordable
access to woman-initiated HIV prevention in the United States and
around the world," Female Health Co.'s strategic adviser, Mary Ann
Leeper, said in a statement.
The company's initial version was approved for use in the U.S. in 1993 to prevent pregnancy and sexually transmitted diseases.
Various brands of male condoms cost about 50 cents US, compared with between $2.80 US and $4 US for the original female condom.
Information on the cost and availability of the new version was not immediately available.
FDA approval allows the U.S. to buy FC2 for distribution to global HIV/AIDS prevention programs, Female Health said.
FC2
is also approved by the World Health Organization. The company is
seeking approval for the product in Canada, a spokesperson said.
www.cbc.ca
|
New list of HIV mutations vital to tracking AIDS epidemic
To
compile the latest list, the researchers added data from other
laboratories in Europe, Canada and the United States to include more
than 15000 sequences
March 11, 2009
In
a collaborative study with the World Health Organization and seven
other laboratories, researchers at the School of Medicine have compiled
a list of 93 common mutations of the AIDS virus associated with drug
resistance that will be used to track future resistance trends
throughout the world.
The researchers analyzed data from about
15,220 patients across the globe to develop an updated and accurate
list of the most common, resistance-related mutations of the virus. The
list was published March 6 in the online journal PLoS-One.
"The
epidemic is changing, especially as new drugs are being developed,"
said Robert Shafer, MD, associate professor of infectious diseases and
geographic medicine at Stanford and the senior author of the paper. "To
effectively track the spread of drug resistance, particularly
transmitted drug resistance, you need a sensitive and specific list
that's considered standard and is adopted by all the surveillance
studies."
The list is important, he said, as it helps
countries gauge the effectiveness of their HIV medication programs. But
assembling such a list can be a challenge, particularly with a virus
that has so many resistance-related variants.
On the one hand,
if the list is too liberally defined, then HIV drug funders and
providers may believe resistance is more widespread than is the case.
"That will cause problems in countries. They may be concerned about
whether their drugs will work," Shafer said.
On the other
hand, if the list is too restrictive, there is a risk of
underestimating the actual extent of resistance, Shafer said. "So there
is a real challenge to using the right number of mutations," he said.
In
2007, Shafer and his colleagues published a similar list of 80 HIV
mutations that has since served as the basis for global AIDS
surveillance work. However, with the scale-up of antiretroviral drug
programs in the last two years and the introduction of new medications,
resistance patterns have changed. So there was a need for a newly
updated reference, he said.
The data used in the study was
derived from a publicly available, searchable database that Shafer and
his colleagues began at Stanford in 1998. Known as the Stanford HIV RT
and Protease Sequence Database, it includes information on the two key
proteins targeted by HIV drugs: reverse transcriptase and protease.
More recently, the researchers have begun gathering resistance data on
integrase inhibitors, the latest class of antiretroviral drugs to be
introduced. However, this data was not included in the study, as these
drugs are not yet in wide use, particularly in developing countries.
To
compile the latest list, the researchers added data from other
laboratories in Europe, Canada and the United States to include more
than 15,000 sequences from untreated individuals, double the number
available in 2007. To ensure geographic diversity, information was
included for eight different subtypes of the virus, as these vary from
one region of the world to another.
The researchers scoured
the data to ensure they included only those mutations that were clearly
recognized as causing or contributing to resistance. They excluded
polymorphisms, or variants of the virus that can arise naturally, as
well as drug-related mutations that occur rarely.
The result
was that 16 new mutations were added to the 2007 list, while three were
dropped. Shafer said it was reassuring to find minimal changes were
needed.
"It shows the first list was quite good," he said.
Shafer's
Stanford colleagues in the study are Mark Kiuchi, Tommy Liu, Soo-Yon
Rhee and Jonathan Schapiro, MD. The research was funded by the National
Institutes of Health.
By Ruthann Richter, http://news.stanford.edu
|
Researchers Progress Toward AIDS Vaccine
Professors
Eddy and Gail Ferstandig Arnold Gail Ferstandig Arnold and Eddy Arnold
may have turned a corner in their search for a vaccine against HIV –
the virus responsible for AIDS. In a paper published in the Journal of
Virology, the husband and wife duo and their colleagues reported on
their research progress. With the support of the National
Institutes of Health, the Arnolds and their team have been able to take
a piece of HIV that is involved with helping the virus enter cells, put
it on the surface of a common cold virus, and then immunize animals
with it. They found that the animals made antibodies that can stop an
unusually diverse set of HIV isolates or varieties.

Photo Credit: Nick Romanenko
March 12, 2009
Professors Eddy and Gail Ferstandig Arnold Gail Ferstandig Arnold and Eddy Arnold may have turned a corner in their search for a vaccine against HIV –
the virus responsible for AIDS. In a paper published in the Journal of
Virology, the husband and wife duo and their colleagues reported on
their research progress.
With the support of the National Institutes of Health,
the Arnolds and their team have been able to take a piece of HIV that
is involved with helping the virus enter cells, put it on the surface
of a common cold virus, and then immunize animals with it. They found
that the animals made antibodies that can stop an unusually diverse set
of HIV isolates or varieties.
While researchers previously had
been able to elicit effective antibodies, they usually only acted
against a very limited number of HIV types. With HIV’s known propensity
to mutate, antibodies developed against one local strain may not
recognize and combat mutant varieties elsewhere. The challenge is to
find a broad spectrum vaccine capable of protecting against the HIV
varieties.
The Rutgers team identified a part of the AIDS
virus that is crucial to its viability – something it needs in order to
complete its life cycle – and then targeted this Achilles heel. In this
case, the part plays a role in the ability of HIV to enter cells and is
common to most HIV.
Credit: Gail Ferstandig Arnold
Human rhinovirus showing pieces of HIV (red) that stimulate helpful
immune responses displayed on the rhinovirus surface,
thereby creating a safe mimic of HIV.
The Arnolds are members of the Center for Advanced Biotechnology and Medicine, a joint research institute of Rutgers and the University of Medicine and Dentistry of New Jersey. Also, Gail Ferstandig Arnold is a research professor and Eddy Arnold is a professor, both in Rutgers’ Department of Chemistry and Chemical Biology.
While
most vaccines are actually made from the pathogen itself, employing
weakened or inactivated organisms to stimulate antibody production, HIV
is just too dangerous to use as the basis for a vaccine vehicle.
Instead, they used the relatively innocuous cold-causing rhinovirus and attached the target portion of the HIV. This must be done in a way
that maintains the HIV part’s shape so that when the immune system sees
it, it will actually mount an immune response as it would to the real
HIV.
Using recombinant engineering,
the research team developed a method to systematically test millions of
varied presentation of the HIV segment with the rhinovirus. They tried
millions of different variations on how to graft (or splice) one on to
the other, creating what are called combinatorial libraries.
“The
really exciting part is that we were able to find viruses that could
elicit antibodies against a huge variety of isolates of HIV. That is an
immense step and a very important step,” said Gail Ferstandig Arnold.
“However,
we need to be careful to not overstate things because the quantity of
response is not huge, but it is significant,” added Eddy Arnold. “This
is actually the first demonstration of this particular Achilles heel
being presented in way to generate a relevant immune response. It is
probably not potent enough by itself to be the vaccine or a vaccine,
but it is a proof of principle that what we are trying to do is a very
sound idea.”
Contact: Joseph Blumberg
732-932-7084 ext. 652
E-mail: blumberg@ur.rutgers.edu
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Ritonavir-boosted atazanavir as protease-only maintenance therapy: 48-week results
In
a small pilot study, 30 out of 34 people who had undetectable viral
loads on protease inhibitor-based triple therapy were still virally
suppressed 48 weeks after switching to a maintenance regimen of
atazanavir/ritonavir only.
March 12, 2009
In a small pilot study, 30 out of 34 people who had undetectable viral
loads on protease inhibitor-based triple therapy were still virally
suppressed 48 weeks after switching to a maintenance regimen of
atazanavir/ritonavir only. No major protease inhibitor resistance
mutations were found in any of the people whose viral load rebounded on
the simplified treatment. The findings were published in the Journal of Infectious Diseases in March.
In several studies, Kaletra (lopinavir boosted by
ritonavir) has proven surprisingly effective thus far as a maintenance
regimen – i.e., at keeping HIV viral load suppressed in people who
switch to Kaletra monotherapy after first suppressing their viral loads on a 'standard' combination regimen.
Investigators are now examining other maintenance regimens of
ritonavir-boosted protease inhibitors (PIs), such as in this
prospective, 48-week, single-arm open-label study of
atazanavir/ritonavir (Reyataz/Norvir).
This trial enrolled 36 adults who had maintained an HIV viral load
below 50 copies/ml for at least 48 weeks on their first antiretroviral
regimen – in all cases, a protease inhibitor (PI) plus two nucleoside
reverse transcriptase inhibitors (NRTIs). (In fact, most had been
suppressed for a considerable time – a median of 6.8 years.)
At study entry, all participants (except three, who were already
taking boosted atazanavir) switched from their current PI to 300mg
atazanavir plus 100mg ritonavir, once daily. Six weeks after this
switch, two had dropped out of the study (one due to a viral load
increase to 50 copies/ml); the remaining 34 then discontinued their
NRTIs.
The main end point was time to virologic failure, defined as two
consecutive HIV RNA measurements ≥ 200 copies/ml. Previously-reported
data had shown that 31 out of 34 patients (91%) maintained viral
suppression at 24 weeks after the simplification to
atazanavir/ritonavir. (This data was presented at the 13th CROI and subsequently published in JAMA).
Now, after 48 weeks, four participants failed by the stated definition:
two at 12 weeks after simplifying, one at 20 weeks and one at 28 weeks.
A fifth participant had a detectable plasma viral load of 508 copies/ml
at the last study visit, unconfirmed by a second measurement.
Counting only the four repeated failures, the probability of
virologic success at week 48 was 88%, with a lower one-sided 90%
confidence interval [CI] limit of 81%. Counting the fifth participant
as a treatment failure, the success rate was 84% (lower 90% CI, 76%).
Finally, using a stricter definition of failure (repeated – although
not single – HIV RNA measurements of ≥ 50 copies/ml), the success rate
was 82% (lower 90% CI, 73%). (None of these figures include the single
participant who withdrew due to viral rebound after switching to
atazanavir, but before dropping the NRTIs.)
The study also examined blood plasma levels of atazanavir, residual
(low-level) viraemia, and drug resistance mutations. No major
PI-associated resistance mutations were found by standard population
genotyping in any of the five participants with virologic rebound,
although several "minor" mutations (I64V and G73S) were identified. In
eight virally suppressed participants who received single-copy assay
(SCA) viral load testing, there were no significant differences in HIV
RNA levels throughout the course of the study; median levels were less
than 1.1 copies/ml overall at 48 weeks.
Atazanavir blood plasma concentrations were measured monthly, and
were linked to likelihood of treatment failure. Three participants had
undetectable atazanavir concentrations at least once during the study.
Two of these three (67%) went on to virologic failure, which occurred
in only in two of the 31 (6%) who had consistently detectable
atazanavir levels, "strongly suggest[ing] that suboptimal adherence was
an important factor in the development of virologic failure." Median
plasma concentrations of atazanavir were also lower, although not
statistically significantly, in participants with virologic failure
(380 ng/ml vs 660 ng/ml, p=.18).
While noting that this was a non-randomised pilot study of patients
with a very stable treatment history, the researchers concluded that it
"adds to a growing body of data that simplified maintenance therapy
with a boosted PI alone is effective in maintaining virologic control
after initial suppression with a 3-drug regimen." Adherence and
adequate drug concentrations may be particularly important in the
continued success of such simplified treatments.
Reference
Wilkin TJ et al. Regimen simplification to atazanavir-ritonavir
alone as maintenance antiretroviral therapy: final 48-week clinical and
virologic outcomes. JID 199: 866-871, 2009.
By Derek Thaczuk, http://www.aidsmap.com
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Efavirenz dose reduction safe for patients with gene associated with high drug levels and side-effects
Doses
of efavirenz (Sustiva) can be safely reduced by up to two-thirds in
patients who develop side-effects if these are due to a genetic
mutation resulting in high concentrations of the drug, Japanese
investigators report.
March 12, 2009
Doses of efavirenz (Sustiva)
can be safely reduced by up to two-thirds in patients who develop
side-effects if these are due to a genetic mutation resulting in high
concentrations of the drug, Japanese investigators report in the
January 28th edition of AIDS. Furthermore, a Japanese company has developed a low-cost test to see which patients have this mutation.
Efavirenz is metabolised by the liver using the p450 2B6 (CYP2B6)
pathway. Earlier research has shown that patients who have a mutation,
or polymorphism, in the gene associated with metabolising efavirenz
called CYP2B6 516G>T have extremely high blood levels of the drug
when treated with the drug’s standard once-daily dose of 600mg.
Japanese investigators performed a study to see if was possible to
reduce the dose of efavirenz in patients with this polymorphism who had
high concentrations of efavirenz.
Their study involved twelve individuals. Five had their dose of
efavirenz reduced to 400mg once daily, the other seven to 200mg daily.
Viral load remained undetectable in all twelve individuals.
Nine of the patients had experienced chronic central nervous system
side-effects when taking full-dose efavirenz. However, these
side-effects improved in nine individuals on reduction of the efavirenz
dose.
They highlight the case of a 71-year-old man who had reported virtually
nightly nightmares after starting full-dose efavirenz treatment. His
blood concentrations of the drug were extremely high and tests revealed
that he had the genetic mutation associated with high levels of the
drug.
Reduction of his efavirenz dose to 400mg daily resulted in a dramatic
improvement in his dreams. His efavirenz concentrations nevertheless
remained high and further reduction of the daily dose to 200mg resulted
in a complete disappearance of his dreams. Levels of the drug in his
blood were within target levels and his viral load was still
undetectable two years after the dose of the drug was reduced to 200mg.
Cost had been highlighted as a potential barrier to testing
efavirenz-treated patients for the mutation associated with high
concentrations of the drug. However, the investigators report that a
Japanese company has developed a test costing approximately US$75,
“thus, the financial benefits of reducing efavirenz dosage should
compensate for the cost of genotyping”, they suggest. However they note
“further larger-scale studies are needed to discuss genotype-based
tailored efavirenz treatment.”
Reference
Gatanaga, H. et al. Successful genotype-tailored treatment with small-dose efavirenz. AIDS 23: 433, 2009.
By Michael Carter, http://www.aidsmap.com
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