>TRACKING DRUG RESISTANCE IN SOUTH AFRICA
>Andrew McIntyre on Thabo Mbekis determination to buck conventional wisdom
>on AIDS
>
>By Andrew McIntyre
Wow. This is a real piece of yellow journalistic bullshit!!!
Phew....let's begin.
>The Australian Financial Review 31 March 2000
>
[quoted text clipped - 4 lines]
>literature alleging, among other things, the toxicity of this drug is such
>that it is in fact a danger to health".
OK--so this was written nearly 5 years ago. Recently, unfortunately,
he reiterated his resistance to access to ARV for pregnant women.
http://news.bbc.co.uk/1/hi/world/africa/1808986.stm
But he clearly seems to think HIV exists and causes AIDS at this
point. He isn't that stupid.
>While the news was briefly reported in Australia and elsewhere, the extent
>of the reaction and the furious debate that has followed in South Africa,
[quoted text clipped - 3 lines]
>Britain and South Africa and asked for an official inquiry into the issue
>by the Minister for Health, Dr Manto Tshabalala-Msimang.
Yeah. Boy, is she ever a piece of work.
>His announcement produced bafflement and intense anger amongst health
>professionals who maintain that AZT is safe and believe Mbeki has
>political motives. The drugs manufacturer, Glaxo-Wellcome, responded that
>it was unaware of any such lawsuits. AZT is the mainstay of international
>efforts to treat AIDS patients and to prevent the transfer of the virus
>from HIV positive mothers to their babies.
Ah, this was inaccurate even then. AZT monotherapy is used for
preventing mother-to-child transmission. Or a single dose of
nevirapine. It works pretty well for that (AZT) but may result in the
mother developing resistance.
>Dr Joseph Perriens, the head of the care and support division of the UN
>AIDS program in Geneva, suggested Mbeki "inform himself better... [and]
[quoted text clipped - 10 lines]
>Papadoupoulos, which claims its work shows that AZT is, pharmacologically,
>a failure.
LOL. If Mbeki DID buy the ravings of Papadoupoulos, he is a bigger
idiot than I thought. She's never actually done any research!! Just a
lot of armchair theorizing.
However, there IS a big issue with regard to costs of the drugs, and
the pharma held notion that intellectual property rights trump human
life.
>The drug manufacturers and clinical AIDS specialists claim that the drug
>improves "quality of life" and can reduce transmission of HIV. But Mbekis
[quoted text clipped - 3 lines]
>clear scientific proof that AZT kills HIV or cures AIDS, but that there is
>ample evidence that it kills humans.
Wow. Dead cold lies here.
>As evidence, they cite the 1994 publication of results from the Concorde
>trial, the most thorough double-blind randomised comparison of two
[quoted text clipped - 12 lines]
>Concorde study as flawed and said that its findings would not affect
>medical practice.
Concorde studied AZT monotherapy and discovered it doesn't do much for
people as a monotherapy. No one disputes that.
However, combinations of antiretrovirals have since proven that the
drugs do work to slow disease progression and vastly reduce mortality.
So this is disingenuous in the extreme.
>However, there are some eminent professionals ringing alarm bells. Dr
>Donald Abrams, professor of medicine and director of the AIDS program at
[quoted text clipped - 4 lines]
>survivors of AIDS was their resolve not to take AZT and other
>anti-retrovirals.
This is probably a very old quote. A lot of people wait to do ARV and
now the data show that waiting until the CD4 count falls between
200-300 is probably the best time to start. Early intervention is not
really all that useful.
>An article in last years June New Scientist reported that French doctors
>had linked a rare but fatal childhood neurodegenerative illness to
>exposure to AZT while still in the womb and during or shortly after birth.
What data?
>Dutch AIDS specialist Kees Brinkman, of Amsterdams Onze Lieve Vrouwe
>hospital, claims that several other side-effects may be explained by the
[quoted text clipped - 6 lines]
>cells. Brinkman concluded, "I strongly believe that [these anti-viral
>drugs] are much more toxic than we considered previously."
The drugs ARE toxic. No question. AIDS is MORE toxic. It's about risk,
benefit and limitations.
>An Italian study published last May in the journal AIDS claimed that
>HIV-positive mothers who took AZT had children with "a higher probability
[quoted text clipped - 3 lines]
>obscure-sounding condition of "mitochondria dysfunction", two of whom
>died.
It's not so obscure any more. This is why the use of nutritional
supplements to minimize mitochondrial damage make sense and require
further clinical evaluation.
>Building on this evidence, AZT critics say that the very symptoms of AIDS
>we have become familiar with, particularly severe wasting, may not be
[quoted text clipped - 6 lines]
>start. In fact, the main targets for the makers of these drugs are those
>without symptoms.
This is also a distorition of current clinical practice in places
where ARV is available. He acts like AZT is the only HIV medicine.
Idiot.
>Dr Stephen Kent, senior research fellow at the AIDS pathogenesis research
>unit of the Macfarlane Burnet Centre for Medical Research in Melbourne,
[quoted text clipped - 4 lines]
>vulnerable people who are struggling with life-saving but
>difficult-to-manage HIV treatments".
Dr. Kent is correct.
>Sceptical scientists claim the contrary that there is still no study
>proving that any of these cocktails, separately or together, can extend
[quoted text clipped - 4 lines]
>friend of Mbekis, the President said, "What do you do if professors wont
>read articles about subjects they write about?"
Nonsense....see:
>Dr Kent has described the debate questioning existing treatments and
>research as "irrelevant" and "a disgraceful waste of time and resources".
[quoted text clipped - 4 lines]
>registered." To which the South Africas health minister replied "If it is
>the first time, then somebody has to start"
The fact that AIDS is killing so many young adults in Africa should
give them a clue.
>With billions of dollars in drug-company profits and research grants at
>stake, not to mention reputations, Mbeki is under enormous domestic and
[quoted text clipped - 5 lines]
>for it), it is surprising that the Western media is not taking more of an
>interest in these difficult questions.
Mbeki should be under pressure. His policies are as sick and insane as
the pharmaceutical industry's blocking of generic antiretrovirals.
>Andrew McIntyre is a Melbourne writer who has written on HIV and AIDS for
>several years.
Well, he should retire. He's about as dumb as Gina Kolata. Maybe
dumber, if that's conceivable.
Abstracts relevant to my comments below.
George M. Carter
**
Vermund SH. Prevention of Mother-to-Child Transmission of HIV in
Africa.Top HIV Med. 2004 Dec-2005 Jan;12(5):130-4.
The University of Alabama at Birmingham, Birmingham, AL, USA.
HIV infection and mortality rates in African children are
astoundingly high. Risk factors for mother-to-child transmission of
HIV include maternal plasma viral load and breastfeeding. With regard
to the latter, current data indicate that mixed feeding (breastfeeding
with other oral foods and liquids) is associated with the greatest
risk of transmission. Studies are under way to determine if exclusive
breastfeeding with rapid early weaning can reduce transmission rates
in the absence of exclusive formula feeding for all infants. Perinatal
transmission rates have been dramatically reduced with the use of
single-dose nevirapine, but this strategy protects only approximately
50% of infants, and more than 75% of women receiving nevirapine
develop a major nevirapine resistance mutation. In developed areas of
the world, antiretroviral therapy has reduced perinatal transmission
by more than 90% compared with 1993 rates. Improved HIV-related care
for HIV-infected women in Africa is needed to reduce rates of HIV
infection in children and to prevent maternal mortality. This article
summarizes a presentation by Sten H. Vermund, MD, PhD, at the
International AIDS Society-USA course in Chicago in May 2004.
**
Imamichi T. Action of anti-HIV drugs and resistance: reverse
transcriptase inhibitors and protease inhibitors. Curr Pharm Des.
2004;10(32):4039-53.
Applied and Development Research Program, National Institute of
Allergy and Infectious Diseases at Frederick, Science Applications
International Corporation-Frederick, Inc., Frederick, MD 21702, USA.
timamichi@niaid.nih.gov
Currently, 20 drugs have been approved for Human Immunodeficiency
Virus type-1 (HIV-1) clinical therapy. These drugs inhibit HIV-1
reverse transcriptase, protease, or virus entry. Introduction of a
combination therapy with reverse transcriptase inhibitors and protease
inhibitors has resulted in a drastic decrease in HIV-1 related
mortality. Although the combination therapy can suppress viral
replication below detection levels in current available assays, low
levels of on-going viral replication still persist in some patients.
Long-term administration of the combination therapy may increase
selective pressure against viruses, and subsequently induce emergence
of multiple drug-resistant HIV-1 variants. Attempts have been made to
design novel antiretroviral drugs that would be able to suppress
replication of the resistant variants. At present, several
investigational drugs are being tested in clinical trials. These drugs
target not only the resistant variants, but also improvement in oral
bioavilability or other viral proteins such as HIV-1 integrase,
ribonuclease H, and HIV-1 entry (CD4 attachment inhibitors, chemokine
receptors antagonists, and fusion inhibitors). Understanding
mechanism(s) of action of the drugs and mechanisms of drug resistance
is necessary for successful designs in the next generation of
anti-HIV-1 drugs. In this review, the mechanisms of action of reverse
transcriptase- and protease-inhibitors, and the mechanism of
resistance to these inhibitors, are described.
**
Pereira CF, Paridaen JT. Anti-HIV drug development--an overview. Curr
Pharm Des. 2004;10(32):4005-37.
Eijkman-Winkler Center, Hp G04.614, University Medical Center
Utrecht, Heidelberglaan 100, 3584 CX Utrecht, The Netherlands.
c.f.pereira@lab.azu.nl
Highly active antiretroviral therapy (HAART) has markedly
decreased mortality and morbidity in the developed world. HAART
consists of a combination of three or more of the following classes of
antiretroviral (ARV) drug: reverse transcriptase inhibitors, protease
inhibitors and a recently approved fusion inhibitor. However, HAART
cannot completely eradicate HIV from the body, results in long-term
toxicity and eventually leads to the emergence of drug-resistant HIV
strains. These problems prompt the search for potent new drugs that
are active against drug-resistant viral strains and that can safely be
combined with other ARV drugs. The aim of this review was to give an
overview of new compounds in preclinical or early clinical development
that interact with various steps in the HIV life cycle: virus-cell
attachment; gp120-CD4 binding; gp120-coreceptor binding; viral fusion;
viral assembly and disassembly; reverse transcription; nuclear import
of the pre-integration complex; proviral integration; viral
transcription; processing of viral transcripts and nuclear export;
assembly of new virions; cellular factors involved in HIV replication.
There's lots more...
PaulKing - 20 Feb 2005 02:32 GMT
"She's never actually done any research!!"
What a stupid lie.
"ceptical scientists claim the contrary — that there is still no study
>proving that any of these cocktails, separately or together, can extend
>life. In South Africa, material critical of AZT has become central to the
>debate,"
Not nonsense. FACT
GMCarter - 20 Feb 2005 10:50 GMT
>"She's never actually done any research!!"
>
>What a stupid lie.
Not in the lab she hasn't.
PaulKing - 21 Feb 2005 02:53 GMT