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HINDUSTAN TIMES
July 16, 2008 Wednesday 2:02 PM EST
Indian-origin scientist claims to uncovering Achilles Heel of HIV
BYLINE: Report from Asian News International brought to you by HT Syndication.
LENGTH: 809 words
DATELINE: WashingtonWashington, July 16 — An Indian-origin researcher studying Human Immunodeficiency Virus (HIV) at The University of Texas Medical School at Houston claims that his team has uncovered the Achilles heel in the armour of the HIV virus.
Sudhir Paul, Ph.D., has found that this weak spot is hidden in the HIV envelope protein gp120. This protein is essential for HIV attachment to host cells, which initiate infection and eventually lead to Acquired Immunodeficiency Syndrome or AIDS.
Normally the body?(EURO)(TM)s immune defences can ward off viruses by making proteins called antibodies that bind the virus, but no HIV preventative vaccine that stimulates production of protective antibodies is available.
The Achilles heel, a tiny stretch of amino acids numbered 421-433 on gp120, is now under study as a target for therapeutic intervention.
?(EURO)oeUnlike the changeable regions of its envelope, HIV needs at least one region that must remain constant to attach to cells. If this region changes, HIV cannot infect cells. Equally important, HIV does not want this constant region to provoke the body?(EURO)(TM)s defense system. So, HIV uses the same constant cellular attachment site to silence B lymphocytes – the antibody producing cells. The result is that the body is fooled into making abundant antibodies to the changeable regions of HIV but not to its cellular attachment site. Immunologists call such regions superantigens. HIV?(EURO)(TM)s cleverness is unmatched. No other virus uses this trick to evade the body?(EURO)(TM)s defenses,?(EURO) said Paul.
Paul is the senior author on a paper about this theory in a June issue of the journal Autoimmunity Reviews. Additional data supporting the theory are to be presented at the XVII International AIDS Conference Aug. 3-8 in Mexico City in two studies titled ?(EURO)oeSurvivors of HIV infection produce potent, broadly neutralizing IgAs directed to the superantigenic region of the gp120 CD4 binding site?(EURO) and ?(EURO)oeProspective clinical utility and evolutionary implication of broadly neutralizing antibody fragments to HIV gp120 superantigenic epitope.?(EURO)
Paul?(EURO)(TM)s group has engineered antibodies with enzymatic activity, also known as abzymes, which can attack the Achilles heel of the virus in a precise way.
?(EURO)oeThe abzymes recognize essentially all of the diverse HIV forms found across the world. This solves the problem of HIV changeability. The next step is to confirm our theory in human clinical trials,” Paul said.
He stressed that abzymes degrade the virus permanently unlike regular antibodies. A single abzyme molecule inactivates thousands of virus particles. Regular antibodies inactivate only one virus particle, and their anti-viral HIV effect is weaker.
Usually, the abzymes are derived from HIV negative people with the autoimmune disease lupus and a small number of HIV positive people who do not require treatment and do not get AIDS.
?(EURO)oeWe discovered that disturbed immunological events in lupus patients can generate abzymes to the Achilles heel of HIV. The human genome has accumulated over millions of years of evolution a lot of viral fragments called endogenous retroviral sequences. These endogenous retroviral sequences are overproduced in people with lupus, and an immune response to such a sequence that resembles the Achilles heel can explain the production of abzymes in lupus. A small minority of HIV positive people also start producing the abzymes after decades of the infection. The immune system in some people can cope with HIV after all,?(EURO) said Stephanie Planque, lead author and UT Medical School at Houston graduate student.
Carl Hanson, Ph.D., who heads the Retrovirus Diagnostic Section of the Viral and Rickettsial Disease Laboratory of the California Department of Public Health, has shown that the abzymes neutralize infection of human blood cells by diverse strains of HIV from various parts of the world. Human blood cells are the only cells that HIV infects.
?(EURO)oeThis is an entirely new finding. It is a novel antibody that appears to be very effective in killing the HIV virus. The main question now is if this can be applied to developing vaccine and possibly used as a microbicide to prevent sexual transmission,?(EURO) said David C. Montefiori, Ph.D., director of the Laboratory for AIDS Vaccine Research & Development at Duke University Medical Center.
The abzymes are now under development for HIV immunotherapy by infusion into blood. They could also be used to guard against sexual HIV transmission as topical vaginal or rectal formulations.
The journal article is titled ?(EURO)oeCatalytic antibodies to HIV: Physiological role and potential clinical utility?(EURO) and is published in the latest issue of the journal Autoimmunity Reviews.
Published by HT Syndication with permission from Asian News International.
HINDUSTAN TIMES
May 20, 2008 Tuesday 2:20 PM EST
Modified blood-clotting protein may help people with hemophilia
BYLINE: Report from Asian News International brought to you by HT Syndication.
LENGTH: 373 words
DATELINE: WashingtonWashington, May 20 — Researchers at the University of Texas Health Science Center at Houston including an Indian boffin have developed a chemically modified protein that might help people with a hard-to-treat form of a genetic bleeding disorder known as Hemophilia A.
With lack of blood-clotting protein Factor VIII (FVIII), people with Hemophilia A typically receive injections of FVIII derived from plasma or produced synthetically to control potentially life-threatening episodes of bleeding.
However, as many as 1 in 3 people with Hemophilia A produce inhibitor antibodies, which attack the externally administered FVIII and negate its blood-clotting benefits.
To fight this problem, senior author Sudhir Paul, Ph.D., at The University of Texas Medical School at Houston and colleagues developed a chemically modified version of FVIII, which during laboratory tests neutralized these inhibitor antibodies, thus paving the way for the correction of the blood-coagulating process.
The modification is called electrophilic FVIII analog (E-FVIII).
“It’s a two-step process. The E-FVIII permanently inactivates the antibodies that inhibit blood clotting in 20 to 30 percent of patients receiving Factor VIII replacement therapy. Once the antibodies are cleared, additional FVIII can be injected,” Paul said.
The study, led by Stephanie Planque, involved blood donated by eight people with FVIII-resistant Hemophilia A.
Co-author Keri Smith, Ph.D., an assistant professor of pathology and laboratory medicine at the UT Medical School at Houston, said that today, people with FVIII-resistant Hemophilia A have limited treatment options.
Those options include bypass therapy or multiple FVIII injections. Both are prohibitively expensive and often ineffective to meet emergency blood-clotting needs.
Smith said that E-FVIII might provide a more economically feasible method of treating inhibitor antibodies.
According to Paul, the next step involves clinical trials.
“E-FVIII is a first generation reagent. Future genetic and chemical manipulations may help develop improved E-FVIII analogs,” Paul said.
The study appears in the May 2 issue of the Journal of Biological Chemistry.
Published by HT Syndication with permission from Asian News International.
