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Thursday, September 24, 2009

Investigational Vaccine Shows Modest Potential For Protecting Against HIV Infection

This information was reprinted from kff.org with permission from the Henry J. Kaiser Family Foundation. You can view the entire Kaiser Daily Global Health Policy Report, search the archives, and sign up for email delivery. © Henry J. Kaiser Family Foundation. All rights reserved.

Thursday, September 24, 2009

For the first time, scientists say an investigational vaccine has modest potential for protecting people against HIV infection, the Associated Press reports. "The vaccine — a combination of two previously unsuccessful vaccines — cut the risk of becoming infected with HIV by ... 31 percent in the world's largest [HIV] vaccine trial of more than 16,000 volunteers in Thailand, researchers announced Thursday in Bangkok," the news service writes (Marchione/Casey, 9/24).

"'It's the first evidence that we could have a safe and effective preventive vaccine,' Colonel Jerome Kim of the U.S. Army," which sponsored the trial, said at a press conference, the Financial Times reports, adding, "Doctors said an actual vaccine was still some way away but the tests provided a valuable 'proof of concept'" (Johnston, 9/24). Other supporters of the trial include the National Institute of Allergy and Infectious Diseases (NIAID), the Thai Ministry of Public Health "and the patent-holders in the two parts of the vaccine, Sanofi-Pasteur and Global Solutions for Infectious Diseases," the New York Times reports (McNeil, 9/24).

For the study, "[t]he researchers enrolled volunteers in Thailand’s Chon Buri and Rayong provinces, which have the nation’s highest rates of HIV, according to the study Web site," Bloomberg writes. "Subjects were given four doses of the ALVAC vaccine [made by Sanofi-Pasteur] and two of the AIDSVAX shot [made by VaxGen, now owned by Global Solutions for Infectious Diseases] over six months, then monitored for three years. They were also given advice on safe sex" (Bennett, 9/24).

The New York Times adds: Approximately "half the 16,402 volunteers were given six doses of two vaccines in 2006 and half were given placebos. Of those who got placebos, 74 became infected, while only 51 of those who got the vaccines did" (9/24).

"The results were barely significant on statistical grounds, perplexing for scientific reasons and unanticipated by most researchers," the Washington Post writes. "Nevertheless, the first positive results for an [HIV] vaccine after two decades of experimentation was being called a milestone" (Brown, 9/24).

Bloomberg continues: "In another finding, the vaccine failed to reduce the amount of virus in the blood of subjects who became infected. Researchers had hoped that if the vaccine didn’t prevent infections, it would at least cut the virus to levels so low it couldn’t be transmitted. … The researchers don’t understand exactly how the vaccine prevented infections or why it didn’t reduce viral load (9/24).

"'The study results, representing a significant scientific advance, are the first demonstration that a vaccine can prevent HIV infection in a general adult population and are of great importance,' the Geneva-based World Health Organisation and the Joint United Nations Programme on HIV/AIDS (UNAIDS) said" in a statement, Reuters writes. "It remains to be seen if the two specific vaccine components in this particular regime would be applicable to other parts of the world with diverse host genetic backgrounds and different HIV subtypes driving different regional sub-epidemics," according to the WHO and UNAIDS, Reuters reports (Nebehay, 9/24).

The Telegraph writes, "The researchers have been careful to say the vaccine combination appears to have an effect on the HIV strain circulating in Thailand and it may not work on other strains elsewhere in the world" (Smith/Jamieson, 9/24).

The Washington Post includes comments by Anthony Fauci, director of NIAID, who said, "Conceptually, we now know a vaccine is possible. Whether the vaccine is going to look anything like this one I don't know. But at least we know it can be done" (9/24). The New York Times reports, "Fauci said that scientists would seldom consider licensing a vaccine less than 70 or 80 percent effective, but he added, 'If you have a product that’s even a little bit protective, you want to look at the blood samples and figure out what particular response was effective and direct research from there'" (9/24). A NIAID press release is available here (9/24).

"Mass-producing the vaccine, plus how to proceed with future studies, will be discussed among the governments, study sponsors and companies involved in the trial, Kim said. Scientists want to know how long protection will last, whether booster shots will be needed, and whether the vaccine helps prevent infection in gay men and injection drug users, since it was tested mostly in heterosexuals in the Thai trial," the AP reports (9/24).

BBC reports, "'This result is tantalisingly encouraging. The numbers are small and the difference may have been due to chance, but this finding is the first positive news in the AIDS vaccine field for a decade,' said Dr. Richard Horton, editor of the Lancet medical journal. 'We should be cautious, but hopeful. The discovery needs urgent replication and investigation'" (9/24). BERMANA.com reports that the study "will form an important foundation for further HIV vaccine development in Thailand in the future," Paijit Warachit, deputy health permanent secretary in Thailand, said (9/24).

The Washington Post adds: "Many details of the trial were not released Wednesday afternoon in briefings to reporters," leading some to some skepticism among health experts. "More information will be presented at an AIDS vaccine meeting in Paris later this fall" (9/24).

Science's blog, "Science Insider," also reports on some researchers' skepticism over the results of the clinical trial (Cohen, 9/24).

Saturday, September 5, 2009

Two New Antibodies Found To Cripple HIV: 'Achilles' Heel On Virus For AIDS Vaccine Researchers To Exploit


ScienceDaily (2009-09-05) -- Researchers have discovered two powerful new antibodies to HIV that reveal what may be an Achilles heel on the virus. Researchers will now try to exploit the newfound vulnerability on the virus to craft novel approaches to designing an AIDS vaccine. Moreover, the global collaboration and process that led to the discovery of the two new broadly neutralizing antibodies (bNAbs) are likely to produce more such antibodies, which may in turn reveal additional vulnerabilities of HIV, adding still more vitality to the effort to develop a vaccine against AIDS.

Read More here- http://www.sciencedaily.com/releases/2009/09/090903163730.htm

Saturday, June 27, 2009

Young, HIV-Positive, and Unaware

This was an eye opening article From Web MD. In the article they discuss the statistics of young adults unaware they were living with HIV in 2006. The numbers are frightening to think how many of these young people have unknowingly infected theirs partners with the HIV virus.
The article is here. Please encourage everyone to get tested. It is not just your health at risk!
Young, HIV-Positive, and Unaware

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Tuesday, November 18, 2008

Could We Reprogram Immune System To Beat HIV Without Bone Marrow Transplant From A Donor With An Anti-HIV Gene Configuration?

According to media reports this week, an American patient living in Germany and suffering with both leukemia and HIV was apparently cured of both conditions following a bone marrow transplant from a unique donor. The donor possessed a very rare genetic variation that makes it difficult for HIV to enter into his healthy cells. In essence, by transplanting bone marrow from this particular donor to the HIV positive patient, the patient developed a new immune system capable of fending off HIV.

Bone marrow transplants might not be the most efficacious, or comfortable, means of rebuilding an immune system that can contend with HIV. However, there are other means of reprogramming the immune system, and without putting the patient's life at greater risk. Vaccines offer one such approach, but one thus far proven ineffective and even detrimental for those at risk of contracting HIV. Vaccines reprogram the immune system by triggering it to generate antibodies to proteins, or antigens, on the surface of viruses.

Because HIV gets inside of healthy cells so fast, there is little time for the antibodies to do their part, diminishing the ultimate value of vaccines for this disease. The recent failure of Merck's vaccine, V520, in which the risk of contracting HIV increased after vaccination, is a testament to the limited utility of vaccines for HIV.

Fortunately, antibodies are not the only means of reprogramming the immune system.

To read More Click Here.
http://www.medicalnewstoday.com/articles/129797.php

Saturday, November 15, 2008

Toehold For HIV's Assault On Brain Identified


Toehold For HIV's Assault On Brain Identified

Posted on: Saturday, 15 November 2008, 08:57 CST

Scientists have unraveled in unprecedented detail the cascade of events that go wrong in brain cells affected by HIV, a virus whose assault on the nervous system continues unabated despite antiviral medications that can keep the virus at bay for years in the rest of the body.

The new research reveals key steps taken in the brain by Tat, a protein that is central to HIV's attack on cells called neurons. Researchers discovered the receptor that Tat uses to attack neurons, and they were able to reverse the effects of Tat in the laboratory by blocking the receptor.

The discovery of a major molecular player in the process opens up a new avenue for researchers to explore in their efforts to prevent or treat HIV's neurological effects, for which there is no currently approved treatment. Researchers say that much of the molecular action that underlies HIV's attack on the brain also occurs in other diseases, such as Parkinson's and Alzheimer's diseases, and that the results spell progress for those conditions as well.

To read the rest of the article at Red Orbit click here.

Friday, November 14, 2008

Genetic Immunity announces first patient dosed in trial with DermaVir patch for HIV


Genetic Immunity, a US/Hungarian clinical-stage company focused on development of nanomedicines for targeted immune amplification, today announced it has treated the first subject in a Phase II clinical study to evaluate DermaVir Patch.

DermaVir Patch, the Company's lead nanomedicine candidate for treatment-na? HIV-infected individuals, is designed to amplify de novo HIV-specific memory T-cell responses of HIV-infected individuals and improve the ability of their own immune system to control the disease.

To read the Entire at News-Medical.net article click here.