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Slowing down immune system's 'brakes' could perk up HIV vaccines' efficacy

Washington, Fri, 26 Mar 2010 ANI

Washington, Mar 26 (ANI): Just like a frisky driver slams the break of a car, a special class of T cells may be limiting the effectiveness of therapeutic vaccines for HIV by slowing the immune system response too soon, according to researchers at University of Pittsburgh.


The study is the first to look at the role of regulatory T cells in therapeutic HIV vaccines and could help researchers to improve the efficacy of such vaccines by devising methods to circumvent the braking mechanism of these cells.


Regulatory T cells (Treg) are critical because they prevent the immune system from turning against itself by suppressing the immune response.


Without the braking action of Treg, autoimmune disease could flourish.


However, the researchers didn't know what would happen if these cells start shutting down the immune response before a therapeutic vaccine has had a chance to bolster immunity against HIV.


Pitt researchers sought to answer this question as follow-up to a clinical trial of a therapeutic dendritic cell-based HIV vaccine they developed to activate the CD8, or killer T cell, response.


First reported in 2008, the findings indicated only limited success of the vaccine in the 17 patients enrolled in the trial.


In the current study, the researchers went back to the freezer, removed Treg from the patients' blood cell samples and found that it was masking a two-fold increase in immune response to HIV induced by the vaccine.


"When we removed Treg from blood cells, we found a much stronger immune response to the vaccine, giving us insight into how we can develop more effective HIV vaccines," said Dr. Charles R. Rinaldo, Jr.


"Treg normally shuts down CD8 responses once the infection has been controlled, but in this case it appears to be putting on the brakes early and possibly limiting the vaccine's ability to do its job effectively," he added.


One theory is that HIV-infection drives up Treg, which in turn shuts down the HIV-1- specific CD8 T cell response, he said.


"We know how to treat HIV, but are still learning how to use immunotherapy strategies to completely flush it out of the body. Our findings show Treg plays an important role, but we need to figure out how to maintain the right balance by getting around these cells without blocking them completely," added Dr. Bernard J.C. Macatangay.


The study has been published in the current issue of PLoS ONE. (ANI)



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