This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. Studies in HIV-infected humans demonstrate that a 10-fold reduction in viremia reduces the death rate from 50% to 5% and prolongs survival time from less than 5 years to greater than 10 years. There is a great need to develop a safe and effective HIV/AIDS therapy that requires short-term intervention and long-term viral control. Here, we propose to evaluate the safety and therapeutic potential of in vivo blockade of the inhibitory receptor Programmed Death-1 (PD-1) as a novel therapy to control HIV/AIDS using a SIV/macaque model. We are testing the safety and therapeutic potential of in vivo PD-1 blockade in combination with vaccination in SIV-infected macaques. We hypothesize that combining PD-1 blockade with anti-retroviral therapy and vaccination will further improve the efficacy of in vivo PD-1 blockade by inducing a robust polyfunctional anti-viral cellular and humoral immunity that is capable of controlling the reemerging viremia following treatment interruption. The vaccine we use is a SIV239 DNA/MVA vaccine and it elicits high frequencies of CD8 and CD4 T cells in uninfected macaques. Blocking Ab is administered prior to or during vaccination. Correlations are conducted to identify immune responses that are critical for viral control. Our goal is to reduce the set point viremia at least by 50-100 fold. If successful, this therapy would potentially improve the health of more than 30 million HIV-infected people across the world. We infected macaques with SIV and initiated anti-retroviral therapy. We are in the process of vaccinating these animals in the presence of PD-1 blockade.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
2P51RR000165-51
Application #
8357496
Study Section
Special Emphasis Panel (ZRR1-CM-5 (01))
Project Start
2011-08-01
Project End
2012-04-30
Budget Start
2011-08-01
Budget End
2012-04-30
Support Year
51
Fiscal Year
2011
Total Cost
$74,294
Indirect Cost
Name
Emory University
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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