This Program Project constitutes three individual Research Projects, one Research Support Core and an Administrative Core, under the direction of Principal Investigator, John P. Moore, Ph.D. and co-investigator, Mark Wainberg, M.D.. The purpose of this program is to conduct in vitro and in vivo pre- clinical and animal model-based research intended to identify and characterize inhibitors of HIV-1 replication that might be suitable for commercial development as topical microbicides. The applicant?s central hypothesis is that specific inhibitors of HIV-1 attachment, fusion and entry could prevent or hinder the vaginal or rectal transmission of HIV-1, when properly formulated and applied to women or men prior to sexual intercourse. The applicant believes that microbicides should be designed and developed based on rational scientific principles, taking into account accumulated knowledge of the stages of the viral life cycle to be impeded, the mechanism of action of the candidate inhibitors, and the biological processes involved in HIV-1 transmission. The applicant does not intend to study microbicide candidates that have a non-specific mechanism of action, that have a broad-spectrum activity against multiple pathogens, or that are also spermicides. His goal is to use his collective knowledge of HIV-1 virology and mammalian biology to help develop a mechanism- based, HIV-l-specific microbicide(s). Towards this goal, the applicant has obtained and will comparatively evaluate in vitro and in vivo, both alone and in combination, several different inhibitors of defined stages in HIV-1 entry. Rather than focus on a single compound, the applicant seeks to identify the best inhibitor(s) to move into clinical development. He proposes: Research Project I: Robin Shattock, Ph.D., Characterization of HIV-1 fusion/entry inhibitors in human cervical and rectal tissue models; Research Project II: Melissa Pope, Ph.D., Assessment of fusion/entry inhibitors in DC-T cell mixtures; Research Project III: Ronald Veazey, Ph.D., Evaluation of fusion inhibitors for protection from SHIV and SIV vaginal or rectal challenge in macaques; Scientific Core: John P. Moore, Ph.D., Fusion-Inhibitor Acquisition, Evaluation and Formulation; Administrative Core: John P. Moore, Ph.D.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
1P01AI052048-01
Application #
6443182
Study Section
Special Emphasis Panel (ZHD1-DRG-D (18))
Program Officer
Black, Roberta J
Project Start
2001-09-30
Project End
2005-09-29
Budget Start
2001-09-30
Budget End
2002-09-29
Support Year
1
Fiscal Year
2001
Total Cost
$1,203,448
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Frank, Ines; Robbiani, Melissa (2011) Attachment and fusion inhibitors potently prevent dendritic cell-driven HIV infection. J Acquir Immune Defic Syndr 56:204-12
Frank, I; Stossel, H; Gettie, A et al. (2008) A fusion inhibitor prevents spread of immunodeficiency viruses, but not activation of virus-specific T cells, by dendritic cells. J Virol 82:5329-39
Veazey, Ronald S (2008) Microbicide safety/efficacy studies in animals: macaques and small animal models. Curr Opin HIV AIDS 3:567-73
Turville, Stuart G; Aravantinou, Meropi; Stossel, Hella et al. (2008) Resolution of de novo HIV production and trafficking in immature dendritic cells. Nat Methods 5:75-85
Hu, Qinxue; Younson, Justine; Griffin, George E et al. (2006) Pertussis toxin and its binding unit inhibit HIV-1 infection of human cervical tissue and macrophages involving a CD14 pathway. J Infect Dis 194:1547-56
Teleshova, N; Kenney, J; Robbiani, M (2006) Dendritic cells and HIV infection: activating dendritic cells to boost immunity. Adv Dent Res 19:36-41
Morcock, David R; Thomas, James A; Gagliardi, Tracy D et al. (2005) Elimination of retroviral infectivity by N-ethylmaleimide with preservation of functional envelope glycoproteins. J Virol 79:1533-42
Cilliers, Tonie; Willey, Samantha; Sullivan, W Mathew et al. (2005) Use of alternate coreceptors on primary cells by two HIV-1 isolates. Virology 339:136-44
Hu, Qinxue; Napier, Kelby B; Trent, John O et al. (2005) Restricted variable residues in the C-terminal segment of HIV-1 V3 loop regulate the molecular anatomy of CCR5 utilization. J Mol Biol 350:699-712
Turville, Stuart G; Santos, John J; Frank, Ines et al. (2004) Immunodeficiency virus uptake, turnover, and 2-phase transfer in human dendritic cells. Blood 103:2170-9

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