This IPCP-HTM application made in response to RFA Al-oy-ooi contains three Research Projects, oneScientific Core and an Administrative Core, under the direction of Principal Investigator, John P. Moore,PhD and co-Principal Investigator, Robin A. Shattock, PhD. The purpose of the program is to conduct invitro and in vivo pre-clinical and animal model-based research intended to facilitate the development of avaginal microbicide based on the use of inhibitors of HIV-i entry, applied alone and/or in combination.Our goal is to use our collective knowledge of virology, immunology, formulation chemistry andmammalian biology to help develop a mechanism-based, HIV-i-specific microbicide(s). An emphasis willbe the development and evaluation of long-lasting microbicide formulations and delivery methods, such ascontrolled release vaginal rings that can provide a continuous and constant supply of active compounds insitu for a period of weeks/months after the application of a single device, and semi-solid formulations thatcould be applied once-daily or even less frequently. The inhibitors that we will study include, but may notbe limited to: the small molecule CCRs inhibitor, CMPDi67 (Merck); the small molecule attachmentinhibitor BMS-C (Bristol-Myers Squibb); the small molecule CXCR4 inhibitor AMD3465 (AnorMED); thegp4i-based peptide fusion inhibitor, T-1249 (Trimeris). We propose: Research Project I: Robin Shattock,Characterization of entry inhibitors in human cervical and rectal tissue models, and in dendritic cells;Research Project II: Karl Malcolm, Practical Formulations of HIV-i Entry Inhibitors; Research Project III:Ronald Veazey, Testing practical microbicides in macaques; Virology and Immunology Core: John P.Moore; Administrative Core: John P. Moore. Other senior members of the team include Melissa Robbianiand Mark Mitchnick (Particle Sciences, Inc) who will participate in Research Projects I and III,respectively, under Cooperative Agreements, and Steven Wolinsky who will take part in the Virology andImmunology Core, also under a Cooperative Agreement. The involvement of Particle Sciences fulfills themandated corporate element of the proposed research program. If this application is successfully peerreviewedand approved for support by the NIH, the International Partnership for Microbicides willprovide the majority of the funding required to support the research programs headed by Drs. Shattock,Robbiani and Wolinsky, as outlined in the Program Overview section of the application.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
1U19AI076982-01
Application #
7697230
Study Section
Special Emphasis Panel (ZAI1-CCH-A (S1))
Project Start
2008-09-20
Project End
2009-05-31
Budget Start
2008-06-23
Budget End
2009-05-31
Support Year
1
Fiscal Year
2008
Total Cost
$1,199,493
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
DUNS #
060217502
City
New York
State
NY
Country
United States
Zip Code
10065
Veazey, Ronald S; Ling, Binhua (2017) Short Communication: Comparative Susceptibility of Rhesus Macaques of Indian and Chinese Origin to Vaginal Simian-Human Immunodeficiency Virus Transmission as Models for HIV Prevention Research. AIDS Res Hum Retroviruses 33:1199-1201
Fletcher, Patricia; Herrera, Carolina; Armanasco, Naomi et al. (2016) Short Communication: Limited Anti-HIV-1 Activity of Maraviroc in Mucosal Tissues. AIDS Res Hum Retroviruses 32:334-8
Malcolm, R Karl; Lowry, Deborah; Boyd, Peter et al. (2014) Pharmacokinetics of a CCR5 inhibitor in rhesus macaques following vaginal, rectal and oral application. J Antimicrob Chemother 69:1325-9
Forbes, Claire J; McCoy, Clare F; Murphy, Diarmaid J et al. (2014) Modified silicone elastomer vaginal gels for sustained release of antiretroviral HIV microbicides. J Pharm Sci 103:1422-32
Fetherston, Susan M; Geer, Leslie; Veazey, Ronald S et al. (2013) Partial protection against multiple RT-SHIV162P3 vaginal challenge of rhesus macaques by a silicone elastomer vaginal ring releasing the NNRTI MC1220. J Antimicrob Chemother 68:394-403
Veazey, Ronald S (2013) Animal models for microbicide safety and efficacy testing. Curr Opin HIV AIDS 8:295-303
Malcolm, R Karl; Forbes, Claire J; Geer, Leslie et al. (2013) Pharmacokinetics and efficacy of a vaginally administered maraviroc gel in rhesus macaques. J Antimicrob Chemother 68:678-83
Johnson, Lisa M; Mortenson, David E; Yun, Hyun Gi et al. (2012) Enhancement of ýý-helix mimicry by an ýý/ýý-peptide foldamer via incorporation of a dense ionic side-chain array. J Am Chem Soc 134:7317-20
Ketas, Thomas J; Holuigue, Sophie; Matthews, Katie et al. (2012) Env-glycoprotein heterogeneity as a source of apparent synergy and enhanced cooperativity in inhibition of HIV-1 infection by neutralizing antibodies and entry inhibitors. Virology 422:22-36
Pessi, Antonello; Langella, Annunziata; Capito, Elena et al. (2012) A general strategy to endow natural fusion-protein-derived peptides with potent antiviral activity. PLoS One 7:e36833

Showing the most recent 10 out of 25 publications