Therapeutic interventions have so far failed to prevent or control infection with the human immunodeficiency virus (HIV). Development of novel strategies requires a multidisiplinary effort including individuals skilled in a broad range of the medical sciences. The major strength of the AECOM Center for AIDS Research (CFAR) rests up on its history of highly interactive research in general and in AIDS in particular. Expert researchers ar AECoM have focused for years on the study of HIv infection in and its effect on fetuses infants and pregnant women our investigations have lead to the identification of patients with unusually benign disease course and of the possible mechanisms of immune surveillance interfering with transplacental transmission of HIV. These findings are the key for the proposed research on molecular and immune interdiction of AIDS. In a concerted effort of clinical investigations and basic sciences, we will focus on several areas: (1) Identification and development of optimized human and murine neutralizing antibodies; (2) Antiidiotypes and mycobacterial vectors for AIDS vaccines; (3) Interference with the HIv replication cycle through cellular regulatory mechanisms of HIv expression; (4) Cellular and molecular analysis of HIv replication in the nervous system utilizing cell lines, organotypic cultures and brain tissues from fetuses. children and adults; (5) Molecular characterization of Toxoplasmosis in AIDs. The interdisciplinary collaboration will be fostered through several shared facilities: (1) The renovation of ample space for a centralized administrative and coordinative clinical and basic research core (Mazer). This facility will also house a centralized data management and AIDS-designated conference rooms; (2) Development of shared research core facilities including: Flow cytometry; Hybridoma facility; oligonucleotide and peptide synthesizing facility; (3) Funds are allocated for two new investigators, new initiatives and for crisis support to enhance novel ideas and ensure continuity of research efforts. The CFAR participating AECOM investigators are highly interactive through departmental affiliations, membership in the AIDS Research program and in the Cancer Center. They include nationally recognized clinical researchers and scientists, three of whom are members of the National Academy of Science.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Center Core Grants (P30)
Project #
5P30AI027741-02
Application #
3101048
Study Section
(SRC)
Project Start
1988-09-30
Project End
1993-08-31
Budget Start
1989-09-01
Budget End
1990-08-31
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Rubinstein, Arye (2005) Preclinical studies of alkylureas as anti-HIV-1 contraceptive. Curr Pharm Des 11:3769-78
Lenz, J; Su, M; Mizrachi, Y et al. (2001) V3 variation in HIV-seropositive patients receiving a V3- targeted vaccine. AIDS 15:577-81
Browning Paul, J; Wang, E J; Pettoello-Mantovani, M et al. (2000) Mice transgenic for monocyte-tropic HIV type 1 produce infectious virus and display plasma viremia: a new in vivo system for studying the postintegration phase of HIV replication. AIDS Res Hum Retroviruses 16:481-92
Rubinstein, A; Mizrachi, Y; Bernstein, L et al. (2000) Progressive specific immune attrition after primary, secondary and tertiary immunizations with bacteriophage phi X174 in asymptomatic HIV-1 infected patients. AIDS 14:F55-62
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Rubinstein, A; Mizrachi, Y; Pettoello-Mantovani, M et al. (1999) Immunologic responses of HIV-1-infected study subjects to immunization with a mixture of peptide protein derivative-V3 loop peptide conjugates. J Acquir Immune Defic Syndr 22:467-76
Pettoello-Mantovani, M; Kollmann, T R; Katopodis, N F et al. (1998) thy/liv-SCID-hu mice: a system for investigating the in vivo effects of multidrug therapy on plasma viremia and human immunodeficiency virus replication in lymphoid tissues. J Infect Dis 177:337-46
Landor, M; Rubinstein, A; Kim, A et al. (1998) Receptor-mediated maternofetal transfer of immunoglobulins. Inhibition of transport of anti-HIV-1 immunoglobulin by generic immunoglobulins in the in vitro perfused placenta. Int Arch Allergy Immunol 115:203-9
Browning, J; Horner, J W; Pettoello-Mantovani, M et al. (1997) Mice transgenic for human CD4 and CCR5 are susceptible to HIV infection. Proc Natl Acad Sci U S A 94:14637-41
Harish, Z; Rubinstein, A; Golodner, M et al. (1997) Suppression of HIV-1 replication by propolis and its immunoregulatory effect. Drugs Exp Clin Res 23:89-96

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