Our laboratory has been engaged in biologic, molecular and serologic studies of the AIDS-associated retrovirus (ARV). They are aimed at understanding the virus so that effective antiviral therapy and a vaccine can be developed. These efforts have led to the identification of over 300 isolates from peripheral mononuclear cells (PMC), brain tissue, and many different body fluids. They have revealed several distinctions among isolates that can be measured and need to be further studied. We shall continue ep[idemiologic and biologic studies of ARV by isolating virus from individuals over extended periods of time and evaluating any changes in the virus that may occur after infection of the host. This aspect will be approached as well by using a molecular clone of the AIDS virus in in vitro and in vivo studies. The possible existence of multiple isolates of ARV in the same individual will also be studied since development of AIDS may depend on either selected or multiple types of ARV. The biologic effect of the virus that will be examined include replicating abilities in different cells, viral interference, sensitivity to neutralization, and the nature of the cytopathology induced in certain infected cells. Moreover, the nature of latent ARV infection will be investigated. We shall examine whether the """"""""repressed"""""""" virus can be activated by certain drugs, other viruses, graft versus host responses or other specific co-factors associated with AIDS. The results could explain the emergence of AIDS in some individuals after a long incubation period.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI024499-03
Application #
3137536
Study Section
(SSS)
Project Start
1987-04-01
Project End
1990-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
3
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Gulizia, R J; Levy, J A; Mosier, D E (1996) The envelope gp120 gene of human immunodeficiency virus type 1 determines the rate of CD4-positive T-cell depletion in SCID mice engrafted with human peripheral blood leukocytes. J Virol 70:4184-7
Mosier, D E; Gulizia, R J; MacIsaac, P D et al. (1993) Rapid loss of CD4+ T cells in human-PBL-SCID mice by noncytopathic HIV isolates. Science 260:689-92
Tang, S; Poulin, L; Levy, J A (1992) Lack of human immunodeficiency virus type 1 (HIV-1) replication and accumulation of viral DNA in HIV-1-infected T cells blocked in cell replication. J Gen Virol 73 ( Pt 4):933-9
Cheng-Mayer, C; Quiroga, M; Tung, J W et al. (1990) Viral determinants of human immunodeficiency virus type 1 T-cell or macrophage tropism, cytopathogenicity, and CD4 antigen modulation. J Virol 64:4390-8
Weiss, C D; Levy, J A; White, J M (1990) Oligomeric organization of gp120 on infectious human immunodeficiency virus type 1 particles. J Virol 64:5674-7
York-Higgins, D; Cheng-Mayer, C; Bauer, D et al. (1990) Human immunodeficiency virus type 1 cellular host range, replication, and cytopathicity are linked to the envelope region of the viral genome. J Virol 64:4016-20
Levy, J A (1989) The human immunodeficiency viruses. Detection and pathogenesis. Immunol Ser 44:159-229
Evans, L A; Thomson-Honnebier, G; Steimer, K et al. (1989) Antibody-dependent cellular cytotoxicity is directed against both the gp120 and gp41 envelope proteins of HIV. AIDS 3:273-6
Homsy, J; Meyer, M; Tateno, M et al. (1989) The Fc and not CD4 receptor mediates antibody enhancement of HIV infection in human cells. Science 244:1357-60
Cheng-Mayer, C; Iannello, P; Shaw, K et al. (1989) Differential effects of nef on HIV replication: implications for viral pathogenesis in the host. Science 246:1629-32

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