A multidisciplinary approach to the study of AID/Kaposi's sarcoma patients is described. Studies will be carried out to compare three types of patients to determine if they have the same basic disease state. The three groups of patients to be sutdied are: (1) homosexual males with AID and/or Kaposi's sarcoma, (2) presumably heterosexual Haitian males who appear to have a similar disease characterized by opportunistic infections and/or Kaposi's sarcoma, and (3) hemophiliacs who have been receiving large volumes of unsterlized blood products (factor VIII). Recently several cases of an AID-like illness have been described among such hemophiliacs. These groups of patients will be evaluated with respect to (1) immune function, (2) macrophage function, and (3) possible viral etiology. The regulation of the immune response in these patients will be examined by in depth studies in three areas: (1) the generation of immune suppressive factors by their peripheral blood mononuclear cells, (2) the generation of helper an/or suppressor activity in autologous mixed lymphocyte reaction and (3) the presence of circulating antigen-antibody complexes. Macrophage function will be examined in respect to: (1) intracellular microbicidal activity, (2) activation of macrophages by lymphokines, (3) differentiation of macrophages and (4) function of macrophages in granuloma formation. Viral studies include attempts to demonstrate the presence of viral DNA in lymph nodes from AID patients using human CMV, simian CMV, human EBV and Herpes-simplex virus and restriction enzyme cleaved DNA and multiple different cloned viral DNA fragments as probes. Expression of viral specific antigens in cells from AID patients and the ability of T-cells from AID patients to control the proliferation of EBV-infected cells will also be studied. Tissues from Kaposi's sarcoma patients will also be studied.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
5U01CA035018-03
Application #
3548357
Study Section
(SSS)
Project Start
1983-05-01
Project End
1986-04-30
Budget Start
1985-05-01
Budget End
1986-04-30
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Weill Medical College of Cornell University
Department
Type
Schools of Medicine
DUNS #
201373169
City
New York
State
NY
Country
United States
Zip Code
10065
Pape, J W; Stanback, M E; Pamphile, M et al. (1990) Prevalence of HIV infection and high-risk activities in Haiti. J Acquir Immune Defic Syndr 3:995-1001
Murray, H W; Scavuzzo, D A; Kelly, C D et al. (1988) T4+ cell production of interferon gamma and the clinical spectrum of patients at risk for and with acquired immunodeficiency syndrome. Arch Intern Med 148:1613-6
Deschamps, M M; Pape, J W; Verdier, R I et al. (1988) Treatment of candida esophagitis in AIDS patients. Am J Gastroenterol 83:20-1
Murray, H W; Scavuzzo, D A; Chaparas, S D et al. (1988) T lymphocyte responses to mycobacterial antigen in AIDS patients with disseminated Mycobacterium avium-Mycobacterium intracellulare infection. Chest 93:922-5
Murray, H W; Scavuzzo, D; Jacobs, J L et al. (1987) In vitro and in vivo activation of human mononuclear phagocytes by interferon-gamma. Studies with normal and AIDS monocytes. J Immunol 138:2457-62
Hillman, J; Russo, C; Weksler, M E et al. (1987) Evidence for an activated subpopulation of T8-bearing cells in male homosexuals with lymphadenopathy. Int Arch Allergy Appl Immunol 84:18-24
Pape, J W; Levine, E; Beaulieu, M E et al. (1987) Cryptosporidiosis in Haitian children. Am J Trop Med Hyg 36:333-7
DeHovitz, J A; Pape, J W; Boncy, M et al. (1986) Clinical manifestations and therapy of Isospora belli infection in patients with the acquired immunodeficiency syndrome. N Engl J Med 315:87-90
Pape, J W; Liautaud, B; Thomas, F et al. (1986) Risk factors associated with AIDS in Haiti. Am J Med Sci 291:4-7
Murray, H W; Hillman, J K; Rubin, B Y et al. (1985) Patients at risk for AIDS-related opportunistic infections. Clinical manifestations and impaired gamma interferon production. N Engl J Med 313:1504-10

Showing the most recent 10 out of 14 publications