Macrophage-dependent Apoptosis of CD4+ T Lymphocytes from HIV-infected Individuals Is Mediated by FasL and Tumor Necrosis Factor

Author:

Badley Andrew D.1,Dockrell David1,Simpson Margaret1,Schut Ron1,Lynch David H.1,Leibson Paul1,Paya Carlos V.111

Affiliation:

1. From the Division of Infectious Diseases, Division of Experimental Pathology, and Department of Immunology, Mayo Clinic, Rochester, Minnesota 55901; Division of Infectious Diseases, Hennepin County Medical Center, Minneapolis, Minnesota 55404; and Immunex Corporation, Seattle, Washington 98101

Abstract

Apoptosis of bystander uninfected CD4+ T lymphocytes by neighboring HIV-infected cells is observed in cell culture and in lymphoid tissue of HIV-infected individuals. This study addresses whether antigen-presenting cells such as human macrophages mediate apoptosis of CD4+ T cells from HIV-infected individuals. Uninfected human macrophages, and to a larger degree, HIV-infected macrophages mediate apoptosis of T cells from HIV-infected, but not from uninfected control individuals. This macrophage-dependent killing targets CD4+, but not CD8+ T lymphocytes from HIV-infected individuals, and direct contact between macrophages and lymphocytes is required. Additional analyses indicated that the apoptosis-inducing ligands, FasL and tumor necrosis factor (TNF), mediate this macrophage-induced apoptosis of CD4+ T cells. These results support a role for macrophage-associated FasL and TNF in the selective depletion of CD4+ T cells in HIV-infected individuals.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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