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PMID: 1352911 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Programmed death of T cells in HIV-1 infection.

Science (New York, N.Y.) ·Vol. 257 ·No. 5067 ·1992-07-10 ·Pages 217-9

Meyaard L, Otto SA, Jonker RR, Mijnster MJ, Keet RP, Miedema F

Abstract

In human immunodeficiency virus (HIV) infection, functional defects and deletion of antigen-reactive T cells are more frequent than can be explained by direct viral infection. On culturing, both CD4+ and CD8+ T cells from asymptomatic HIV-infected individuals died as a result of programmed cell death (apoptosis). Apoptosis was enhanced by activation with CD3 antibodies. Programmed cell death, associated with impaired T cell reactivity, may thus be responsible for the deletion of reactive T cells that contributes to HIV-induced immunodeficiency.

MeSH Terms
Acquired Immunodeficiency Syndrome/pathology Antigens, CD/physiology CD4-Positive T-Lymphocytes/pathology CD8 Antigens/immunology Cell Death/physiology Cell Division/immunology Cells, Cultured HIV Envelope Protein gp120/physiology HIV-1 Humans Male Microscopy, Electron T-Lymphocytes/pathology Zinc/pharmacology
Chemicals
Antigens, CD CD8 Antigens HIV Envelope Protein gp120 Zinc
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Meyaard L
Department of Clinical Viro-Immunology, Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, Amsterdam.
Otto S A
Jonker R R
Mijnster M J
Keet R P
Miedema F
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1992-07-10
Pages
217-9
Language
English
Region
United States
NLM ID
0404511
Subset
IM
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