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PMID: 8023142 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Ability of HIV to promote a TH1 to TH0 shift and to replicate preferentially in TH2 and TH0 cells.

Science (New York, N.Y.) ·Vol. 265 ·No. 5169 ·1994-07-08 ·Pages 244-8

Maggi E, Mazzetti M, Ravina A, Annunziato F, de Carli M, Piccinni MP, Manetti R, Carbonari M, Pesce AM, del Prete G

Abstract

Both interferon gamma (IFN-gamma) produced by T helper 1 (TH1) lymphocytes and interleukin-4 (IL-4) produced by TH2 lymphocytes were reduced in either bulk circulating mononuclear cells or mitogen-induced CD4+ T cell clones from the peripheral blood of individuals infected with human immunodeficiency virus (HIV). There was a preferential reduction in clones producing IL-4 and IL-5 in the advanced phases of infection. However, enhanced proportions of CD4+ T cell clones producing both TH1-type and TH2-type cytokines (TH0 clones) were generated from either skin-infiltrating T cells that had been activated in vivo or peripheral blood T cells stimulated by antigen in vitro when cells were isolated from HIV-infected individuals. All TH2 and most TH0 clones supported viral replication, although viral replication was not detected in any of the TH1 clones infected in vitro with HIV. These results suggest that HIV (i) does not induce a definite TH1 to TH2 switch, but can favor a shift to the TH0 phenotype in response to recall antigens, and (ii) preferentially replicates in CD4+ T cells producing TH2-type cytokines (TH2 and TH0).

MeSH Terms
Acquired Immunodeficiency Syndrome/immunology Cell Line Cells, Cultured HIV/physiology HIV Infections/immunology,microbiology HIV Seropositivity/immunology Humans Immunologic Memory Interferon-gamma/biosynthesis Interleukin-4/biosynthesis Interleukin-5/biosynthesis Interleukins/biosynthesis Lymphocyte Activation Phenotype T-Lymphocytes, Helper-Inducer/immunology,microbiology Virus Replication
Chemicals
Interleukin-5 Interleukins Interleukin-4 Interferon-gamma
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Maggi E
Division of Clinical Immunology and Allergy, University of Florence, Italy.
Mazzetti M
Ravina A
Annunziato F
de Carli M
Piccinni M P
Manetti R
Carbonari M
Pesce A M
del Prete G
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1994-07-08
Pages
244-8
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Corrections
CommentIn
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