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PMID: 7734188 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cell surface phenotypic changes induced in H9 T cells chronically infected with HTLV type I or HIV type 1 or coinfected with the two viruses.

AIDS research and human retroviruses ·Vol. 11 ·No. 1 ·1995-01-00 ·Pages 145-54

Noraz N, Verrier B, Fraisier C, Desgranges C

Abstract

To investigate whether HTLV-I infection, HIV-I infection, or HIV-I infection of HTLV-I-infected cells affect the expression of cellular surface molecules, an HTLV-I-infected T cell line derived from the H9 T cell line was established (H36). H9 cells uninfected or infected with HTLV-I were then infected with HIV-1. We have compared the density of different surface markers on these three infected H9 T cell lines. These markers consist of T cell-specific antigens (CD2, CD3, CD4, and CD8), activated T cell antigens (CD25 and CD71), major histocompatibility complex (MHC) antigens (class I and II), and adhesion molecules (LFA-1 and ICAM-1). The experiments reported in this article show that chronic HTLV-I infection, HIV-1 infection, and HIV-1 infection of HTLV-I-infected T cells modulate the expression of several immunologically important cell surface antigens. The nature and the extent of T lymphoid cell phenotypic modulation depend on the infecting virus. Furthermore, HTLV-I and HIV-1 interact with each other in the phenotypic modulation of coinfected cells.

MeSH Terms
Antigens, CD/analysis Cell Adhesion Molecules/analysis Cell Line Cell Membrane/virology HIV Infections/metabolism HIV-1 HLA Antigens/analysis HTLV-I Infections/metabolism Humans Immunophenotyping T-Lymphocytes/metabolism,virology
Chemicals
Antigens, CD Cell Adhesion Molecules HLA Antigens
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Noraz N
INSERM U271, Lyon, France.
Verrier B
Fraisier C
Desgranges C
Article Info
Journal
AIDS research and human retroviruses
Abbr.
AIDS Res Hum Retroviruses
ISSN
0889-2229
Published
1995-01-00
Pages
145-54
Language
English
Region
United States
NLM ID
8709376
Subset
IM
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