HIV TYPE 1-SPECIFIC CYTOTOXIC T-LYMPHOCYTES STIMULATE HLA CLASS-I ANDINTERCELLULAR-ADHESION MOLECULE TYPE-1 EXPRESSION AND INCREASE BETA(2)-MICROGLOBULIN LEVELS IN-VITRO

Citation
C. Jassoy et al., HIV TYPE 1-SPECIFIC CYTOTOXIC T-LYMPHOCYTES STIMULATE HLA CLASS-I ANDINTERCELLULAR-ADHESION MOLECULE TYPE-1 EXPRESSION AND INCREASE BETA(2)-MICROGLOBULIN LEVELS IN-VITRO, AIDS research and human retroviruses, 10(12), 1994, pp. 1685-1693
Citations number
62
Categorie Soggetti
Immunology,"Infectious Diseases
ISSN journal
08892229
Volume
10
Issue
12
Year of publication
1994
Pages
1685 - 1693
Database
ISI
SICI code
0889-2229(1994)10:12<1685:HT1CTS>2.0.ZU;2-0
Abstract
Besides acting in a direct manner, cytolytic HIV-1-specific CTLs relea se a variety of cytokines. To assess the potential role of cytokines r eleased by these CTLs we tested the ability of soluble products secret ed by HTV-1-specific CTLs to induce HLA class I and ICAM-1 expression and to raise beta(2)-microglobulin (beta(2)M) concentrations in cell c ulture. To this end, supernatants were derived from HIV-1-specific CTL s incubated with autologous B lymphoblasts presenting either the cogna te HIV-1 epitope or a control peptide. Cell lines and peripheral blood mononuclear cells (PBMCs) were incubated with these supernatants for 24-48 hr. Similarly, cells were cocultured with CTLs and their targets . This study demonstrates that in parallel with lysis of their cognate target, HIV-1-specific CTLs secreted products that stimulated HLA cla ss I and ICAM-1 expression on cell lines and PBMCs. As few as 1000 CTL s significantly induced the expression of these molecules. In addition , secreted products of HIV-specific CTLs enhanced beta(2)M release by PBMCs and Jurkat cells. These effects were mediated primarily by IFN-g amma and suggest that HIV-specific CTLs may contribute to increased HL A class I expression in infected tissue and elevated ICAM-1 and beta(2 )M concentrations in serum and cerebrospinal fluid of infected individ uals.