gp41 Envelope Protein of Human Immunodeficiency Virus Induces Interleukin (IL)-10 in Monocytes, but Not in B, T, or NK Cells, Leading to Reduced IL-2 and Interferon-γ Production

The effect of extracellular domain of human immunodeficiency virus (HIV-1) transmembrane glycoprotein gp41 on interleukin (IL)-10, IL-2, interferon (IFN)-γ, IL-4, and tumor necrosis factora production by human peripheral blood mononuclear cells (PBMC) was assessed by ELISA. Rapid gp41-induced increa...

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Published in:The Journal of infectious diseases Vol. 177; no. 4; pp. 905 - 913
Main Authors: Barcova, Maria, Kacani, Laco, Speth, Cornelia, Dierich, Manfred P.
Format: Journal Article
Language:English
Published: Chicago, IL The University of Chicago Press 01-04-1998
University of Chicago Press
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Summary:The effect of extracellular domain of human immunodeficiency virus (HIV-1) transmembrane glycoprotein gp41 on interleukin (IL)-10, IL-2, interferon (IFN)-γ, IL-4, and tumor necrosis factora production by human peripheral blood mononuclear cells (PBMC) was assessed by ELISA. Rapid gp41-induced increase of IL-10 production was detected in resting PBMC and isolated monocytes but not in B, T, or NK cells. Furthermore, gp41 also enhanced IL-10 production in staphylococcal enterotoxin B-stimulated PBMC, while synthesis of IL-2, IFN-γ, and IL-4 in these cells was downmodulated. Kinetic studies revealed that increased IL-10 production preceded reduction of IL-2, indicating the possible IL-10 regulatory role in the gp41-induced down-modulation of this cytokine. Anti-IL-10 antibody reversed almost completely the gp41 inhibitory effect on IL-2 production. In this study, HIV-1 gp41 was a potent modulator of cytokine production by PBMC, in particular by increasing IL-10 secretion from normal monocytes/macrophages and consequently down-regulating IL-2 and IFN-γ.
Bibliography:ark:/67375/HXZ-SHX8051P-P
Reprints or correspondence: Dr. Manfred P. Dierich, Institute for Hygiene, University of Innsbruck, Fritz-Pregl-Str. 3, A-6020 Innsbruck, Austria.
istex:32D23BCD7056432BD46382D02BFC782FF42E5312
Presented in part: XXII Meeting of the European Tumor Virus Group, Innsbruck/Igls, Austria, 5–9 March 1997 (abstract 8/2).
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ISSN:0022-1899
1537-6613
DOI:10.1086/515230