Enhanced expression of CTLA-4 (CD152) on CD4+ T cells in HIV infection

Author:

STEINER K1,WAASE I2,RAU T3,DIETRICH M2,FLEISCHER B1,BRÖKER B M1

Affiliation:

1. Department of Immunology

2. Department of Clinical Medicine, Bernhard-Nocht-Institut für Tropenmedizin

3. Centre for Cardiology, Othmarschen, Hamburg, Germany

Abstract

SUMMARY CTLA-4 (CD152) is a surface molecule of activated T cells with sequence homology to CD28. Both molecules bind to the same ligands, B7.1 (CD80) and B7.2 (CD86) but have antagonistic functions. While CD28 is an important costimulator, CTLA-4 has an essential inhibitory function in maintaining the homeostasis of the immune system. Down- regulation of CD28 predominantly on CD8+ T cells has been described in HIV infection, but analysis of CTLA-4 is complicated by its low expression levels. Here we have used potent signal enhancement to study CTLA-4 on peripheral blood mononuclear cells (PBMC) during HIV infection. CTLA-4 was expressed only on T cells. Expression levels were significantly increased selectively on CD4+ T cells during all stages of HIV infection, while CTLA-4 expression on CD8+ T cells was always low. In contrast, after stimulation with the mitogen phytohaemagglutinin (PHA), CTLA-4 levels were strongly increased on T cells from controls but in T cells from HIV patients this response was severely impaired. Our data suggest that in HIV infection CD4+ and CD8+ T cells may be less responsive to B7 costimuli due to two different mechanisms: increase in CTLA-4 expression by CD4+ cells and down-regulation of CD28 by CD8+ cells.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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