Human Immunodeficiency Virus Type 1- and Cytomegalovirus-Specific Cytotoxic T Lymphocytes Can Persist at High Frequency for Prolonged Periods in the Absence of Circulating Peripheral CD4 + T Cells

Author:

Spiegel Hans M. L.1,Ogg Graham S.2,DeFalcon Elizabeth1,Sheehy Megan E.1,Monard Simon1,Haslett Patrick A. J.3,Gillespie Geraldine2,Donahoe Sean M.1,Pollack Henry4,Borkowsky William4,McMichael Andrew J.2,Nixon Douglas F.1

Affiliation:

1. Aaron Diamond AIDS Research Center, The Rockefeller University,1 and

2. Molecular Immunology Group, Nuffield Department of Medicine, Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford OX3 9DU, United Kingdom2; and

3. Laboratory of Cellular Physiology and Immunology, The Rockefeller University, New York, New York 10021-63993

4. Division of Pediatric Infectious Diseases, New York University Medical Center,4 New York, New York 10016;

Abstract

ABSTRACT CD4 + T cells are thought to be critical in the maintenance of virus-specific CD8 + cytotoxic T-cell (CTL) responses. In human immunodeficiency virus type 1 (HIV-1) infection, a selective decline in HIV-1-specific CTL as the CD4 + T-cell count decreases has been reported. Using HLA-peptide tetrameric complexes, we show the presence at high frequency of HIV-1- and cytomegalovirus-specific CD8 + T cells when the peripheral CD4 + T-cell count was low or zero in three HIV-1-infected patients. No direct virus-specific CD8 + -mediated effector activity was seen in these subjects, suggesting antigen unresponsiveness, although tetramer-sorted cells could be expanded in vitro in the presence of interleukin-2 into responsive effector cells. Thus, virus-specific CD8 + T cells can be maintained in the peripheral circulation at high frequency in the absence of circulating peripheral CD4 + T cells, but these cells may lack direct effector activity. Strategies designed to overcome this antigen unresponsiveness may be of value in therapies for the treatment of AIDS.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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