Quantitation of HIV-1-Specific Cytotoxic T Lymphocytes and Plasma Load of Viral RNA

Author:

Ogg Graham S.1234,Jin Xia1234,Bonhoeffer Sebastian1234,Dunbar P. Rod1234,Nowak Martin A.1234,Monard Simon1234,Segal Jeremy P.1234,Cao Yunzhen1234,Rowland-Jones Sarah L.1234,Cerundolo Vincenzo1234,Hurley Arlene1234,Markowitz Martin1234,Ho David D.1234,Nixon Douglas F.1234,McMichael Andrew J.1234

Affiliation:

1. G. S. Ogg, P. R. Dunbar, S. L. Rowland-Jones, V. Cerundolo, A. J. McMichael, Institute of Molecular Medicine, Nuffield Department of Medicine, Oxford OX3 9DS, UK.

2. X. Jin, S. Monard, J. P. Segal, Y. Cao, A. Hurley, M. Markowitz, D. D. Ho, D. F. Nixon, Aaron Diamond AIDS Research Center, 455 First Avenue, New York, NY 10016, USA.

3. S. Bonhoeffer, Aaron Diamond AIDS Research Center, 455 First Avenue, New York, NY 10016, USA, and Department of Zoology, University of Oxford, South Parks Road, Oxford OX13PS, UK.

4. M. A. Nowak, Department of Zoology, University of Oxford, South Parks Road, Oxford OX1 3PS, UK.

Abstract

Although cytotoxic T lymphocytes (CTLs) are thought to be involved in the control of human immunodeficiency virus–type 1 (HIV-1) infection, it has not been possible to demonstrate a direct relation between CTL activity and plasma RNA viral load. Human leukocyte antigen–peptide tetrameric complexes offer a specific means to directly quantitate circulating CTLs ex vivo. With the use of the tetrameric complexes, a significant inverse correlation was observed between HIV-specific CTL frequency and plasma RNA viral load. In contrast, no significant association was detected between the clearance rate of productively infected cells and frequency of HIV-specific CTLs. These data are consistent with a significant role for HIV-specific CTLs in the control of HIV infection and suggest a considerable cytopathic effect of the virus in vivo.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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