Inhibition of HIV-1 Infection by the β-Chemokine MDC

Author:

Pal Ranajit123,Garzino-Demo Alfredo123,Markham Phillip D.123,Burns Jennifer123,Brown Michelle123,Gallo Robert C.123,DeVico Anthony L.123

Affiliation:

1. R. Pal, P. D. Markham, M. Brown, Advanced BioScience Laboratories, 5510 Nicholson Lane, Kensington, MD 20895, USA.

2. A. Garzino-Demo, R. C. Gallo, A. L. DeVico, Institute of Human Virology, University of Maryland at Baltimore, 725 West Lombard Street, Baltimore, MD 21201–1192, USA.

3. J. Burns, Institute of Human Virology and Department of Microbiology and Immunology, University of Maryland School of Medicine, University of Maryland at Baltimore, 655 West Baltimore Street, Baltimore, MD 21201–1192, USA.

Abstract

CD8 + T lymphocytes from individuals infected with human immunodeficiency virus–type 1 (HIV-1) secrete a soluble activity that suppresses infection by HIV-1. A protein associated with this activity was purified from the culture supernatant of an immortalized CD8 + T cell clone and identified as the β-chemokine macrophage-derived chemokine (MDC). MDC suppressed infection of CD8 + cell–depleted peripheral blood mononuclear cells by primary non–syncytium-inducing and syncytium-inducing isolates of HIV-1 and the T cell line–adapted isolate HIV-1 IIIB . MDC was expressed in activated, but not resting, peripheral blood mononuclear cells and binds a receptor on activated primary T cells. These observations indicate that β-chemokines are responsible for a major proportion of HIV-1–specific suppressor activity produced by primary T cells.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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