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Science 10 October 1997: Vol. 278. no. 5336, pp. 290 - 294 DOI: 10.1126/science.278.5336.290
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Reports
Angiogenic and HIV-Inhibitory Functions of KSHV-Encoded Chemokines
Chris Boshoff,
*
Yoshio Endo,
Paul D. Collins,
Yasuhiro Takeuchi,
Jacqueline D. Reeves,
Vicki L. Schweickart,
Michael A. Siani,
Takuma Sasaki,
Timothy J. Williams,
Patrick W. Gray,
Patrick S. Moore,
Yuan Chang,
Robin A. Weiss
Unique among known human herpesviruses, Kaposi's
sarcoma-associated herpesvirus (KSHV or HHV-8) encodes chemokine-like
proteins (vMIP-I and vMIP-II). vMIP-II was shown to block infection of human immunodeficiency virus-type 1 (HIV-1) on a CD4-positive cell
line expressing CCR3 and to a lesser extent on one expressing CCR5,
whereas both vMIP-I and vMIP-II partially inhibited HIV infection of
peripheral blood mononuclear cells. Like eotaxin, vMIP-II activated and
chemoattracted human eosinophils by way of CCR3. vMIP-I and vMIP-II,
but not cellular MIP-1 or RANTES, were highly angiogenic in the
chorioallantoic assay, suggesting a possible pathogenic role in
Kaposi's sarcoma.
C. Boshoff, Y. Takeuchi, J. D. Reeves, R. A. Weiss,
Institute of Cancer Research, Chester Beatty Laboratories, London SW3
6JB, UK.
Y. Endo and T. Sasaki, Department of Experimental Therapeutics and
Development Center for Molecular Target Drugs, Cancer Research
Institute, Kanazawa University, Japan.
P. D. Collins and T. J. Williams, Department of Applied
Pharmacology, Imperial College School of Medicine at National Heart and
Lung Institute, London SW3 6LY, UK.
V. L. Schweickart and P. W. Gray, ICOS, 22021 20th
Avenue Southeast, Bothell, WA 98021, USA.
M. A. Siani, Gryphon Sciences, San Francisco, CA 94080, USA.
P. S Moore and Y. Chang, Department of Pathology and Epidemiology,
College of Physicians and Surgeons of Columbia University, New York, NY
10032, USA.
*
To whom correspondence should be addressed.
Read the Full Text
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