Angiogenic and HIV-inhibitory functions of KSHV-encoded chemokines

被引:391
作者
Boshoff, C
Endo, Y
Collins, PD
Takeuchi, Y
Reeves, JD
Schweickart, VL
Siani, MA
Sasaki, T
Williams, TJ
Gray, PW
Moore, PS
Chang, Y
Weiss, RA
机构
[1] KANAZAWA UNIV,DEPT EXPT THERAPEUT,KANAZAWA,ISHIKAWA 920,JAPAN
[2] KANAZAWA UNIV,DEV CTR MOL TARGET DRUGS,CANC RES INST,KANAZAWA,ISHIKAWA 920,JAPAN
[3] NATL HEART & LUNG INST,IMPERIAL COLL SCH MED,DEPT APPL PHARMACOL,LONDON SW3 6LY,ENGLAND
[4] ICOS,BOTHELL,WA 98021
[5] GRYPHON SCI,SAN FRANCISCO,CA 94080
[6] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PATHOL & EPIDEMIOL,NEW YORK,NY 10032
基金
英国惠康基金;
关键词
D O I
10.1126/science.278.5336.290
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 alpha or RANTES, were highly angiogenic in the chorioallantoic assay, suggesting a possible pathogenic role in Kaposi's sarcoma.
引用
收藏
页码:290 / 294
页数:5
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