Human immunodeficiency virus type 1 attachment, coreceptor, and fusion inhibitors are active against both direct and trans infection of primary cells

被引:53
作者
Ketas, TJ
Frank, I
Klasse, PJ
Sullivan, BM
Gardner, JP
Spenlehauer, C
Nesin, M
Olson, WC
Moore, JP
Pope, M
机构
[1] Populat Council, Ctr Biomed Res, New York, NY 10021 USA
[2] Progen Pharmaceut Inc, Tarrytown, NY 10591 USA
[3] Cornell Univ, Weill Med Coll, Dept Microbiol & Immunol, New York, NY 10021 USA
[4] Cornell Univ, Weill Med Coll, Dept Pediat, New York, NY 10021 USA
[5] Univ London Imperial Coll Sci Technol & Med, Wright Fleming Inst, Jefferiss Res Trust Labs, London W2 1PG, England
关键词
D O I
10.1128/JVI.77.4.2762-2767.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Inhibitors of human immunodeficiency virus type I attachment (CD4-immunoglobulin G subclass 2), CCR5 usage (PRO 140), and fusion (T-20) were tested on diverse primary cell types that represent the major targets both for infection in vivo and for the inhibition of trans infection of target cells by virus bound to dendritic cells. Although minor cell-type-dependent differences in potency were observed, each inhibitor was active on each cell type and trans infection was similarly vulnerable to inhibition at each stage of the fusion cascade.
引用
收藏
页码:2762 / 2767
页数:6
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