COMPLEMENT AND ANTIBODY MEDIATE ENHANCEMENT OF HIV-INFECTION BY INCREASING VIRUS BINDING AND PROVIRUS FORMATION

被引:53
作者
JUNE, RA
SCHADE, SZ
BANKOWSKI, MJ
KUHNS, M
MCNAMARA, A
LINT, TF
LANDAY, AL
SPEAR, GT
机构
[1] RUSH PRESBYTERIAN ST LUKES MED CTR,DEPT IMMUNOL MICROBIOL,1653 W CONGRESS PKWY,CHICAGO,IL 60612
[2] ABBOTT LABS,N CHICAGO,IL 60064
关键词
HIV; COMPLEMENT; CD4; PROVIRUS; ANTIBODY; COMPLEMENT RECEPTOR;
D O I
10.1097/00002030-199103000-00004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies have shown that infection of complement receptor (CR2)-bearing cells with HIV pretreated with antibody (Ab) plus complement (C) resulted in increased virus expression. The current study was designed to determine whether C-mediated 'enhancement' of HIV-1 production was the result of increased virus infection of cells as assessed by provirus formation and virus binding. Virus was incubated with anti-HIV Ab and/or C and added to CR2-positive MT-2 cells. Increased virus expression by MT-2 cells correlated with increased numbers of HIV-immunofluorescent-positive cells at 24 and 48 h and higher levels of provirus detected 8-28 h after infection. MT-2 cells also bound threefold more Ab-plus-C-treated virus than untreated virus. Serial dilutions of C showed that high levels of C with Ab did not enhance but rather suppressed virus expression. Studies were also performed which showed that terminal C components C5 and C8 were not necessary for the enhancing effect. The increased binding of C-coated HIV to CR-positive cells has important implications for the fate of virus in vivo.
引用
收藏
页码:269 / 274
页数:6
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