CD8+ T cell-mediated enhancement of tumour necrosis factor-alpha (TNF-α) production and HIV-1 LTR-driven gene expression in human monocytic cells is pertussis toxin-sensitive

被引:0
|
作者
Copeland, KFT
McKay, PJ
Newton, J
Rosenthal, KL
机构
[1] Ottawa Gen Hosp, Res Inst, Ctr Mol Med, Ottawa, ON K1H 8L6, Canada
[2] McMaster Univ, Hlth Sci Ctr, Dept Pathol & Mol Med, Hamilton, ON, Canada
来源
CLINICAL AND EXPERIMENTAL IMMUNOLOGY | 1999年 / 116卷 / 03期
关键词
HIV; CD8(+) T cell; macrophage; transcription; pertussis toxin;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
HIV replication and LTR-mediated gene expression can be modulated by CD8(+) T cells in a cell type-dependent manner. We have previously shown that supernatants of activated CD8(+) T cells of HIV-infected individuals greatly enhanced p24 levels in human macrophages infected with NSI or SI primary isolates of HIV-1. Here we have examined the effect of culture with CD8(+) T cell supernatants on HIV-1 LTR-mediated gene expression in monocytic cells. CD8(+) T cell supernatants enhanced LTR-mediated gene expression in U38 cells activated with Tat in the absence or presence of phorbol myristate acetate (PMA) and ionomycin or TNF-alpha. Further, enhancement of LTR-mediated gene expression and virus replication in U38 cells and U1 cells, respectively, was pertussis toxin-sensitive. The enhancement of gene expression and virus replication was associated with increased levels of TNF-alpha and was significantly abrogated by antibody to TNF-alpha. In contrast, the suppression of LTR-mediated gene expression by CD8(+) T cell supernatants in Jurkat T cells was not pertussis toxin-sensitive and TNF-alpha levels were not affected. These results demonstrate that factors produced by CD8(+) T cells utilize different cellular pathways to mediate their effects on HIV transcription and replication in different cell types.
引用
收藏
页码:479 / 485
页数:7
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