Báfica André, Scanga Charles A, Schito Marco L, Hieny Sara, Sher Alan
Immunobiology Section, National Institute of Allergy and Infectious Diseases and. Chemical Immunology Section, Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
J Immunol. 2003 Aug 1;171(3):1123-7. doi: 10.4049/jimmunol.171.3.1123.
Mycobacterial infection has been implicated as a possible factor in AIDS progression in populations where HIV-1 and Mycobacterium tuberculosis are coendemic. In support of this concept, we have previously shown that HIV-1-transgenic (Tg) mice infected with mycobacteria display enhanced viral gene and protein expression. In this study, we demonstrate that the induction of HIV-1 observed in this model is dependent on Toll-like receptor 2 (TLR2), a pattern recognition receptor known to be involved in mycobacteria-host interaction. Spleen cells from HIV-1-Tg mice deficient in TLR2 (Tg/TLR2(-/-)) were found to be completely defective in p24 production induced in response to live M. tuberculosis or Mycobacterium avium as well as certain mycobacterial products. Importantly, following in vivo mycobacterial infection, Tg/TLR2(-/-) mice failed to display the enhanced HIV-1 gag/env mRNA and p24 protein synthesis exhibited by wild-type Tg animals. Together, these results argue that TLR2 plays a crucial role in the activation of HIV-1 expression by mycobacterial coinfections.
在HIV-1和结核分枝杆菌共同流行的人群中,分枝杆菌感染被认为是艾滋病进展的一个可能因素。为支持这一观点,我们之前已表明,感染分枝杆菌的HIV-1转基因(Tg)小鼠表现出增强的病毒基因和蛋白表达。在本研究中,我们证明在该模型中观察到的HIV-1诱导依赖于Toll样受体2(TLR2),这是一种已知参与分枝杆菌与宿主相互作用的模式识别受体。发现来自TLR2缺陷的HIV-1-Tg小鼠(Tg/TLR2(-/-))的脾细胞,在响应活的结核分枝杆菌或鸟分枝杆菌以及某些分枝杆菌产物时,p24产生完全缺陷。重要的是,在体内分枝杆菌感染后,Tg/TLR2(-/-)小鼠未能表现出野生型Tg动物所呈现的HIV-1 gag/env mRNA和p24蛋白合成增强。总之,这些结果表明TLR2在分枝杆菌合并感染激活HIV-1表达中起关键作用。