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首页> 外文期刊>Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society >Editorial: Live or let die--does HIV exacerbate tuberculosis by attenuating M. tuberculosis-induced apoptosis?
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Editorial: Live or let die--does HIV exacerbate tuberculosis by attenuating M. tuberculosis-induced apoptosis?

机译:社论:生死攸关-HIV是否会通过减弱结核分枝杆菌诱导的细胞凋亡来加剧结核病?

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摘要

TB remains the leading cause of bacterial-mediated mortality with 9.2 million new cases of TB reported in 2006 [1]. The susceptibility of HIV+ individuals to TB has fueled the spread of tuberculous disease, and HIV is the single most powerful risk factor for the development of TB [1]. As such, dissecting the factors that promote susceptibility to TB in HIV+ individuals is an urgent priority. HIV+ individuals exhibit increased susceptibility to tuberculous disease even with relatively preserved CD4+ T lymphocyte counts [2, 3], and this risk remains high after effective anti-retroviral therapy and immune reconstitution [4, 5]. This is suggestive of an early and persistent defect in immunity to Mtb, which is independent of the overall total CD4+ T lymphocyte count. The nature of this defect is unknown but may reside in the Mtb-specific adaptive immune response, where it could be a result of quantitative or qualitative differences in T cell responses or alternatively, in the innate immune response.
机译:结核仍然是细菌介导的死亡率的主要原因,2006年报告了920万例新结核病例[1]。 HIV +个体对结核病的易感性推动了结核病的蔓延,HIV是结核病发展的最强大的单一危险因素[1]。因此,剖析在HIV +个人中促进结核病易感性的因素是当务之急。即使具有相对保留的CD4 + T淋巴细胞计数,HIV +个体对结核病的敏感性也增加了[2,3],并且在有效的抗逆转录病毒疗法和免疫重建后,这种风险仍然很高[4,5]。这表明对Mtb的免疫存在早期和持续性缺陷,这与总CD4 + T淋巴细胞总数无关。该缺陷的性质未知,但可能存在于Mtb特异性适应性免疫反应中,这可能是T细胞反应或先天免疫反应在数量或质量上存在差异的结果。

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