首页> 外文期刊>The Journal of Experomental Medicine >Intrarectal transmission, systemic infection, and CD4+ T cell depletion in humanized mice infected with HIV-1
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Intrarectal transmission, systemic infection, and CD4+ T cell depletion in humanized mice infected with HIV-1

机译:HIV-1感染的人源化小鼠的直肠内传播,全身感染和CD4 + T细胞耗竭

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Intrarectal infection between men who have sex with men represents a predominant form of human immunodeficiency virus (HIV) transmission in developed countries. Currently there are no adequate small animal models that recapitulate intrarectal HIV transmission. Here we demonstrate that human lymphocytes generated in situ from hematopoietic stem cells reconstitute the gastrointestinal tract of humanized mice with human CD4+ T cells rendering them susceptible to intrarectal HIV transmission. HIV infection after a single intrarectal inoculation results in systemic infection with depletion of CD4+ T cells in gut-associated lymphoid tissue and other pathologic sequela that closely mimics those observed in HIV infected humans. This novel model provides the basis for the development and evaluation of novel approaches aimed at immune reconstitution of human gut-associated lymphoid tissue and for the development, testing, and implementation of microbicides to prevent intrarectal HIV-1 transmission.
机译:与男性发生性关系的男性之间的直肠内感染是发达国家中人类免疫缺陷病毒(HIV)传播的主要形式。目前,没有足够的小动物模型可以概括直肠内HIV的传播。在这里,我们证明了从造血干细胞原位产生的人类淋巴细胞与人类CD4 + T细胞一起重组了人源化小鼠的胃肠道,使其易于直肠内HIV传播。一次直肠内接种后的HIV感染导致全身感染,肠道相关淋巴组织和其他病理后遗症中CD4 + T细胞耗竭,这些后遗症与在HIV感染者中观察到的情况非常相似。该新模型为开发和评估旨在人类肠道相关淋巴组织免疫重建的新方法以及开发,测试和实施预防直肠​​内HIV-1传播的杀微生物剂提供了基础。

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