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HIV-1/Simian Immunodeficiency Virus Infection of Human and Nonhuman Primate Lymphocytes Results in the Migration of CD2+ T Cells into the Intestine of Engrafted SCID Mice

机译:人类和非人类灵长类动物淋巴细胞的HIV-1 / Simian免疫缺陷病毒感染导致CD2 + T细胞迁移到植入的SCID小鼠肠道中

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Increased lymphocytic infiltration of intestinal tissues has been observed in patients infected with HIV-1 and in SIV-infected rhesus macaques. To determine whether HIV-1 and SIV infections influence the homing of human and nonhuman primate PBMC to intestinal tissues, we engrafted SCID mice with human or nonhuman primate PBMC and infected them with either cell-free or cell-associated HIV-1 or SIV. In mice that received both PBMC and virus, human or nonhuman primate CD2+ T cells were found in intestinal tissues, primarily in the intraepithelial lymphocyte compartment and lamina propria. Immunomagnetic sorting revealed that these cells were derived from the CD4+ population. Using gag -specific primers, PCR analysis of these tissues detected the presence of HIV-1 proviral DNA. However, in SCID mice that were engrafted with either human or nonhuman primate PBMC and no HIV-1 or SIV, CD2+ T cells were not detected in intestinal tissues. These results indicate that HIV-1 and SIV can modulate the migratory properties of human and nonhuman primate T cells in the SCID mouse model.
机译:在感染了HIV-1的患者和感染SIV的恒河猴中,发现肠道组织的淋巴细胞浸润增加。为了确定HIV-1和SIV感染是否影响人类和非人类灵长类PBMC向肠道组织的归巢,我们将人类或非人类灵长类PBMC植入SCID小鼠,并用无细胞或与细胞相关的HIV-1或SIV感染它们。在同时接受PBMC和病毒的小鼠中,主要在上皮内淋巴细胞区和固有层的肠道组织中发现了人类或非人类的灵长类动物CD2 + T细胞。免疫磁性分选显示,这些细胞来自CD4 +群体。使用gag特异的引物,对这些组织的PCR分析检测到HIV-1前病毒DNA的存在。但是,在植入了人类或非人类灵长类PBMC且没有HIV-1或SIV的SCID小鼠中,在肠道组织中未检测到CD2 + T细胞。这些结果表明,HIV-1和SIV可以调节SCID小鼠模型中人类和非人类灵长类T细胞的迁移特性。

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