Donze H H, Cummins J E, Schwiebert R S, Kantele A, Han Y, Fultz P N, Jackson S, Mestecky J
Department of Microbiology, University of Alabama, Birmingham 35294, USA.
J Immunol. 1998 Mar 1;160(5):2506-13.
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.
在感染HIV-1的患者以及感染SIV的恒河猴中,均观察到肠道组织淋巴细胞浸润增加。为确定HIV-1和SIV感染是否影响人和非人灵长类外周血单个核细胞(PBMC)归巢至肠道组织,我们将人和非人灵长类PBMC移植到重症联合免疫缺陷(SCID)小鼠体内,并用无细胞或细胞相关的HIV-1或SIV感染它们。在同时接受PBMC和病毒的小鼠中,在肠道组织中发现了人或非人灵长类CD2⁺ T细胞,主要存在于上皮内淋巴细胞区和固有层。免疫磁珠分选显示这些细胞来源于CD4⁺群体。使用gag特异性引物,对这些组织进行PCR分析检测到HIV-1前病毒DNA的存在。然而,在移植了人或非人灵长类PBMC但未感染HIV-1或SIV的SCID小鼠中,未在肠道组织中检测到CD2⁺ T细胞。这些结果表明,在SCID小鼠模型中,HIV-1和SIV可调节人和非人灵长类T细胞的迁移特性。