Gautreaux M D, Gelder F B, Deitch E A, Berg R D
Department of Microbiology and Immunology, Louisiana State University Medical Center-Shreveport, Shreveport 71130-3932, USA.
Infect Immun. 1995 Oct;63(10):3827-34. doi: 10.1128/iai.63.10.3827-3834.1995.
Bacterial translocation is defined as the passage of viable bacteria from the gastrointestinal (GI) tract to extraintestinal sites, such as the mesenteric lymph node (MLN), spleen, liver, kidneys, and blood. Previously, we reported that depletion of CD4+ and/or CD8+ T cells promotes bacterial translocation from the GI tract to the MLN. In the present study, CD4+ and/or CD8+ T cells, harvested from donor mice, were adoptively transferred to mice previously depleted of T cells by thymectomy plus intraperitoneal injection of rat anti-mouse T-cell monoclonal antibodies. The adoptively transferred CD4+ and/or CD8+ T cells inhibited the translocation of Escherichia coli from the GI tract. Migration of the adoptively transferred T cells to the spleens and MLNs of the recipient mice was determined by utilizing Thy 1.1+ donor cells adoptively transferred into mice whose cells express the Thy 1.2 marker. These results provide further evidence of the importance of T cells in the host immune defense against bacterial translocation from the GI tract.
细菌移位被定义为活细菌从胃肠道转移至肠外部位,如肠系膜淋巴结、脾脏、肝脏、肾脏和血液。此前,我们报道过CD4⁺和/或CD8⁺T细胞的缺失会促进细菌从胃肠道向肠系膜淋巴结的移位。在本研究中,从供体小鼠获取的CD4⁺和/或CD8⁺T细胞被过继转移至先前通过胸腺切除加腹腔注射大鼠抗小鼠T细胞单克隆抗体而耗尽T细胞的小鼠体内。过继转移的CD4⁺和/或CD8⁺T细胞抑制了大肠杆菌从胃肠道的移位。利用过继转移至表达Thy 1.2标记的小鼠体内的Thy 1.1⁺供体细胞,确定了过继转移的T细胞向受体小鼠脾脏和肠系膜淋巴结的迁移。这些结果进一步证明了T细胞在宿主针对胃肠道细菌移位的免疫防御中的重要性。