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Dynamics of T cell, antigen-presenting cell, and pathogen interactions during recall responses in the lymph node.

机译:在淋巴结的召回反应期间,T细胞,抗原呈递细胞和病原体相互作用的动力学。

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摘要

Memory T cells circulate through lymph nodes where they are poised to respond rapidly upon re-exposure to a pathogen; however, the dynamics of memory T cell, antigen-presenting cell, and pathogen interactions during recall responses are largely unknown. We used a mouse model of infection with the intracellular protozoan parasite, Toxoplasma gondii, in conjunction with two-photon microscopy, to address this question. After challenge, memory T cells migrated more rapidly than naive T cells, relocalized toward the subcapsular sinus (SCS) near invaded macrophages, and engaged in prolonged interactions with infected cells. Parasite invasion of T cells occurred by direct transfer of the parasite from the target cell into the T cell and corresponded to an antigen-specific increase in the rate of T cell invasion. Our results provide insight into cellular interactions during recall responses and suggest a mechanism of pathogen subversion of the immune response.
机译:记忆性T细胞通过淋巴结循环,在重新接触病原体时它们会迅速做出反应;然而,记忆T细胞,抗原呈递细胞和病原体相互作用在召回反应过程中的动力学是很大程度上未知。我们使用细胞内原生动物寄生虫弓形虫感染的小鼠模型,结合双光子显微镜技术,来解决这个问题。攻击后,记忆T细胞比幼稚T细胞迁移更快,重新定位到入侵的巨噬细胞附近的囊下窦(SCS),并与感染的细胞进行长时间的相互作用。 T细胞的寄生虫入侵是通过将寄生虫直接从靶细胞转移到T细胞而发生的,并且对应于T细胞入侵速率的抗原特异性增加。我们的结果提供了对召回反应期间细胞相互作用的深入了解,并提出了病原体破坏免疫反应的机制。

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