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Intravital mucosal imaging of CD8(+) resident memory T cells shows tissue-autonomous recall responses that amplify secondary memory

机译:CD8(+)驻留存储器T细胞的滚内粘膜成像显示组织自主召回响应,其放大次要记忆

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CD8(+) T cell immunosurveillance dynamics influence the outcome of intracellular infections and cancer. Here we used two-photon intravital microscopy to visualize the responses of CD8(+) resident memory T cells (T-RM cells) within the reproductive tracts of live female mice. We found that mucosal T-RM cells were highly motile, but paused and underwent in situ division after local antigen challenge. T-RM cell reactivation triggered the recruitment of recirculating memory T cells that underwent antigen-independent T-RM cell differentiation in situ. However, the proliferation of pre-existing T-RM cells dominated the local mucosal recall response and contributed most substantially to the boosted secondary T-RM cell population. We observed similar results in skin. Thus, T-RM cells can autonomously regulate the expansion of local immunosurveillance independently of central memory or proliferation in lymphoid tissue.
机译:CD8(+)T细胞免疫检疫动力学影响细胞内感染和癌症的结果。 在这里,我们使用了双光子膀胱椎间体显微镜,以使CD8(+)驻留记忆T细胞(T-RM细胞)在活性雌性小鼠的生殖道内的响应可视化。 我们发现粘膜T-RM细胞是高度动机,但在局部抗原攻击后暂停和在原位分区中进行。 T-RM细胞再激活触发循环核心循环仪T细胞的募集,该细胞经历了抗原独立于抗原T-RM细胞分化。 然而,预先存在的T-RM细胞的增殖主要占据局部粘膜召回响应,并最大限度地促进促进的次生T-RM细胞群。 我们观察到皮肤的类似结果。 因此,T-RM细胞可以自主调节局部记忆或淋巴组织中的中央记忆或增殖的局部免疫抑制的膨胀。

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