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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Naive, Effector, and Memory T Lymphocytes Efficiently Scan Dendritic Cells In Vivo: Contact Frequency in T Cell Zones of Secondary Lymphoid Organs Does Not Depend on LFA-1 Expression and Facilitates Survival of Effector T Cells.
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Naive, Effector, and Memory T Lymphocytes Efficiently Scan Dendritic Cells In Vivo: Contact Frequency in T Cell Zones of Secondary Lymphoid Organs Does Not Depend on LFA-1 Expression and Facilitates Survival of Effector T Cells.

机译:幼稚,效应和记忆T淋巴细胞有效地体内扫描树突状细胞:次要淋巴器官的T细胞区的接触频率不取决于LFA-1表达,并促进了效应T细胞的存活。

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摘要

Contact between T cells and dendritic cells (DCs) is required for their subsequent interaction leading to the induction of adaptive immune responses. Quantitative data regarding the contact frequencies of T cell subsets in different lymphoid organs and species are lacking. Therefore, naive, effector, and memory CD4 T cells were injected into rats in absence of the cognate Ag, and 0.5-96 h later, spleen, lymph nodes, and Peyer's patches were removed. Cryosections were analyzed for contact between donor T cells and endogenous DCs in the T cell zone, and donor cell proliferation. More than 60% of injected naive CD4 T cells were in contact with endogenous DCs at all time points and in all organs analyzed. Surprisingly, we were unable to detect any differences between naive, effector, and memory CD4 T cells despite different expression levels of surface molecules. In addition, contact frequency was similar for T cells in lymphoid organs of rats, mice, and humans; it was unaffected by the absence of LFA-1 (CD11a/CD18), and sustained effector T cells in an activated state. Thus, the architecture of the T cell zone rather than expression patterns of surface molecules determines the contact efficiency between T cells and DCs in vivo.
机译:T细胞与树突状细胞(DC)之间的接触对于它们随后的相互作用(导致诱导适应性免疫反应的诱导)是必需的。缺乏有关不同淋巴器官和物种中T细胞亚群接触频率的定量数据。因此,将天然,效应和记忆的CD4 T细胞注射到不存在同源Ag的大鼠中,并在0.5-96小时后去除脾脏,淋巴结和Peyer斑块。分析冷冻切片的供体T细胞与T细胞区中内源性DC之间的接触,以及供体细胞增殖。在所有时间点和所有被分析的器官中,有超过60%的已注射的原始CD4 T细胞与内源性DC接触。令人惊讶的是,尽管表面分子的表达水平不同,我们仍无法检测到幼稚,效应和记忆CD4 T细胞之间的任何差异。另外,大鼠,小鼠和人类淋巴器官中T细胞的接触频率相似。它不受LFA-1(CD11a / CD18)的缺乏和激活状态的效应T细胞的影响。因此,T细胞区的结构而不是表面分子的表达模式决定了体内T细胞和DC之间的接触效率。

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