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Postthymic maturation influences the CD8 T cell response to antigen

机译:胸腺后成熟影响CD8 T细胞对抗原的反应

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Complete T cell development requires postthymic maturation, and we investigated the influence of this ontological period on the CD8 T cell response to infection by comparing responses of mature CD8 T cells with those of recent thymic emigrants (RTEs). When activated with a noninflammatory stimulus or a bacterial or viral pathogen, CD8 RTEs generated a lower proportion of cytokine-producing effector cells and long-lived memory precursors compared with their mature counterparts. Although peripheral T cell maturation is complete within several weeks after thymic egress, RTE-derived memory cells continued to express inappropriate levels of memory cell markers and display an altered pattern of cytokine production, even 8 weeks after infection. When rechal-lenged, RTE-derived memory cells generated secondary effector cells that were phenotypically and functionally equivalent to those generated by their mature counterparts. The defects at the effector and memory stages were not associated with differences in the expression of T cell receptor-, costimulation-, or activation-associated cell surface markers yet were associated with lower Ly6C expression levels at the effector stage. This work demonstrates that the stage of postthymic maturation influences cell fate decisions and cytokine profiles of stimulated CD8 T cells, with repercussions that are apparent long after cells have progressed from the RTE compartment.
机译:完整的T细胞发育需要胸腺后成熟,并且我们通过比较成熟的CD8 T细胞和最近的胸腺移出物(RTE)的应答,研究了这一本体论时期对CD8 T细胞对感染应答的影响。当用非炎性刺激物或细菌或病毒病原体激活时,与成熟的对应物相比,CD8 RTE产生的细胞因子效应细胞和长寿命记忆前体的比例更低。尽管胸腺外出后数周内外周T细胞成熟完全,但RTE衍生的记忆细胞甚至在感染后8周仍继续表达不适当水平的记忆细胞标志物并显示出细胞因子产生的模式改变。当再呼气时,RTE衍生的记忆细胞产生的次级效应细胞在表型和功能上均等同于它们的成熟对应物。效应子和记忆阶段的缺陷与T细胞受体,共刺激或激活相关的细胞表面标志物表达的差异无关,但与效应子阶段较低的Ly6C表达水平有关。这项工作表明,胸腺后成熟阶段会影响受刺激的CD8 T细胞的细胞命运决定和细胞因子谱,其影响在细胞从RTE隔室发育很长时间后就很明显。

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