首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Cognate CD4 help is essential for the reactivation and expansion of CD8 memory T cells directed against the hematopoietic cell-specific dominant minor histocompatibility antigen, H60.
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Cognate CD4 help is essential for the reactivation and expansion of CD8 memory T cells directed against the hematopoietic cell-specific dominant minor histocompatibility antigen, H60.

机译:相关的CD4帮助对于针对造血细胞特异性显性次要组织相容性抗原H60的CD8记忆T细胞的激活和扩增至关重要。

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摘要

In contrast to previous notions of the help-independency of memory CD8 T cells during secondary expansion, here we show that CD4 help is indispensable for the re-expansion of once-helped memory CD8 T cells, using a hematopoietic cell-specific dominant minor histocompatibility (H) antigen, H60, as a model antigen. H60-specific memory CD8 T cells generated during a helped primary response vigorously expanded only when rechallenged under helped conditions. The help requirement for an optimal secondary response was confirmed by a reduction in peak size by CD4 depletion, and was reproduced after skin transplantation. Helpless conditions or noncognate separate help during the secondary response resulted in a significant reduction in the peak size and different response kinetics. Providing CD4 help again during a tertiary challenge restored robust memory expansion; however, the repeated deprivation of help further reduced clonal expansion. Adoptively transferred memory CD8 T cells did not proliferate in CD40L(-/-) hosts. In the CD40(-/-) hosts, marginal memory expansion was detected after priming with male H60 cells but was completely abolished by priming with peptide-loaded CD40(-/-) cells, suggesting the essential role of CD40 and CD40L in memory responses. These results provide insight into the control of minor H antigen-specific CD8 T-cell responses, to maximize the graft-versus-leukemia response.
机译:与先前的记忆CD8 T细胞在辅助扩增过程中的帮助独立性概念相反,这里我们显示,使用造血细胞特异性的显性次要组织相容性,曾经帮助过的记忆CD8 T细胞的再扩增中,CD4帮助是必不可少的。 (H)抗原,H60,作为模型抗原。仅在辅助条件下受到挑战时,在辅助主要反应期间产生的H60特异性记忆CD8 T细胞才会急剧扩增。 CD4耗竭减少了峰的大小,证实了最佳次要反应的帮助要求,并在皮肤移植后得以再现。在次级响应过程中,由于无助的条件或非同源的单独帮助,导致了峰大小的明显减小和不同的响应动力学。在第三次挑战中再次提供CD4帮助可以恢复强大的内存扩展;但是,一再剥夺帮助进一步减少了克隆扩增。过继转移的记忆CD8 T细胞在CD40L(-/-)宿主中不增殖。在CD40(-/-)宿主中,雄性H60细胞启动后检测到边缘记忆扩展,但肽加载的CD40(-/-)细胞启动后完全消除了边缘记忆扩展,提示CD40和CD40L在记忆应答中的重要作用。这些结果提供了对次要H抗原特异性CD8 T细胞反应控制的见解,以最大化移植物抗白血病反应。

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