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Local proliferation maintains a stable pool of tissue-resident memory T cells after antiviral recall responses.
Nature Immunology ( IF 30.5 ) Pub Date : 2018-Feb-01 , DOI: 10.1038/s41590-017-0027-5
Simone L. Park , Ali Zaid , Jyh Liang Hor , Susan N. Christo , Julia E. Prier , Brooke Davies , Yannick O. Alexandre , Julia L. Gregory , Tiffany A. Russell , Thomas Gebhardt , Francis R. Carbone , David C. Tscharke , William R. Heath , Scott N. Mueller , Laura K. Mackay

Although tissue-resident memory T cells (TRM cells) are critical in fighting infection, their fate after local pathogen re-encounter is unknown. Here we found that skin TRM cells engaged virus-infected cells, proliferated in situ in response to local antigen encounter and did not migrate out of the epidermis, where they exclusively reside. As a consequence, secondary TRM cells formed from pre-existing TRM cells, as well as from precursors recruited from the circulation. Newly recruited antigen-specific or bystander TRM cells were generated in the skin without displacement of the pre-existing TRM cell pool. Thus, pre-existing skin TRM cell populations are not displaced after subsequent infections, which enables multiple TRM cell specificities to be stably maintained within the tissue.

中文翻译:

抗病毒召回反应后,局部增殖可维持稳定的组织驻留记忆T细胞库。

尽管组织驻留性记忆T细胞(T RM细胞)在抵抗感染方面至关重要,但在局部病原体再次遭遇后它们的命运尚不清楚。在这里,我们发现皮肤T RM细胞参与了病毒感染的细胞,响应于局部抗原的接触而原位增殖,并且没有迁移出表皮,而表皮只是它们所在的位置。结果,由先前存在的T RM细胞以及从循环中募集的前体形成了次级T RM细胞。在皮肤中产生了新募集的抗原特异性或旁观者T RM细胞,而不会取代现有的T RM细胞池。因此,先前存在的皮肤T RM在随后的感染后,细胞群不会被置换,这使得多种TRM细胞特异性能够在组织内稳定地保持。
更新日期:2018-01-08
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