The role of senescent T cells in immunopathology.
The role of senescent T cells in immunopathology.
复制标题
衰老T细胞在免疫病理学中的作用。
DOI:
10.1111/acel.13272
复制
发表时间:
2020-12
期刊:
影响因子:
7.8
通讯作者:
Akbar AN
中科院分区:
文献类型:
--
作者:
Covre LP;De Maeyer RPH;Gomes DCO;Akbar AN
The development of senescence in tissues of different organs and in the immune system are usually investigated independently of each other although during ageing, senescence in both cellular systems develop concurrently. Senescent T cells are highly inflammatory and secrete cytotoxic mediators and express natural killer cells receptors (NKR) that bypass their antigen specificity. Instead they recognize stress ligands that are induced by inflammation or infection of different cell types in tissues. In this article we discuss data on T cell senescence, how it is regulated and evidence for novel functional attributes of senescent T cells. We discuss an interactive loop between senescent T cells and senescent non‐lymphoid cells and conclude that in situations of intense inflammation, senescent cells may damage healthy tissue. While the example for immunopathology induced by senescent cells that we highlight is cutaneous leishmaniasis, this situation of organ damage may apply to other infections, including COVID‐19 and also rheumatoid arthritis, where ageing, inflammation and senescent cells are all part of the same equation. Senescence occurs in tissues as well as in the immune system but the interaction between this is poorly understood. Senescent T cells are pro‐inflammatory, express NK receptors that can act independent of the TCR, and are highly cytotoxic. They recognise stress ligands expressed by cells in inflamed or infected tissues or as a consequence of cellular senescence. Here, we discuss how senescent T cells might contribute to exacerbated tissue damage in infectous contexts by interacting with senescent stromal cells. We focus on cutaneous leishmaniasis as a model for this but suggest that this occurs in other infections such as COVID‐19 and indeed autoimmune diseases such as rheumatoid arthritis.
登录
查看更多内容
影响因子:
64.8
作者:
Baker DJ;Childs BG;Durik M;Wijers ME;Sieben CJ;Zhong J;Saltness RA;Jeganathan KB;Verzosa GC;Pezeshki A;Khazaie K;Miller JD;van Deursen JM
通讯作者:
van Deursen JM
DOI:
10.1146/annurev-pathol-121808-102144
发表时间:
2010
期刊:
Annual review of pathology
影响因子:
--
作者:
Coppé JP;Desprez PY;Krtolica A;Campisi J
通讯作者:
Campisi J
影响因子:
6.5
作者:
Da-Cruz, Alda M.;Oliveira-Neto, Manoel P.;Coutinho, Sergio G.
通讯作者:
Coutinho, Sergio G.
影响因子:
18.2
作者:
Campisi J
通讯作者:
Campisi J
DOI:
10.1084/jem.178.2.427
发表时间:
1993-08-01
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Akbar AN;Borthwick N;Salmon M;Gombert W;Bofill M;Shamsadeen N;Pilling D;Pett S;Grundy JE;Janossy G
通讯作者:
Janossy G