Immunosenescence, immunotolerance and rejection: clinical aspects in solid organ transplantation

被引:0
|
作者
Rubino, Graziella [1 ,2 ,3 ]
Yoeruek, Efdal [4 ,5 ]
机构
[1] Univ Hosp Tubingen, Dept Trop Med, Wilhelmstr 27, D-72074 Tubingen, Germany
[2] Univ Ulm, Inst Transfus Med, D-89081 Ulm, Germany
[3] Inst Clin Transfus Med & Immunogenet Ulm, D-89081 Ulm, Germany
[4] Berit Klin, Gastrointestinal Ctr, Florastr 1, CH-9403 Goldach, Switzerland
[5] Univ Hosp Tubingen, Dept Ophthalmol, Elfriede Alhorn Str 7, D-72076 Tubingen, Germany
关键词
Aging; Immunosenescence; T cells; Inflammation; Transplantation; REGULATORY T-CELLS; CONGENITAL CYTOMEGALOVIRUS-INFECTION; SENESCENT SECRETORY PHENOTYPE; CORNEAL ENDOTHELIAL-CELLS; CELLULAR SENESCENCE; PERIPHERAL-BLOOD; TH17; CELLS; TNF-ALPHA; INCREASED EXPRESSION; ALLOGRAFT-REJECTION;
D O I
10.1016/j.trim.2024.102068
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
As a consequence of increased lifespan and rising number of elderly individuals developing end-stage organ disease, the higher demand for organs along with a growing availability for organs from older donors pose new challenges for transplantation. During aging, dynamic adaptations in the functionality and structure of the biological systems occur. Consistently, immunosenescence (IS) accounts for polydysfunctions within the lymphocyte subsets, and the onset of a basal but persistent systemic inflammation characterized by elevated levels of pro-inflammatory mediators. There is an emerging consensus about a causative link between such hallmarks and increased susceptibility to morbidities and mortality, however the role of IS in solid organ transplantation (SOT) remains loosely addressed. Dissecting the immune-architecture of immunologicallyprivileged sites may prompt novel insights to extend allograft survival. A deeper comprehension of IS in SOT might unveil key standpoints for the clinical management of transplanted patients.
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页数:10
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