[Activation-induced cytidine deaminase (AID) involved in the regulation of B cell immune senescence].

Jiaping Xiao, Jun Li, Xinsheng Yao
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Abstract

The humoral immune response of B cells is the key to the protection of specific immunity, and immune aging reshapes its production and function. The decreased B cell immune function is an indicator of immune senescence. The impaired humoral immune function mediated by antibody secreted by B cells leads to a decline in the response of elderly individuals to the vaccine. These people are therefore more susceptible to infection and deterioration, and have a higher incidence of tumors and metabolic diseases. Activation-induced cytidine deaminase (AID) is an enzyme that triggers immunoglobulin class conversion recombination (CSR) and somatic high frequency mutation (SHM). It decreases during immune senescence and is considered to be a biomarker of decreased B cell function in aging mice and humans. Understanding the inherent defects of B-cell immune senescence and the regulation mechanism of AID in the aging process can provide new research ideas for the susceptibility, prevention and treatment of diseases in the elderly.

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激活诱导胞苷脱氨酶(AID)参与B细胞免疫衰老的调控。
B细胞的体液免疫反应是保护特异性免疫的关键,免疫老化重塑了其产生和功能。B细胞免疫功能下降是免疫衰老的标志。由B细胞分泌的抗体介导的体液免疫功能受损导致老年人对疫苗的应答下降。因此,这些人更容易感染和恶化,肿瘤和代谢性疾病的发病率也更高。激活诱导胞苷脱氨酶(Activation-induced cytidine deaminase, AID)是一种触发免疫球蛋白类转化重组(CSR)和体细胞高频突变(SHM)的酶。它在免疫衰老过程中减少,被认为是衰老小鼠和人类B细胞功能下降的生物标志物。了解b细胞免疫衰老的内在缺陷及AID在衰老过程中的调控机制,可为老年疾病的易感性、防治提供新的研究思路。
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