Immunosenescence in autoimmune diseases

被引:0
作者
Hu, Huifang [1 ,2 ]
Zhang, Guangyue [1 ,2 ]
Chen, Tao [1 ,2 ]
Liu, Yi [1 ,2 ]
Meng, Liesu [3 ,4 ]
Holmdahl, Rikard [5 ]
Dai, Lunzhi [6 ]
Zhao, Yi [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Rheumatol & Immunol, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Clin Inst Inflammat & Immunol, Frontiers Sci Ctr Dis related Mol Network, Chengdu 610041, Sichuan, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 2, Dept Rheumatol, Xian 710004, Shaanxi, Peoples R China
[4] Xi An Jiao Tong Univ, Affiliated Hosp 2, Natl Joint Engn Res Ctr Biodiagnost & Biotherapy, Xian 710004, Shaanxi, Peoples R China
[5] Karolinska Inst, Dept Med Biochem & Biophys, Div Immunol, Med Inflammat Res, Stockholm, Sweden
[6] Sichuan Univ, West China Hosp, Natl Clin Res Ctr Geriatr, State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Immunosenescence; Aging; Autoimmune diseases; Immune system; Autoimmunity; REGULATORY T-CELLS; RHEUMATOID-ARTHRITIS; B-CELLS; NATURAL AUTOANTIBODIES; PREMATURE SENESCENCE; CROSS-REACT; DNA-DAMAGE; LUPUS; SELECTION; PATHWAYS;
D O I
10.1016/j.autrev.2025.103805
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autoimmune diseases (AIDs) are a group of disorders in which the immune system mistakenly attacks the body's own tissues, characterized by the loss of tolerance to self-antigens and destruction of tissues. Aging is a natural process of physiological decline that also alters the immune system, a condition known as immunosenescence. During immunosenescence, the immune system undergoes various changes, including modifications and antigenicity of self-antigens, abnormalities in the quantity, phenotype, and function of lymphocytes and antibodies, as well as a narrowing of the B and T cell receptor repertoire, changes that may increase susceptibility to AIDs. Additionally, senescent immune cells and the senescence-associated secretory phenotype (SASP) contribute to target organ involvement in AIDs, exacerbating chronic inflammation and tissue damage. Mitochondrial dysfunction and metabolic imbalances in AIDs lead to the accumulation of senescent cells, which act as upstream drivers of immunosenescence. In this review, we summarize the bidirectional relationship between AIDs and immunosenescence, as well as its potential mechanisms. Therapeutic approaches targeting immunosenescence in AIDs remain at an early stage. Strategies aimed at resetting or reversing the aging immune system are expected to become a novel direction in the future.
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页数:13
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