Ruan Pinglang, Wang Susu, Yang Ming, Wu Haijing
Department of Dermatology, Second Xiangya Hospital, Central South University, Hunan Key Laboratory of Medical Epigenomics, Changsha, Hunan Province, China.
Department of Anesthesiology, Second Xiangya Hospital, Central South University, Changsha, Hunan Province, China.
Rheumatol Immunol Res. 2022 Oct 20;3(3):128-135. doi: 10.2478/rir-2022-0021. eCollection 2022 Oct.
Aging-associated immune changes, termed immunosenescence, occur with impaired robust immune responses. This immune response is closely related to a greater risk of development of autoimmune disease (AID), which results in increased levels of autoantibodies and increased morbidity and mortality. In addition, lifestyle-related risk factors play a pivotal role in AID, which may be probable via senescence-related immune cell subsets. Age-associated B cell (ABC) subsets have been observed in those who have rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and multiple sclerosis (MS). Here, this review aims to highlight the mechanisms of ABCs with lifestyle interventions in AID, especially how immunosenescence affects the pathogenesis of AID and the future of aging-associated lifestyle interventions in immunosenescence of AID.
与衰老相关的免疫变化,即免疫衰老,伴随着强大免疫反应受损而发生。这种免疫反应与自身免疫性疾病(AID)发生风险增加密切相关,自身免疫性疾病会导致自身抗体水平升高以及发病率和死亡率增加。此外,与生活方式相关的风险因素在自身免疫性疾病中起关键作用,这可能是通过与衰老相关的免疫细胞亚群实现的。在类风湿性关节炎(RA)、系统性红斑狼疮(SLE)和多发性硬化症(MS)患者中已观察到与年龄相关的B细胞(ABC)亚群。在此,本综述旨在强调生活方式干预在自身免疫性疾病中ABCs的作用机制,特别是免疫衰老如何影响自身免疫性疾病的发病机制以及衰老相关生活方式干预在自身免疫性疾病免疫衰老中的未来发展。