Gulla Surendra, Reddy Madhava C, Reddy Vajra C, Chitta Sriram, Bhanoori Manjula, Lomada Dakshayani
Department of Biotechnology and Bioinformatics, Yogi Vemana University, Kadapa, Andhra Pradesh, India.
Katuri Medical College and Hospital, Chinnakondrupadu, Guntur, India.
Int Rev Immunol. 2023;42(5):347-363. doi: 10.1080/08830185.2022.2064461. Epub 2022 May 20.
The thymus is a primary lymphoid organ, essential for the development of T-cells that will protect from invading pathogens, immune disorders, and cancer. The thymus decreases in size and cellularity with age referred to as thymus involution or atrophy. This involution causes decreased T-cell development and decreased naive T-cell emigration to the periphery, increased proportion of memory T cells, and a restricted, altered T-cell receptor (TCR) repertoire. The changes in composition and function of the circulating T cell pool as a result of thymic involution led to increased susceptibility to infectious diseases including the recent COVID and a higher risk for autoimmune disorders and cancers. Thymic involution consisting of both structural and functional loss of the thymus has a deleterious effect on T cell development, T cell selection, and tolerance. The mechanisms which act on the structural (cortex and medulla) matrix of the thymus, the gradual accumulation of genetic mutations, and altered gene expressions may lead to immunosenescence as a result of thymus involution. Understanding the molecular mechanisms behind thymic involution is critical for identifying diagnostic biomarkers and targets for treatment help to develop strategies to mitigate thymic involution-associated complications. This review is focused on the consequences of thymic involution in infections, immune disorders, and diseases, identifying potential checkpoints and potential approaches to sustain or restore the function of the thymus particularly in elderly and immune-compromised individuals.
胸腺是一个主要的淋巴器官,对于T细胞的发育至关重要,这些T细胞可抵御入侵的病原体、免疫紊乱和癌症。随着年龄增长,胸腺的大小和细胞数量会减少,这被称为胸腺退化或萎缩。这种退化会导致T细胞发育减少、幼稚T细胞向外周迁移减少、记忆T细胞比例增加以及T细胞受体(TCR)库受限且发生改变。胸腺退化导致循环T细胞库的组成和功能发生变化,从而增加了对包括近期新冠病毒在内的传染病的易感性,以及自身免疫性疾病和癌症的患病风险。胸腺退化包括胸腺的结构和功能丧失,对T细胞发育、T细胞选择和耐受性具有有害影响。作用于胸腺结构(皮质和髓质)基质的机制、基因突变的逐渐积累以及基因表达的改变,可能会因胸腺退化而导致免疫衰老。了解胸腺退化背后的分子机制对于识别诊断生物标志物和治疗靶点至关重要,有助于制定减轻胸腺退化相关并发症的策略。本综述重点关注胸腺退化在感染、免疫紊乱和疾病中的后果,识别潜在的检查点以及维持或恢复胸腺功能的潜在方法,特别是在老年人和免疫功能低下个体中。