Goswami Tapas Kumar, Singh Mithilesh, Dhawan Manish, Mitra Saikat, Emran Talha Bin, Rabaan Ali A, Mutair Abbas Al, Alawi Zainab Al, Alhumaid Saad, Dhama Kuldeep
Immunology Section, ICAR-Indian Veterinary Research Institute, Bareilly, India.
Department of Microbiology, Punjab Agricultural University, Ludhiana, India.
Hum Vaccin Immunother. 2022 Dec 31;18(1):2035117. doi: 10.1080/21645515.2022.2035117. Epub 2022 Mar 3.
Autoimmune diseases are caused when immune cells act against self-protein. This biological self-non-self-discrimination phenomenon is controlled by a distinct group of lymphocytes known as regulatory T cells (Tregs), which are key inflammatory response regulators and play a pivotal role in immune tolerance and homeostasis. Treg-mediated robust immunosuppression provides self-tolerance and protection against autoimmune diseases. However, once this system fails to operate or poorly operate, it leads to an extreme situation where immune system reacts against self-antigens and destroys host organs, thus causing autoimmune diseases. Tregs can target both innate and adaptive immunity via modulating multiple immune cells such as neutrophils, monocytes, antigen-presenting cells, B cells, and T cells. This review highlights the Treg-mediated immunosuppression, role of several markers and their interplay during Treg development and differentiation, and advances in therapeutic aspects of Treg cells to reduce severity of autoimmunity-related conditions along with emphasizing limitations and challenges of their usages.
自身免疫性疾病是由免疫细胞攻击自身蛋白质引起的。这种生物性的自我与非自我识别现象由一组独特的淋巴细胞控制,即调节性T细胞(Tregs),它们是关键的炎症反应调节因子,在免疫耐受和体内平衡中起关键作用。Treg介导的强大免疫抑制作用提供了自身耐受性,并预防自身免疫性疾病。然而,一旦这个系统无法运作或运作不佳,就会导致免疫系统对自身抗原产生反应并破坏宿主器官的极端情况,从而引发自身免疫性疾病。Tregs可以通过调节多种免疫细胞,如中性粒细胞、单核细胞、抗原呈递细胞、B细胞和T细胞,来靶向先天免疫和适应性免疫。本综述重点介绍了Treg介导的免疫抑制作用、几种标志物在Treg发育和分化过程中的作用及其相互作用,以及Treg细胞在治疗方面的进展,以降低自身免疫相关病症的严重程度,同时强调了其使用的局限性和挑战。