D'Arena Giovanni, Rossi Giovanni, Vannata Barbara, Deaglio Silvia, Mansueto Giovanna, D'Auria Fiorella, Statuto Teodora, Simeon Vittorio, De Martino Laura, Marandino Aurelio, Del Poeta8 Giovanni, De Feo Vincenzo, Musto Pellegrino
Department of Onco-Hematology, IRCCS "Centro di Riferimento Oncologico della Basilicata", Rionero in Vulture, Italy.
Mediterr J Hematol Infect Dis. 2012;4(1):e2012053. doi: 10.4084/MJHID.2012.053. Epub 2012 Aug 9.
Regulatory T-cells (Tregs) constitute a small subset of cells that are actively involved in maintaining self-tolerance, in immune homeostasis and in antitumor immunity. They are thought to play a significant role in the progression of cancer and are generally increased in patient with chronic lymphocytic leukemia (CLL). Their number correlates with more aggressive disease status and is predictive of the time to treatment, as well. Moreover, it is now clear that dysregulation in Tregs cell frequency and/or function may result in a plethora of autoimmune diseases, including multiple sclerosis, type 1 diabetes mellitus, myasthenia gravis, systemic lupus erythematosus, autoimmune lymphoproliferative disorders, rheumatoid arthritis, and psoriasis. Efforts are made aiming to develop approaches to deplete Tregs or inhibit their function in cancer and autoimmune disorders, as well.
调节性T细胞(Tregs)是一小部分积极参与维持自身耐受性、免疫稳态和抗肿瘤免疫的细胞。它们被认为在癌症进展中起重要作用,并且在慢性淋巴细胞白血病(CLL)患者中通常会增加。它们的数量与更具侵袭性的疾病状态相关,并且也可预测治疗时间。此外,现在很清楚,Tregs细胞频率和/或功能的失调可能导致多种自身免疫性疾病,包括多发性硬化症、1型糖尿病、重症肌无力、系统性红斑狼疮、自身免疫性淋巴增殖性疾病、类风湿性关节炎和银屑病。人们也在努力开发在癌症和自身免疫性疾病中耗尽Tregs或抑制其功能的方法。