Piccirillo Ciriaco A
Department of Microbiology and Immunology, Center for the Study of Host Resistance, McGill University, Montreal, Quebec, Canada.
Cytokine. 2008 Sep;43(3):395-401. doi: 10.1016/j.cyto.2008.07.469. Epub 2008 Aug 22.
Regulatory T (Treg) cells have emerged as a central control point in the modulation of various immune responses, including autoimmune responses and immunity to transplants, allergens, tumors, and infectious microbes. The immune system has evolved complex processes to ensure tolerance to autoantigens while preserving the potential to mount and maintain life-long humoral and cellular immune responses against invading pathogens. In this review, we summarize research showing that naturally occurring (nTreg) and induced Treg (iTreg) cell subsets, and in particular CD4+Foxp3+ Treg cells, are critical in the control of immune responses in rodents and humans. We also discuss the cellular and molecular factors that affect CD4+Foxp3+ Treg cell development, homeostasis, and function and consequential immunity to self and non-self antigens. Recent studies have shed light in our understanding of the development of novel methods of autoimmune disease prevention and treatment via enhancing and re-establishing Treg-mediated dominant control over self-reactive T cells in animal models and humans.
调节性T(Treg)细胞已成为调节各种免疫反应的核心控制点,包括自身免疫反应以及对移植、过敏原、肿瘤和传染性微生物的免疫反应。免疫系统已进化出复杂的过程,以确保对自身抗原的耐受性,同时保留针对入侵病原体产生并维持终身体液和细胞免疫反应的潜力。在本综述中,我们总结了相关研究,这些研究表明天然存在的(nTreg)和诱导性Treg(iTreg)细胞亚群,特别是CD4+Foxp3+ Treg细胞,在啮齿动物和人类的免疫反应控制中至关重要。我们还讨论了影响CD4+Foxp3+ Treg细胞发育、稳态和功能以及对自身和非自身抗原的后续免疫反应的细胞和分子因素。最近的研究为我们理解通过增强和重新建立Treg介导的对动物模型和人类自身反应性T细胞的主导控制来预防和治疗自身免疫性疾病的新方法提供了启示。