Chatila Talal A
Division of Immunology, Allergy and Rheumatology, Department of Pediatrics, The David Geffen School of Medicine, University of California, Los Angeles, CA 90095-1752, USA.
Endocrinol Metab Clin North Am. 2009 Jun;38(2):265-72, vii. doi: 10.1016/j.ecl.2009.01.002.
CD4 + CD25 + regulatory T (TR) lymphocytes are essential to the maintenance of immunologic tolerance in the host. The discovery of Foxp3 as a transcription factor essential to the differentiation of TR ushered in detailed studies of the molecular mechanisms of TR cell development, peripheral homeostasis, and effector functions. In humans, loss of function mutations in genes that regulate T-cell development and function have been associated with TR cell deficiency or dysfunction and syndromes of autoimmunity and immune dysregulation. Augmentation of TR cells by immunotherapy and pharmacologic agents is a promising strategy for the treatment of allergic and autoimmune diseases.
CD4 + CD25 + 调节性T(TR)淋巴细胞对于维持宿主的免疫耐受至关重要。Foxp3作为TR分化所必需的转录因子的发现,开启了对TR细胞发育、外周稳态和效应功能分子机制的详细研究。在人类中,调节T细胞发育和功能的基因功能丧失突变与TR细胞缺陷或功能障碍以及自身免疫和免疫失调综合征相关。通过免疫疗法和药物增强TR细胞是治疗过敏性和自身免疫性疾病的一种有前景的策略。