FOXP3型
免疫学
免疫系统
白细胞介素2受体
免疫耐受
细胞毒性T细胞
生物
调节性T细胞
CTLA-4号机组
免疫
T细胞
遗传学
体外
标识
DOI:10.1093/intimm/dxq212
摘要
Naturally arising CD25+CD4+ regulatory T cells (Tregs), which specifically express the transcription factor Foxp3, are engaged in the maintenance of immunological self-tolerance and immune homeostasis. They suppress aberrant or excessive immune responses, such as autoimmune disease and allergy. They are also exploited to enhance tumor immunity or establish transplantation tolerance. Foxp3 controls key functional features of Tregs: its expression is sufficient to confer suppressive activity to naive T cells, repress production of cytokines such as interleukin-2 (IL-2) and interferon-gamma (IFN-γ), and up-regulate Treg-associated molecules such as CD25, and cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4). Our current understanding will be discussed on how Foxp3+ Tregs are generated, how they exert suppression, and how they can be exploited at the molecular level to control immune responses in a variety of clinical settings.
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