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从小鼠天然T细胞体外生成CD4+ CD25+调节性细胞。

In vitro generation of CD4+ CD25+ regulatory cells from murine naive T cells.

作者信息

Fantini Massimo C, Dominitzki Sabine, Rizzo Angelo, Neurath Markus F, Becker Christoph

机构信息

Division of Gastroenterology, University of Rome Tor Vergata, Via Montpellier 1, 00133, Rome, Italy.

出版信息

Nat Protoc. 2007;2(7):1789-94. doi: 10.1038/nprot.2007.258.

Abstract

CD4+ CD25+ regulatory T cells (Tregs) are crucial for the maintenance of immunological tolerance. Recent data indicate that Tregs not only develop in the thymus during ontogeny but can also differentiate from naive T cells in the periphery. The following protocol describes a method by which Tregs are generated in vitro by stimulation of naive T cells in the presence of transforming growth factor beta (Ti-Tregs). In vitro-induced regulatory T cells express markers of conventional Treg such as CD25 and the genetic program committing transcription factor FoxP3. Functionally the in vitro-generated Ti-Tregs suppress T-cell activation and proliferation while in vivo these cells have been proven to control inflammation in different animal models, suggesting a potential use of these cells for immunotherapy. The protocol can be completed within 5 days.

摘要

CD4+ CD25+ 调节性T细胞(Tregs)对于维持免疫耐受至关重要。最近的数据表明,Tregs不仅在个体发育过程中于胸腺中发育,还可在外周从初始T细胞分化而来。以下方案描述了一种在转化生长因子β存在的情况下通过刺激初始T细胞在体外生成Tregs的方法(Ti-Tregs)。体外诱导的调节性T细胞表达常规Treg的标志物,如CD25以及决定转录因子FoxP3的遗传程序。在功能上,体外生成的Ti-Tregs抑制T细胞活化和增殖,而在体内,这些细胞已被证明可在不同动物模型中控制炎症,这表明这些细胞在免疫治疗方面具有潜在用途。该方案可在5天内完成。

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