Battaglia Manuela, Stabilini Angela, Tresoldi Eleonora
San Raffaele Telethon Institute for Gene Therapy, Milan, Italy.
Methods Mol Biol. 2012;821:279-93. doi: 10.1007/978-1-61779-430-8_17.
CD4(+)CD25(+)FOXP3(+) T regulatory (Treg) cells are pivotal for the induction and maintenance of peripheral tolerance in both mice and humans. The possibility to use Treg cells for the treatment of T-cell-mediated diseases has recently gained increasing momentum. However, given the limited amount of circulating FOXP3(+) Treg cells, efficient methods for their ex vivo expansion are highly desirable. Rapamycin allows for in vitro expansion of murine and human FOXP3(+) Treg cells, which maintain their regulatory phenotype and suppressive capacity. Here, we describe in detail the powerful methods for enriching human FOXP3(+) Treg cells starting from unfractionated CD4(+) T cells or for expanding CD25(+)-enriched Treg cells in the presence of rapamycin.
CD4(+)CD25(+)FOXP3(+) 调节性T(Treg)细胞对于小鼠和人类外周免疫耐受的诱导和维持至关重要。利用Treg细胞治疗T细胞介导疾病的可能性最近越来越受到关注。然而,鉴于循环中FOXP3(+) Treg细胞数量有限,非常需要有效的体外扩增方法。雷帕霉素能够在体外扩增小鼠和人类FOXP3(+) Treg细胞,这些细胞可维持其调节表型和抑制能力。在此,我们详细描述了从未分选的CD4(+) T细胞开始富集人类FOXP3(+) Treg细胞,或在雷帕霉素存在下扩增富含CD25(+)的Treg细胞的有效方法。