免疫耐受
表型
免疫学
自身免疫
T细胞
调节性T细胞
树突状细胞
移植
细胞
癌症研究
生物
细胞生物学
医学
免疫系统
基因
内科学
白细胞介素2受体
生物化学
遗传学
作者
Martine A. Boks,Judith R. Kager-Groenland,Michiel S.P. Haasjes,Jaap Jan Zwaginga,S. Marieke van Ham,Anja ten Brinke
标识
DOI:10.1016/j.clim.2011.11.011
摘要
Tolerogenic dendritic cells (tDC) are a promising tool for specific cellular therapy to induce immunological tolerance in transplantation and autoimmunity. To date, most described tDC methods have not been converted into clinically applicable protocols and systematic comparison of required functional characteristics, i.e. migration and functional regulatory T cell (Treg) induction, is lacking. We compare clinical-grade tDC generated with vitamin D3, IL-10, dexamethasone, TGFβ or rapamycin. For good migratory capacity and a stable phenotype, additional maturation of tDC was required. Maturation with a cocktail of TNFα, IL-1β and PGE2 induced optimal migration. Importantly, all tDC showed a stable phenotype under pro-inflammatory conditions. Especially IL-10 DC showed most powerful tolerogenic characteristics with high IL-10 production and low T cell activation. Moreover, in a functional suppression assay only IL-10 DC induced Treg that strongly suppressed T cell reactivity. Thus, clinical-grade IL-10 DC show functional characteristics that make them best suited for tolerance-inducing therapies.
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