IL-10-generated tolerogenic dendritic cells are optimal for functional regulatory T cell induction - A comparative study of human clinical-applicable DC

被引:213
|
作者
Boks, Martine A. [1 ,2 ]
Kager-Groenland, Judith R. [1 ,2 ]
Haasjes, Michiel S. P. [1 ,2 ]
Zwaginga, Jaap Jan [2 ,3 ,4 ]
van Ham, S. Marieke [1 ,2 ]
ten Brinke, Anja [1 ,2 ]
机构
[1] Sanquin Res, Dept Immunopathol, NL-1006 AD Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Landsteiner Lab, NL-1105 AZ Amsterdam, Netherlands
[3] Sanquin Res, Dept Expt Immunohaematol, NL-1006 AD Amsterdam, Netherlands
[4] Leiden Univ, Med Ctr, Dept Immunohaematol & Blood Transfus, Leiden, Netherlands
关键词
Suppression; Regulatory T cells; cGMP; Migration; Stability; Tolerance induction; CARDIAC ALLOGRAFT SURVIVAL; MONOPHOSPHORYL-LIPID-A; UP-REGULATION; IN-VITRO; MATURATION; DIFFERENTIATION; TOLERANCE; LIGANDS; HYPORESPONSIVENESS; CD4(+);
D O I
10.1016/j.clim.2011.11.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
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 D-3, IL-10, dexamethasone, TGF beta, or rapamycin. For good migratory capacity and a stable phenotype, additional maturation of tDC was required. Maturation with a cocktail of TNF alpha, IL-1 beta and PGE(2) induced optimal migration. Importantly, all tDC showed a stable phenotype under proinflammatory 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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:332 / 342
页数:11
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