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Immature dendritic cells suppress collagen-induced arthritis by in vivo expansion of CD49b+ regulatory T cells
被引:84
作者:
Charbonnier, Louis-Marie
van Duivenvoorde, Leonie M.
Apparailly, Florence
Cantos, Celine
Han, Wanda G. H.
Noel, Daniele
Duperray, Christophe
Huizinga, Tom W. J.
Toes, Rene E. M.
Jorgensen, Christian
Louis-Plence, Pascale
机构:
[1] INSERM, U475, F-34197 Montpellier 05, France
[2] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
[3] Ctr Hosp Univ, Hop Lapeyronie, Unite Clin Immunorhumatol Therapeut Malad Articul, Montpellier, France
[4] Univ Montpellier 1, Montpellier, France
关键词:
D O I:
10.4049/jimmunol.177.6.3806
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Dendritic cells (DCs) are specialized APCs with an important role in the initiation and regulation of immune responses. Immature DCs (iDCs) reportedly mediate tolerance in the absence of maturation/inflammatory stimuli, presumably by the induction of regulatory T cells. In this study, we show for the first time that repetitive iDC injections trigger the expansion of a novel regulatory population with high immunomodulatory properties, able to protect mice from collagen-induced arthritis. These regulatory T cells are characterized by the expression of the CD49b molecule and correspond to a CD4(+) alpha-galactosylceramide/CD1d-nonrestricied T cell population producing IL-10. Adoptive transfer of < 10(5) TCR beta(+)CD49b(+) cells isolated from the liver of iDCs-vaccinated mice, conferred a complete protection against arthritis. This protection was associated with an attenuation of the B and T cell response associated with a local secretion of IL-10. Thus, together these data demonstrate that iDCs can expand and activate a novel regulatory population of CD49b(+) T cells, with high immunosuppressive potential able to mediate protection against a systemic autoimmune disease.
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页码:3806 / 3813
页数:8
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