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Please use this identifier to cite or link to this item: http://hdl.handle.net/10451/6051

Título: Identification of regulatory Foxp3+ invariant NKT cells induced by TGF-b
Autor: Monteiro, Marta
Almeida, Catarina F.
Caridade, Marta
Ribot, Julie C.
Duarte, Joana
Agua-Doce, Ana
Wollenberg, Ivonne
Silva-Santos, Bruno
Graça, Luís
Palavras-chave: Foxp3+
Invariant NKT (iNKT) cells
Encephalomyelitis, autoimmune, experimental
Natural killer T-cells
Issue Date: Jul-2010
Editora: American Association of Immunologists
Citação: J Immunol 2010;185;2157-2163
Resumo: Invariant NKT (iNKT) cells were shown to prevent the onset of experimental autoimmune encephalomyelitis in mice following administration of their specific TCR agonist alpha-galactosylceramide. We found that this protection was associated with the emergence of a Foxp3(+) iNKT cell population in cervical lymph nodes. We demonstrate that the differentiation of these cells is critically dependent on TGF-beta in both mice and humans. Moreover, in vivo generation of Foxp3(+) iNKT cells was observed in the TGF-beta-rich environment of the murine gut. Foxp3(+) iNKT cells displayed a phenotype similar to that of Foxp3(+) regulatory T cells, and they suppress through a contact-dependent, glucocorticoid-induced TNFR-mediated mechanism. Nevertheless, Foxp3(+) iNKT cells retain distinctive NKT cell characteristics, such as promyelocytic leukemia zinc finger protein expression and preferential homing to the liver following adoptive transfer, where they stably maintained Foxp3 expression. Our data thus unveil an unexpected capacity of iNKT cells to acquire regulatory functions that may contribute to the establishment of immunological tolerance.
Descrição: ©2010 by The American Association of Immunologists, Inc. All rights reserved.
Arbitragem científica: yes
URI: http://hdl.handle.net/10451/6051
doi:10.4049/jimmunol.1000359
ISSN: 0022-1767
Appears in Collections:IMM - Artigos em Revistas Internacionais

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