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Protein & Cell ; (12): 322-332, 2018.
Artigo em Inglês | WPRIM | ID: wpr-756970

RESUMO

Immunosuppressive regulatory T lymphocytes (Treg) expressing the transcription factor Foxp3 play a vital role in the maintenance of tolerance of the immune-system to self and innocuous non-self. Most Treg that are critical for the maintenance of tolerance to self, develop as an independent T-cell lineage from common T cell precursors in the thymus. In this organ, their differentiation requires signals from the T cell receptor for antigen, from co-stimulatory molecules, as well as from cytokine-receptors. Here we focus on the cytokines implicated in thymic development of Treg, with a particular emphasis on the roles of interleukin-2 (IL-2) and IL-15. The more recently appreciated involvement of TGF-β in thymic Treg development is also briefly discussed. Finally, we discuss how cytokine-dependence of Treg development allows for temporal, quantitative, and potentially qualitative modulation of this process.


Assuntos
Animais , Camundongos , Diferenciação Celular , Genética , Citocinas , Alergia e Imunologia , Fatores de Transcrição Forkhead , Genética , Alergia e Imunologia , Regulação da Expressão Gênica , Tolerância Imunológica , Genética , Interleucina-15 , Genética , Alergia e Imunologia , Interleucina-2 , Genética , Alergia e Imunologia , Receptores de Antígenos de Linfócitos T , Genética , Alergia e Imunologia , Linfócitos T Reguladores , Alergia e Imunologia , Fator de Crescimento Transformador beta , Genética , Alergia e Imunologia
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