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Cellular targets of regulatory B cell-mediated suppression.
Rosser, Elizabeth C; Blair, Paul A; Mauri, Claudia.
Afiliación
  • Rosser EC; Centre for Rheumatology, Division of Medicine, University College London, 5 University Street, London WC1E 6JF, United Kingdom.
  • Blair PA; Centre for Rheumatology, Division of Medicine, University College London, 5 University Street, London WC1E 6JF, United Kingdom.
  • Mauri C; Centre for Rheumatology, Division of Medicine, University College London, 5 University Street, London WC1E 6JF, United Kingdom. Electronic address: c.mauri@ucl.ac.uk.
Mol Immunol ; 62(2): 296-304, 2014 Dec.
Article en En | MEDLINE | ID: mdl-24556109
Regulatory B cells (Bregs) are defined by their ability to restrain inflammatory responses both in vivo and in vitro. Interleukin 10 (IL-10) production by Bregs is thought to be central to their ability to regulate inflammation, largely due to IL-10s' ability to suppress pro-inflammatory cytokine production by effector lymphocytes and to maintain the differentiation of regulatory T cells (Tregs). However, with an increase in available published data, it has become evident that Bregs utilize a number of suppressive mechanisms in order to alter the activation of a variety of different lymphocytes. Here, we summarize the multiplicity of cellular targets of Breg-mediated suppression and describe the mechanisms employed by Bregs to suppress chronic inflammatory responses.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfocitos B Reguladores / Inmunosupresores Límite: Animals / Humans Idioma: En Revista: Mol Immunol Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfocitos B Reguladores / Inmunosupresores Límite: Animals / Humans Idioma: En Revista: Mol Immunol Año: 2014 Tipo del documento: Article País de afiliación: Reino Unido