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Understanding and measuring human B-cell tolerance and its breakdown in autoimmune disease.
Cashman, Kevin S; Jenks, Scott A; Woodruff, Matthew C; Tomar, Deepak; Tipton, Christopher M; Scharer, Christopher D; Eun-Hyung Lee, F; Boss, Jeremy M; Sanz, Iñaki.
Afiliación
  • Cashman KS; Department of Medicine, Division of Rheumatology, Emory University, Atlanta, GA, USA.
  • Jenks SA; Lowance Center for Human Immunology, Emory University, Atlanta, GA, USA.
  • Woodruff MC; Department of Medicine, Division of Rheumatology, Emory University, Atlanta, GA, USA.
  • Tomar D; Lowance Center for Human Immunology, Emory University, Atlanta, GA, USA.
  • Tipton CM; Department of Medicine, Division of Rheumatology, Emory University, Atlanta, GA, USA.
  • Scharer CD; Lowance Center for Human Immunology, Emory University, Atlanta, GA, USA.
  • Eun-Hyung Lee F; Department of Medicine, Division of Rheumatology, Emory University, Atlanta, GA, USA.
  • Boss JM; Lowance Center for Human Immunology, Emory University, Atlanta, GA, USA.
  • Sanz I; Department of Medicine, Division of Rheumatology, Emory University, Atlanta, GA, USA.
Immunol Rev ; 292(1): 76-89, 2019 11.
Article en En | MEDLINE | ID: mdl-31755562
ABSTRACT
The maintenance of immunological tolerance of B lymphocytes is a complex and critical process that must be implemented as to avoid the detrimental development of autoreactivity and possible autoimmunity. Murine models have been invaluable to elucidate many of the key components in B-cell tolerance; however, translation to human homeostatic and pathogenic immune states can be difficult to assess. Functional autoreactive, flow cytometric, and single-cell cloning assays have proven to be critical in deciphering breaks in B-cell tolerance within autoimmunity; however, newer approaches to assess human B-cell tolerance may prove to be vital in the further exploration of underlying tolerance defects. In this review, we supply a comprehensive overview of human immune tolerance checkpoints with associated mechanisms of enforcement, and highlight current and future methodologies which are likely to benefit future studies into the mechanisms that become defective in human autoimmune conditions.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Autoantígenos / Enfermedades Autoinmunes / Linfocitos B / Autoinmunidad / Tolerancia Inmunológica Idioma: En Revista: Immunol Rev Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Autoantígenos / Enfermedades Autoinmunes / Linfocitos B / Autoinmunidad / Tolerancia Inmunológica Idioma: En Revista: Immunol Rev Año: 2019 Tipo del documento: Article