| Literature DB >> 31755562 |
Kevin S Cashman1,2, Scott A Jenks1,2, Matthew C Woodruff1,2, Deepak Tomar1,2, Christopher M Tipton1,2, Christopher D Scharer3, F Eun-Hyung Lee2,4, Jeremy M Boss3, Iñaki Sanz1,2.
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.Entities:
Keywords: B-cell; autoreactivity; checkpoint; epigenetics; human; repertoire; tolerance
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Year: 2019 PMID: 31755562 PMCID: PMC6935423 DOI: 10.1111/imr.12820
Source DB: PubMed Journal: Immunol Rev ISSN: 0105-2896 Impact factor: 12.988