| Literature DB >> 27718447 |
S Elizabeth Franks1, Andrew Getahun2, P Mark Hogarth3, John C Cambier4.
Abstract
B cells have emerged as effective targets for therapeutic intervention in autoimmunities in which the ultimate effectors are antibodies, as well as those in which T cells are primary drivers of inflammation. Proof of this principle has come primarily from studies of the efficacy of Rituximab, an anti-CD20 mAb that depletes B cells, in various autoimmune settings. These successes have inspired efforts to develop more effective anti-CD20s tailored for specific needs, as well as biologicals and small molecules that suppress B cell function without the risks inherent in B cell depletion. Here we review the current status of B cell-targeted therapies for autoimmunity. Copyright ÂEntities:
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Year: 2016 PMID: 27718447 PMCID: PMC5127449 DOI: 10.1016/j.coi.2016.09.003
Source DB: PubMed Journal: Curr Opin Immunol ISSN: 0952-7915 Impact factor: 7.486