TY - JOUR
T1 - Targeting B cells in treatment of autoimmunity
AU - Franks, S. Elizabeth
AU - Getahun, Andrew
AU - Hogarth, P. Mark
AU - Cambier, John C
PY - 2016/12/1
Y1 - 2016/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84990869246&partnerID=8YFLogxK
U2 - 10.1016/j.coi.2016.09.003
DO - 10.1016/j.coi.2016.09.003
M3 - Review Article
AN - SCOPUS:84990869246
SN - 0952-7915
VL - 43
SP - 39
EP - 45
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
ER -