TY - JOUR
T1 - Targeting B cells to treat systemic lupus erythematosus
AU - Tieng, Arlene T.
AU - Zandman-Goddard, Gisele
AU - Peeva, Elena
PY - 2010/12
Y1 - 2010/12
N2 - B cells play a central role in the pathogenesis of systemic lupus erythematosus. Of late, there has been growing interest in utilizing B cells as targets for the development of new treatments for this frequently devastating disease. In addition to producing (auto)antibodies, B cells are involved in a variety of autoantibody-independent pathogenic mechanisms, such as effector functions, cytokine production and costimulation. Therefore, depleting B cells or inhibiting their actions can suppress the immune hyperactivity that is characteristic of systemic lupus erythematosus. This article examines the latest advances in novel B-cell-directed therapies for patients with systemic lupus erythematosus.
AB - B cells play a central role in the pathogenesis of systemic lupus erythematosus. Of late, there has been growing interest in utilizing B cells as targets for the development of new treatments for this frequently devastating disease. In addition to producing (auto)antibodies, B cells are involved in a variety of autoantibody-independent pathogenic mechanisms, such as effector functions, cytokine production and costimulation. Therefore, depleting B cells or inhibiting their actions can suppress the immune hyperactivity that is characteristic of systemic lupus erythematosus. This article examines the latest advances in novel B-cell-directed therapies for patients with systemic lupus erythematosus.
KW - B-cell depletion
KW - B-cell-directed therapies
KW - B-lymphocyte stimulator
KW - CD20
KW - CD22
KW - costimulation
KW - systemic lupus erythematosus
UR - http://www.scopus.com/inward/record.url?scp=78649651762&partnerID=8YFLogxK
U2 - 10.2217/ijr.10.95
DO - 10.2217/ijr.10.95
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AN - SCOPUS:78649651762
SN - 1758-4272
VL - 5
SP - 627
EP - 636
JO - International Journal of Clinical Rheumatology
JF - International Journal of Clinical Rheumatology
IS - 6
ER -