| Literature DB >> 34215369 |
Jacqueline L Paredes1, Ruth Fernandez-Ruiz2, Timothy B Niewold3.
Abstract
T-cell dysregulation has been implicated in the loss of tolerance and overactivation of B cells in systemic lupus erythematosus (SLE). Recent studies have identified T-cell subsets and genetic, epigenetic, and environmental factors that contribute to pathogenic T-cell differentiation, as well as disease pathogenesis and clinical phenotypes in SLE. Many therapeutics targeting T-cell pathways are under development, and although many have not progressed in clinical trials, the recent approval of the calcineurin inhibitor voclosporin is encouraging. Further study of T-cell subsets and biomarkers of T-cell action may pave the way for specific targeting of pathogenic T-cell populations in SLE.Entities:
Keywords: Cytokines; Epigenetics; Lupus; Metabolism; Systemic lupus erythematosus; T cells; T-cell subsets
Mesh:
Year: 2021 PMID: 34215369 PMCID: PMC8262037 DOI: 10.1016/j.rdc.2021.04.005
Source DB: PubMed Journal: Rheum Dis Clin North Am ISSN: 0889-857X Impact factor: 2.032