| Literature DB >> 25801878 |
D Comte1, M P Karampetsou2, G C Tsokos2.
Abstract
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease characterized by a loss of tolerance to multiple endogenous antigens. SLE etiology remains largely unknown, despite recent insight into the immunopathogenesis of the disease. T cells are important in the development of the disease by amplifying the immune response and contributing to organ damage. Aberrant signaling, cytokine secretion, and tissue homing displayed by SLE T cells have been extensively studied and the underlying pathogenic molecular mechanisms are starting to be elucidated. T-cell-targeted treatments are being explored in SLE patients. This review is an update on the T-cell abnormalities and related therapeutic options in SLE.Entities:
Keywords: Systemic lupus erythematosus; T cells; epigenetics; interleukin-2 (IL-2); treatment
Mesh:
Substances:
Year: 2015 PMID: 25801878 PMCID: PMC4372812 DOI: 10.1177/0961203314556139
Source DB: PubMed Journal: Lupus ISSN: 0961-2033 Impact factor: 2.911