cAMP responsive element modulator α promotes effector T cells in systemic autoimmune diseases
- PMID: 37435993
- DOI: 10.1111/imm.13680
cAMP responsive element modulator α promotes effector T cells in systemic autoimmune diseases
Abstract
T lymphocytes play a crucial role in adaptive immunity. Dysregulation of T cell-derived inflammatory cytokine expression and loss of self-tolerance promote inflammation and tissue damage in several autoimmune/inflammatory diseases, including systemic lupus erythematosus (SLE) and psoriasis. The transcription factor cAMP responsive element modulator α (CREMα) plays a key role in the regulation of T cell homeostasis. Increased expression of CREMα is a hallmark of the T cell-mediated inflammatory diseases SLE and psoriasis. Notably, CREMα regulates the expression of effector molecules through trans-regulation and/or the co-recruitment of epigenetic modifiers, including DNA methyltransferases (DNMT3a), histone-methyltransferases (G9a) and histone acetyltransferases (p300). Thus, CREMα may be used as a biomarker for disease activity and/or target for future targeted therapeutic interventions.
Keywords: CREM; epigenetics; lymphocyte; psoriasis; psoriatic arthritis; systemic lupus erythematosus.
© 2023 The Authors. Immunology published by John Wiley & Sons Ltd.
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