IFN-α: A key therapeutic target for multiple autoimmune rheumatic diseases
- PMID: 34224903
- DOI: 10.1016/j.drudis.2021.06.010
IFN-α: A key therapeutic target for multiple autoimmune rheumatic diseases
Abstract
Interferon (IFN)-α has emerged as a major therapeutic target for several autoimmune rheumatic diseases. In this review, we focus on clinical and preclinical advances in anti-IFN-α treatments in systemic lupus erythematosus (SLE), primary Sjögren syndrome (pSS), systemic sclerosis (SSc), and dermatomyositis (DM), for which a high medical need persists. Promising achievements were obtained following direct IFN-α neutralization, targeting its production through the cytosolic nucleic acid sensor pathways or by blocking its downstream effects through the type I IFN receptor. We further focus on molecular profiling and data integration approaches as crucial steps to select patients most likely to benefit from anti-IFN-α therapies within a precision medicine approach.
Keywords: Autoimmune rheumatic diseases; Dermatomyositis; Interferon gene signature; Interferon-alpha; Precision medicine; Primary Sjögren syndrome; Systemic lupus erythematosus; Systemic sclerosis; Therapy; Treatment.
Copyright © 2021 Elsevier Ltd. All rights reserved.
Conflict of interest statement
Declaration of Competing Interest All authors are employees of Servier, a company that develops S95021 and holds rights on the 8H1 and 12H5 mAbs used in the SIMOA IFN-α assay.
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