| Literature DB >> 34756580 |
Christine Braegelmann1, Dennis Niebel1, Joerg Wenzel2.
Abstract
Unlike the established anti-inflammatory drugs with a broad range, new-targeted therapeutic approaches have emerged in the management of autoimmune skin diseases to increase efficacy and decrease adverse reactions on the basis of an improved molecular understanding of pathogenesis. Most inflammatory dermatoses are driven by misled immune responses physiologically directed at exogenous pathogens, that is, type 1 immunity against viral pathogens, type 2 immunity against parasites, and type 3 immunity against fungi and bacteria. Pathogenic hallmarks of these major immune reaction patterns are characterized within this article, and a comprehensive overview of current clinical trials evaluating targeted therapeutics for respective dermatoses is outlined.Entities:
Mesh:
Year: 2021 PMID: 34756580 DOI: 10.1016/j.jid.2021.08.439
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551