| Literature DB >> 31986085 |
Stuart A Cook1,2,3,4, Sebastian Schafer1,2.
Abstract
Interleukin (IL)-11 is upregulated in a wide variety of fibro-inflammatory diseases such as systemic sclerosis, rheumatoid arthritis, pulmonary fibrosis, inflammatory bowel disease, kidney disease, drug-induced liver injury, and nonalcoholic steatohepatitis. IL-11 is a member of the IL-6 cytokine family and has several distinct properties that define its unique and nonredundant roles in disease. The IL-11 receptor is highly expressed on stromal, epithelial and polarized cells, where noncanonical IL-11 signaling drives the three pathologies common to all fibro-inflammatory diseases-myofibroblast activation, parenchymal cell dysfunction, and inflammation-while also inhibiting tissue regeneration. This cytokine has been little studied, and publications on IL-11 peaked in the early 1990s, when it was largely misunderstood. Here we describe recent advances in our understanding of IL-11 biology, outline how misconceptions as to its function came about, and highlight the large potential of therapies targeting IL-11 signaling for treating human disease.Entities:
Keywords: IL-11; IL11; drug target; fibroblast; fibrosis; inflammation; interleukin-11; stroma
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Year: 2020 PMID: 31986085 DOI: 10.1146/annurev-med-041818-011649
Source DB: PubMed Journal: Annu Rev Med ISSN: 0066-4219 Impact factor: 13.739