| Literature DB >> 28495878 |
Carlos M Minutti1,2,3, Lucy H Jackson-Jones3, Belén García-Fojeda1,2, Johanna A Knipper3, Tara E Sutherland3,4, Nicola Logan3, Emma Ringqvist3, Raquel Guillamat-Prats2,5, David A Ferenbach3, Antonio Artigas2,5, Cordula Stamme6, Zissis C Chroneos7, Dietmar M Zaiss3, Cristina Casals1,2, Judith E Allen3,8.
Abstract
The type 2 immune response controls helminth infection and maintains tissue homeostasis but can lead to allergy and fibrosis if not adequately regulated. We have discovered local tissue-specific amplifiers of type 2-mediated macrophage activation. In the lung, surfactant protein A (SP-A) enhanced interleukin-4 (IL-4)-dependent macrophage proliferation and activation, accelerating parasite clearance and reducing pulmonary injury after infection with a lung-migrating helminth. In the peritoneal cavity and liver, C1q enhancement of type 2 macrophage activation was required for liver repair after bacterial infection, but resulted in fibrosis after peritoneal dialysis. IL-4 drives production of these structurally related defense collagens, SP-A and C1q, and the expression of their receptor, myosin 18A. These findings reveal the existence within different tissues of an amplification system needed for local type 2 responses.Entities:
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Year: 2017 PMID: 28495878 PMCID: PMC5737834 DOI: 10.1126/science.aaj2067
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728