Minutti Carlos M, Jackson-Jones Lucy H, García-Fojeda Belén, Knipper Johanna A, Sutherland Tara E, Logan Nicola, Ringqvist Emma, Guillamat-Prats Raquel, Ferenbach David A, Artigas Antonio, Stamme Cordula, Chroneos Zissis C, Zaiss Dietmar M, Casals Cristina, Allen Judith E
Department of Biochemistry and Molecular Biology I, Complutense University of Madrid, 28040-Madrid, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Respiratorias (CIBERES), Instituto de Salud Carlos III, 28029-Madrid, Spain.
Science. 2017 Jun 9;356(6342):1076-1080. doi: 10.1126/science.aaj2067. Epub 2017 May 11.
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.
2型免疫反应可控制蠕虫感染并维持组织稳态,但如果调节不当,可能导致过敏和纤维化。我们发现了2型介导的巨噬细胞激活的局部组织特异性增强因子。在肺部,表面活性蛋白A(SP-A)增强了白细胞介素-4(IL-4)依赖性巨噬细胞的增殖和激活,加速了寄生虫清除,并减少了肺部迁移性蠕虫感染后的肺损伤。在腹腔和肝脏中,细菌感染后肝脏修复需要C1q增强2型巨噬细胞激活,但在腹膜透析后会导致纤维化。IL-4驱动这些结构相关的防御胶原蛋白、SP-A和C1q的产生,以及它们的受体肌球蛋白18A的表达。这些发现揭示了不同组织中存在局部2型反应所需的放大系统。