Department of Medicine, Rutgers - New Jersey Medical School, Newark, NJ, USA.
Center for Immunity and Inflammation, Rutgers - New Jersey Medical School, Newark, NJ, USA.
Nat Mater. 2019 Mar;18(3):289-297. doi: 10.1038/s41563-018-0271-6. Epub 2019 Jan 21.
Initiation of the innate sterile inflammatory response that can develop in response to microparticle exposure is little understood. Here, we report that a potent type 2 immune response associated with the accumulation of neutrophils, eosinophils and alternatively activated (M2) macrophages was observed in response to sterile microparticles similar in size to wear debris associated with prosthetic implants. Although elevations in interleukin-33 (IL-33) and type 2 cytokines occurred independently of caspase-1 inflammasome signalling, the response was dependent on Bruton's tyrosine kinase (BTK). IL-33 was produced by macrophages and BTK-dependent expression of IL-33 by macrophages was sufficient to initiate the type 2 response. Analysis of inflammation in patient periprosthetic tissue also revealed type 2 responses under aseptic conditions in patients undergoing revision surgery. These findings indicate that microparticle-induced sterile inflammation is initiated by macrophages activated to produce IL-33. They further suggest that both BTK and IL-33 may provide therapeutic targets for wear debris-induced periprosthetic inflammation.
对微粒暴露引发的固有无菌性炎症反应的启动机制还知之甚少。在这里,我们报告了一种强烈的 2 型免疫反应,与假体植入物相关的磨损碎片大小相似的无菌微粒会引发该反应,其特征是中性粒细胞、嗜酸性粒细胞和选择性激活的(M2)巨噬细胞的积累。尽管白细胞介素-33 (IL-33) 和 2 型细胞因子的升高与半胱天冬酶-1 炎性小体信号的发生无关,但该反应依赖于布鲁顿酪氨酸激酶 (BTK)。IL-33 由巨噬细胞产生,巨噬细胞中 BTK 依赖性的 IL-33 表达足以引发 2 型反应。对无菌条件下接受翻修手术的患者的假体周围组织炎症的分析也显示出 2 型反应。这些发现表明,微粒诱导的无菌性炎症是由被激活以产生 IL-33 的巨噬细胞引发的。它们进一步表明,BTK 和 IL-33 都可能成为与磨损碎片相关的假体周围炎症的治疗靶点。