Beer Hans-Dietmar, Contassot Emmanuel, French Lars E
Department of Dermatology, Zürich University Hospital, Zürich, Switzerland.
Department of Dermatology, Zürich University Hospital, Zürich, Switzerland.
J Invest Dermatol. 2014 Jul;134(7):1805-1810. doi: 10.1038/jid.2014.76. Epub 2014 Mar 6.
During the past years, significant progress in the understanding of the complexity, regulation, and relevance of innate immune responses underlying several inflammatory conditions with neutrophilic skin involvement has been made. These diseases belong to the novel class of autoinflammatory diseases, and several are caused by mutations in genes regulating the function of innate immune complexes, termed inflammasomes, leading to enhanced secretion of the proinflammatory cytokine IL-1β. Consequently, targeting of IL-1β has proven successful in the treatment of these diseases, and the identification of related pathogenic mechanisms in other more common skin diseases characterized by autoinflammation and neutrophilic tissue damage also provides extended opportunities for therapy by interfering with IL-1 signaling.
在过去几年中,我们对几种伴有嗜中性粒细胞皮肤受累的炎症性疾病所涉及的先天性免疫反应的复杂性、调节机制及相关性的理解取得了重大进展。这些疾病属于新型自身炎症性疾病类别,其中一些是由调节先天性免疫复合物(即炎性小体)功能的基因突变引起的,导致促炎细胞因子IL-1β的分泌增加。因此,靶向IL-1β已被证明在治疗这些疾病方面是成功的,并且在其他以自身炎症和嗜中性粒细胞组织损伤为特征的更常见皮肤病中识别相关致病机制,也为通过干扰IL-1信号传导进行治疗提供了更多机会。