Division of Clinical Research, Medical Mycology Research Center, Chiba University, Chiba, Japan.
Department of Fungal Infection, National Institute of Infectious Diseases, Tokyo, Japan.
PLoS Pathog. 2024 Jan 3;20(1):e1011878. doi: 10.1371/journal.ppat.1011878. eCollection 2024 Jan.
Although chitin in fungal cell walls is associated with allergic airway inflammation, the precise mechanism underlying this association has yet to be elucidated. Here, we investigated the involvement of fungal chitin-binding protein and chitin in allergic airway inflammation. Recombinant Aspergillus fumigatus LdpA (rLdpA) expressed in Pichia pastoris was shown to be an O-linked glycoprotein containing terminal α-mannose residues recognized by the host C-type lectin receptor, Dectin-2. Chitin particles were shown to induce acute neutrophilic airway inflammation mediated release of interleukin-1α (IL-1α) associated with cell death. Furthermore, rLdpA-Dectin-2 interaction was shown to promote phagocytosis of rLdpA-chitin complex and activation of mouse bone marrow-derived dendritic cells (BMDCs). Moreover, we showed that rLdpA potently induced T helper 2 (Th2)-driven allergic airway inflammation synergistically with chitin, and Dectin-2 deficiency attenuated the rLdpA-chitin complex-induced immune response in vivo. In addition, we showed that serum LdpA-specific immunoglobulin levels were elevated in patients with pulmonary aspergillosis.
尽管真菌细胞壁中的几丁质与过敏性气道炎症有关,但这一关联的确切机制尚未阐明。在这里,我们研究了真菌几丁质结合蛋白和几丁质在过敏性气道炎症中的作用。在巴斯德毕赤酵母中表达的重组烟曲霉 LdpA(rLdpA)被证明是一种 O-连接糖蛋白,含有被宿主 C 型凝集素受体 Dectin-2 识别的末端α-甘露糖残基。几丁质颗粒可诱导急性中性粒细胞性气道炎症,介导白细胞介素-1α(IL-1α)的释放与细胞死亡相关。此外,rLdpA-Dectin-2 相互作用可促进 rLdpA-几丁质复合物的吞噬作用和小鼠骨髓来源树突状细胞(BMDCs)的激活。此外,我们发现 rLdpA 与几丁质协同强烈诱导 T 辅助 2(Th2)驱动的过敏性气道炎症,而 Dectin-2 缺乏可减轻体内 rLdpA-几丁质复合物诱导的免疫反应。此外,我们还发现,患有肺部曲霉菌病的患者血清中 LdpA 特异性免疫球蛋白水平升高。