Institute of Virology, Medical Center University of Freiburg, Freiburg, Germany.
Spemann Graduate School of Biology and Medicine, Albert Ludwigs University Freiburg, Freiburg, Germany.
Nat Immunol. 2019 May;20(5):593-601. doi: 10.1038/s41590-019-0345-x. Epub 2019 Mar 18.
Interferon-λ (IFN-λ) acts on mucosal epithelial cells and thereby confers direct antiviral protection. In contrast, the role of IFN-λ in adaptive immunity is far less clear. Here, we report that mice deficient in IFN-λ signaling exhibited impaired CD8 T cell and antibody responses after infection with a live-attenuated influenza virus. Virus-induced release of IFN-λ triggered the synthesis of thymic stromal lymphopoietin (TSLP) by M cells in the upper airways that, in turn, stimulated migratory dendritic cells and boosted antigen-dependent germinal center reactions in draining lymph nodes. The IFN-λ-TSLP axis also boosted production of the immunoglobulins IgG1 and IgA after intranasal immunization with influenza virus subunit vaccines and improved survival of mice after challenge with virulent influenza viruses. IFN-λ did not influence the efficacy of vaccines applied by subcutaneous or intraperitoneal routes, indicating that IFN-λ plays a vital role in potentiating adaptive immune responses that initiate at mucosal surfaces.
干扰素-λ(IFN-λ)作用于黏膜上皮细胞,从而提供直接的抗病毒保护。相比之下,IFN-λ 在适应性免疫中的作用还远不清楚。在这里,我们报告说,在感染减毒流感病毒后,缺乏 IFN-λ 信号的小鼠表现出 CD8 T 细胞和抗体反应受损。病毒诱导的 IFN-λ 释放触发了上呼吸道中的 M 细胞合成胸腺基质淋巴细胞生成素(TSLP),反过来又刺激了迁移的树突状细胞,并增强了引流淋巴结中抗原依赖性生发中心反应。IFN-λ-TSLP 轴还增强了流感病毒亚单位疫苗经鼻内免疫后的 IgG1 和 IgA 免疫球蛋白的产生,并提高了小鼠在感染强毒流感病毒后的存活率。IFN-λ 不影响通过皮下或腹腔途径应用的疫苗的功效,表明 IFN-λ 在增强起始于黏膜表面的适应性免疫反应方面发挥着至关重要的作用。