Department of Otolaryngology Head and Neck Surgery Surgery, Sichuan Provincial People's Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, China.
Department of Emergency Medicine, Laboratory of Emergency Medicine, West China Hospital, and Disaster Medical Center, Sichuan University, Chengdu, Sichuan, China.
Front Immunol. 2023 Sep 22;14:1250541. doi: 10.3389/fimmu.2023.1250541. eCollection 2023.
Previously, it was believed that type III interferon (IFN-III) has functions similar to those of type I interferon (IFN-I). However, recently, emerging findings have increasingly indicated the non-redundant role of IFN-III in innate antiviral immune responses. Still, the regulatory activity of IFN-III in adaptive immune response has not been clearly reported yet due to the low expression of IFN-III receptors on most immune cells. In the present study, we reviewed the adjuvant, antiviral, antitumor, and disease-moderating activities of IFN-III in adaptive immunity; moreover, we further elucidated the mechanisms of IFN-III in mediating the adaptive antiviral immune response in a thymic stromal lymphopoietin (TSLP)-dependent manner, a pleiotropic cytokine involved in mucosal adaptive immunity. Research has shown that IFN-III can enhance the antiviral immunogenic response in mouse species by activating germinal center B (GC B) cell responses after stimulating TSLP production by microfold (M) cells, while in human species, TSLP exerts OX40L for regulating GC B cell immune responses, which may also depend on IFN-III. In conclusion, our review highlights the unique role of the IFN-III/TSLP axis in mediating host adaptive immunity, which is mechanically different from IFN-I. Therefore, the IFN-III/TSLP axis may provide novel insights for clinical immunotherapy.
先前,人们认为 III 型干扰素(IFN-III)具有与 I 型干扰素(IFN-I)相似的功能。然而,最近新出现的发现越来越表明 IFN-III 在先天抗病毒免疫反应中具有非冗余的作用。尽管如此,由于大多数免疫细胞上 IFN-III 受体的低表达,IFN-III 在适应性免疫反应中的调节活性尚未得到明确报道。在本研究中,我们回顾了 IFN-III 在适应性免疫中的佐剂、抗病毒、抗肿瘤和疾病调节活性;此外,我们进一步阐明了 IFN-III 通过依赖胸腺基质淋巴细胞生成素(TSLP)的方式介导适应性抗病毒免疫反应的机制,TSLP 是一种参与黏膜适应性免疫的多效细胞因子。研究表明,IFN-III 可以通过刺激微皱褶(M)细胞产生 TSLP 来激活生发中心 B(GC B)细胞反应,从而增强小鼠物种的抗病毒免疫原性反应,而在人类物种中,TSLP 通过调节 GC B 细胞免疫反应发挥 OX40L 的作用,这也可能依赖于 IFN-III。总之,我们的综述强调了 IFN-III/TSLP 轴在介导宿主适应性免疫中的独特作用,其机制与 IFN-I 不同。因此,IFN-III/TSLP 轴可能为临床免疫治疗提供新的见解。