Department of Gastroenterology, Third Xiangya Hospital of Central South University, Changsha, China.
Hunan Key Laboratory of Nonresolving Inflammation and Cancer, Changsha, China.
Mediators Inflamm. 2017;2017:4927964. doi: 10.1155/2017/4927964. Epub 2017 Sep 12.
induces a complicated local and systematic immune response and contributes to the carcinogenesis of gastric cancer. A primary type 1 immune response is evoked by since its occurrence. However, it is not unusual that an inhibitory immunity is dominant in -associated diseases, which are promoted by the formation of immunosuppressive microenvironment. But whether group 2 innate lymphoid cells (ILC2s) plays a critical role in -induced skewed type 2 immunity is still unclear. In the present study, firstly, we confirmed that type 1 immunity was inhibited and type 2 immunity were undisturbed or promoted after infection in vitro and in vivo. Secondly, GATA-3 was firstly found to be increased in the interstitial lymphocytes from -associated gastric cancer, among them, Lin-GATA-3 cells and LinGATA-3 cells were also found to be enhanced, which indicated an important role for ILC2s in infection. More importantly, ILC2s were found to be increased after infection in clinical patients and animal models. In conclusion, our results indicated that ILC2-mediated innate immune response might play a potential role in dominant type 2 phenotype and immunosuppressive microenvironment in infection.
诱导复杂的局部和系统性免疫反应,并有助于胃癌的发生。由于其发生,会引发原发性 1 型免疫反应。然而,在与 相关的疾病中,抑制性免疫占优势并不罕见,这是由免疫抑制微环境的形成所促进的。但是,2 型固有淋巴细胞(ILC2)是否在 诱导的偏倚 2 型免疫中起关键作用尚不清楚。在本研究中,首先,我们证实了 感染后体外和体内的 1 型免疫被抑制,而 2 型免疫不受干扰或被促进。其次,首次发现 GATA-3 在与 相关的胃癌间质淋巴细胞中增加,其中 Lin-GATA-3 细胞和 Lin-GATA-3 细胞也被发现增强,这表明 ILC2 在 感染中起重要作用。更重要的是,在临床患者和动物模型中发现感染后 ILC2 增加。总之,我们的结果表明,ILC2 介导的固有免疫反应可能在 感染中主导 2 型表型和免疫抑制微环境中发挥潜在作用。