Z. Tang, Xianhai Zeng, Juanjuan Li, Hua Zhang, Han-Xing Wu, S. Zhuang, Yiqing Zheng
{"title":"分泌性中耳炎患者Treg/Th17免疫失衡可能与中耳黏膜PI3K/Akt/mTOR信号激活有关","authors":"Z. Tang, Xianhai Zeng, Juanjuan Li, Hua Zhang, Han-Xing Wu, S. Zhuang, Yiqing Zheng","doi":"10.21203/rs.3.rs-94971/v1","DOIUrl":null,"url":null,"abstract":"\n Objective: To assess whether secretory otitis media may be caused by immune imbalance of Treg/Th17 mediated by PI3K/Akt/mTOR signaling, so as to find new therapeutic target.Methods: IL-17, TGF- and IL-6, IL-10 and Th17 cytokines were detected in peripheral blood of OME patients (PC group) and healthy people (NC group) by ELISA. The expression of ROR t mRNA and Foxp3mRNA in PBMC was detected by RT-PCR. OME rat model was established and the changes of lymphocytes in middle ear mucosa and spleen and PI3K/Akt/mTOR signaling in middle ear mucosa were detected by HE staining, IHC, WB and flow cytometry.Results: The immune imbalance of Treg/Th17 in secretory otitis media (OME) was confirmed by the expression of cytokines in OME serum and analysis of ROR T and Foxp3 mRNA which was Th17 and Treg specific transcription respectively. OME rat model further confirmed that Treg/Th17 imbalance could lead to OME as demonstrated by staining of MIDDLE ear mucosa and expression of ROR T and Foxp3. PI3K, Akt, and mTOR proteins were expressed in the MIDDLE ear mucosa of OME group and CON group, respectively. Compared with CON group, the expression of P-MTOR and P-PI3K proteins in the middle ear mucosa of OME group was significantly increased.Conclusions: Treg/Th17 imbalances are found in OME patients and OME animal model and the pathogenic mechanism may be due to systemic abnormal immune response, activated PI3K/Akt/mTOR signaling, abnormal T cell differentiation, leading to middle ear mucosal hyperemia, edema and subsequent occurrence of OME.","PeriodicalId":370947,"journal":{"name":"Clinical Immunology and Immunotherapy","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2020-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"The Immune Imbalance of Treg/Th17 in Otitis Media of Effusion Patients May Be Related to PI3K/Akt/mTOR Signaling Activation in the Middle Ear Mucosa\",\"authors\":\"Z. Tang, Xianhai Zeng, Juanjuan Li, Hua Zhang, Han-Xing Wu, S. Zhuang, Yiqing Zheng\",\"doi\":\"10.21203/rs.3.rs-94971/v1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n Objective: To assess whether secretory otitis media may be caused by immune imbalance of Treg/Th17 mediated by PI3K/Akt/mTOR signaling, so as to find new therapeutic target.Methods: IL-17, TGF- and IL-6, IL-10 and Th17 cytokines were detected in peripheral blood of OME patients (PC group) and healthy people (NC group) by ELISA. The expression of ROR t mRNA and Foxp3mRNA in PBMC was detected by RT-PCR. OME rat model was established and the changes of lymphocytes in middle ear mucosa and spleen and PI3K/Akt/mTOR signaling in middle ear mucosa were detected by HE staining, IHC, WB and flow cytometry.Results: The immune imbalance of Treg/Th17 in secretory otitis media (OME) was confirmed by the expression of cytokines in OME serum and analysis of ROR T and Foxp3 mRNA which was Th17 and Treg specific transcription respectively. OME rat model further confirmed that Treg/Th17 imbalance could lead to OME as demonstrated by staining of MIDDLE ear mucosa and expression of ROR T and Foxp3. PI3K, Akt, and mTOR proteins were expressed in the MIDDLE ear mucosa of OME group and CON group, respectively. Compared with CON group, the expression of P-MTOR and P-PI3K proteins in the middle ear mucosa of OME group was significantly increased.Conclusions: Treg/Th17 imbalances are found in OME patients and OME animal model and the pathogenic mechanism may be due to systemic abnormal immune response, activated PI3K/Akt/mTOR signaling, abnormal T cell differentiation, leading to middle ear mucosal hyperemia, edema and subsequent occurrence of OME.\",\"PeriodicalId\":370947,\"journal\":{\"name\":\"Clinical Immunology and Immunotherapy\",\"volume\":\"19 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-10-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Immunology and Immunotherapy\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21203/rs.3.rs-94971/v1\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Immunology and Immunotherapy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21203/rs.3.rs-94971/v1","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
摘要
目的:探讨分泌性中耳炎是否由PI3K/Akt/mTOR信号介导的Treg/Th17免疫失衡引起,以寻找新的治疗靶点。方法:采用ELISA法检测OME患者(PC组)和正常人(NC组)外周血中IL-17、TGF-、IL-6、IL-10、Th17等细胞因子。RT-PCR检测PBMC中ROR t mRNA和Foxp3mRNA的表达。建立OME大鼠模型,采用HE染色、免疫组化、WB及流式细胞术检测中耳黏膜及脾脏淋巴细胞的变化及中耳黏膜PI3K/Akt/mTOR信号通路的变化。结果:分泌性中耳炎(OME)血清中细胞因子的表达和Th17特异性转录的ROR T和Treg特异性转录的Foxp3 mRNA的分析证实了Treg/Th17免疫失衡。OME大鼠模型进一步证实Treg/Th17失衡可导致OME,中耳粘膜染色及ROR T和Foxp3的表达证实了这一点。OME组和CON组中耳黏膜分别表达PI3K、Akt和mTOR蛋白。与CON组比较,OME组中耳黏膜P-MTOR、P-PI3K蛋白表达显著升高。结论:OME患者及OME动物模型均存在Treg/Th17失衡,其发病机制可能是全身性免疫反应异常,PI3K/Akt/mTOR信号被激活,T细胞分化异常,导致中耳黏膜充血、水肿,进而发生OME。
The Immune Imbalance of Treg/Th17 in Otitis Media of Effusion Patients May Be Related to PI3K/Akt/mTOR Signaling Activation in the Middle Ear Mucosa
Objective: To assess whether secretory otitis media may be caused by immune imbalance of Treg/Th17 mediated by PI3K/Akt/mTOR signaling, so as to find new therapeutic target.Methods: IL-17, TGF- and IL-6, IL-10 and Th17 cytokines were detected in peripheral blood of OME patients (PC group) and healthy people (NC group) by ELISA. The expression of ROR t mRNA and Foxp3mRNA in PBMC was detected by RT-PCR. OME rat model was established and the changes of lymphocytes in middle ear mucosa and spleen and PI3K/Akt/mTOR signaling in middle ear mucosa were detected by HE staining, IHC, WB and flow cytometry.Results: The immune imbalance of Treg/Th17 in secretory otitis media (OME) was confirmed by the expression of cytokines in OME serum and analysis of ROR T and Foxp3 mRNA which was Th17 and Treg specific transcription respectively. OME rat model further confirmed that Treg/Th17 imbalance could lead to OME as demonstrated by staining of MIDDLE ear mucosa and expression of ROR T and Foxp3. PI3K, Akt, and mTOR proteins were expressed in the MIDDLE ear mucosa of OME group and CON group, respectively. Compared with CON group, the expression of P-MTOR and P-PI3K proteins in the middle ear mucosa of OME group was significantly increased.Conclusions: Treg/Th17 imbalances are found in OME patients and OME animal model and the pathogenic mechanism may be due to systemic abnormal immune response, activated PI3K/Akt/mTOR signaling, abnormal T cell differentiation, leading to middle ear mucosal hyperemia, edema and subsequent occurrence of OME.