首页 | 本学科首页   官方微博 | 高级检索  
检索        

三级淋巴器官(TLO)诱导形成及其在抗肿瘤免疫中的功能研究
引用本文:陈红,胡翔,张惠媛,胡洪波.三级淋巴器官(TLO)诱导形成及其在抗肿瘤免疫中的功能研究[J].四川大学学报(医学版),2022,53(1):35-42.
作者姓名:陈红  胡翔  张惠媛  胡洪波
作者单位:1.四川大学华西医院 生物治疗国家重点实验室 (成都 610041)
基金项目:国家自然科学基金(No.82025002、No.81871232)和科技部重点研发专项(No. 2019YFA0110200)资助
摘    要:目的 在体外诱导形成三级淋巴器官(tertiary lymphoid organs,TLO),并评价其在抗肿瘤免疫中的功能.方法 利用慢病毒系统在NIH3T3细胞上过表达淋巴毒素-β受体(lymphotoxin-beta receptor,LTβR),并检测LTβR-NIH3T3细胞中LTβR的过表达效率;通过免疫印迹...

关 键 词:三级淋巴器官  抗肿瘤免疫  非经典NF-κB信号通路
收稿时间:2021-09-26

Induction and Anti-Tumor Function of Tertiary Lymphoid Organs
CHEN Hong,HU Xiang,ZHANG Hui-yuan,HU Hong-bo.Induction and Anti-Tumor Function of Tertiary Lymphoid Organs[J].Journal of West China University of Medical Sciences,2022,53(1):35-42.
Authors:CHEN Hong  HU Xiang  ZHANG Hui-yuan  HU Hong-bo
Institution:1.State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu 610041, China
Abstract:  Objective  To induce the development of tertiary lymphoid organs (TLO) in a mouse model of melanoma and to evaluate TLO’s functions in antitumor immunity.  Methods  Lymphotoxin-beta receptor (LTβR) was overexpressed in NIH3T3 cells through the lentivirus system and the overexpression efficiency of LTβR in LTβR-NIH3T3 cells was examined. Western blot and qPCR were used to examine the non-canonical nuclear factor (NF)-κB signaling pathway in NIH3T3 cells overexpressing LTβR. B16-OVA melanoma mouse model was constructed to explore the induction of TLO and anti-tumor functions of TLO in LTβR-NIH3T3 cells.  Results  LTβR was overexpressed in NIH3T3 cells through the lentivirus system, and flow cytometry showed that the proportion of GFP+ cells reached 99%. The overexpression of LTβR activated the non-canonical NF-κB signaling pathway in NIH3T3 cells. Findings from the mouse tumor model suggest that the injection of LTβR-NIH3T3 cells successfully induced the development of lymphoid tissue around the tumor and enhanced the tumor infiltration of T cells and MHCⅡ+ macrophages, significantly inhibiting tumor growth and prolonging the survival of tumor-bearing mice.  Conclusion  LTβR-NIH3T3 cells promoted anti-tumor immunity by inducing TLO development, which may provide new perspectives for tumor immunotherapy.
Keywords:
点击此处可从《四川大学学报(医学版)》浏览原始摘要信息
点击此处可从《四川大学学报(医学版)》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号