Chimeric antigen receptor T cell targeting EGFRvIII for metastatic lung cancer therapy

嵌合抗原受体 癌症研究 抗原 生物 表皮生长因子受体 免疫疗法 T细胞 分子生物学 癌症 病毒学 免疫学 免疫系统 遗传学
作者
Zhao Zhang,Jun Jiang,Xiaodong Wu,Mengyao Zhang,Dan Luo,Renyu Zhang,Shiyou Li,You‐Wen He,Huijie Bian,Zhi‐Nan Chen
出处
期刊:Frontiers of Medicine [Higher Education Press]
卷期号:13 (1): 57-68 被引量:39
标识
DOI:10.1007/s11684-019-0683-y
摘要

Lung cancer is the most common incident cancer and the leading cause of cancer death. In recent years, the development of tumor immunotherapy especially chimeric antigen receptor T (CAR-T) cell has shown a promising future. Epidermal growth factor receptor variant III (EGFRvIII) is a tumor-specific mutation expressed in various types of tumors and has been detected in non-small cell lung cancer with a mutation rate of 10%. Thus, EGFRvIII is a potential antigen for targeted lung cancer therapy. In this study, CAR vectors were constructed and transfected into virus-packaging cells. Then, activated T cells were infected with retrovirus harvested from stable virus-producing single clone cell lines. CAR expression on the surfaces of the T cells was detected by flow cytometry and Western blot. The function of CAR-T targeting EGFRvIII was then evaluated. The EGFRvIII-CAR vector was successfully constructed and confirmed by DNA sequencing. A stable virus-producing cell line was produced from a single clone by limited dilution. The culture conditions for the cell line, including cell density, temperature, and culture medium were optimized. After infection with retrovirus, CAR was expressed on more than 90% of the T cells. The proliferation of CAR-T cells were induced by cytokine and specific antigen in vitro. More importantly, EGFRvIII-CART specifically and efficiently recognized and killed A549-EGFRvIII cells with an effector/target ratio of 10:1 by expressing and releasing cytokines, including perforin, granzyme B, IFN-γ, and TNF-α. The in vivo study indicated that the metastasis of A549-EGFRvIII cells in mice were inhibited by EGFRvIII-CART cells, and the survival of the mice was significantly prolonged with no serious side effects. EGFRvIII-CART showed significantly efficient antitumor activity against lung cancer cells expressing EGFRvIII in vivo and in vitro. Therefore, CAR-T targeting EGFRvIII is a potential therapeutic strategy in preventing recurrence and metastasis of lung cancer after surgery.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
JackLiu完成签到,获得积分10
1秒前
完美世界应助Lupin采纳,获得10
1秒前
LLLpqqq完成签到,获得积分10
1秒前
1秒前
J_B_Zhao完成签到 ,获得积分10
2秒前
鳗鱼蹇完成签到,获得积分10
2秒前
ginchuodan发布了新的文献求助10
2秒前
2秒前
Winfred应助卡卡卡采纳,获得10
2秒前
4秒前
xixixii发布了新的文献求助10
4秒前
RimutO0530发布了新的文献求助10
4秒前
玉七发布了新的文献求助10
4秒前
思源应助小橘子采纳,获得10
4秒前
易楠发布了新的文献求助10
5秒前
5秒前
木易完成签到,获得积分10
6秒前
6秒前
sweet发布了新的文献求助10
7秒前
笨笨如之发布了新的文献求助10
7秒前
13728891737发布了新的文献求助30
7秒前
7秒前
木子不甜完成签到,获得积分10
7秒前
英姑应助不喜采纳,获得10
8秒前
8秒前
71333197发布了新的文献求助10
8秒前
9秒前
10秒前
jjj完成签到,获得积分10
10秒前
选民很头疼完成签到,获得积分10
11秒前
hitagi发布了新的文献求助10
11秒前
端庄梦松发布了新的文献求助10
11秒前
12秒前
12秒前
酷波er应助易楠采纳,获得10
12秒前
要苦就苦别人完成签到,获得积分10
12秒前
12秒前
jqian发布了新的文献求助30
13秒前
高分求助中
卤化钙钛矿人工突触的研究 1000
Engineering for calcareous sediments : proceedings of the International Conference on Calcareous Sediments, Perth 15-18 March 1988 / edited by R.J. Jewell, D.C. Andrews 1000
Wolffs Headache and Other Head Pain 9th Edition 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 510
Cardiac structure and function of elite volleyball players across different playing positions 500
CLSI H26-A2 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6241558
求助须知:如何正确求助?哪些是违规求助? 8065545
关于积分的说明 16833691
捐赠科研通 5319893
什么是DOI,文献DOI怎么找? 2832841
邀请新用户注册赠送积分活动 1810242
关于科研通互助平台的介绍 1666772