EGFR和PD-L1双靶向嵌合抗原受体构建及表达  

Construction and Expression of Chimeric Antigen Receptors Targeting Epidermal Growth Factor Receptor(EGFR)and Programmed Cell Death Ligand-1(PD-L1)

作　　者：李姝萍 ﹐王小珏 ﹐杨斌 ﹐王和林 ﹐闫卓红 易玲[1,2] ﹐韦攀健﹐金鑫郝建清 张洪涛[1,2] Li Shuping;Wang Xiaojue;Yang Bin;Wang Helin;Yan Zhuohong;YiLing;Wei Panjian;Jin Xin;Hao Jianqing;Zhang Hongtao(Central Laboratory,Beijing Tuberculosis and Thoracic Tumor Research Institute,Beijing 101149,China;Department of Tumor Immunology,Beijing Chest Hospital,Capital Medical University,Beijing 101149,China)

机构地区：[1]北京市结核病胸部肿瘤研究所中心实验室,101149 [2]首都医科大学附属北京胸科医院肿瘤免疫室,101149

出　　处：《结核病与胸部肿瘤》2020年第2期87-94,共8页Tuberculosis and Thoracic Tumor

基　　金：北京科技计划项目(Z1511004015104);北京卫计委肺癌诊断及生物治疗关键技术研究(PXM2018_026271_0002)。

摘　　要：目的构建肿瘤相关抗原表皮生长因子受体特异性嵌合抗原受体(EGFR-CAR)和程序性死亡受体-配体1(PD-L1)抗体双修饰慢病毒载体表达系统。方法人PD-L1-Fc蛋白免疫BALB/c小鼠,经细胞融合、亚克隆筛选高分泌PD-L1特异性抗体的稳定杂交瘤,酶联免疫吸附试验(ELISA)和Western blot检测抗体特异性,流式细胞术(FACS)鉴定对PD-1配受体封阻性能,Fortebio测定抗体亲和力抗体全长测序,经保留鼠源CRD1、CRD2和CRD3人源化改造后构建单链抗体(single-chain variable fragment,scFv);人EGFR单克隆抗体杂交瘤系,经5RACE技术扩增其轻链和重链可变区(VL和VH)基因,构建scFv,克隆至真核载体pcDNA3.1表达鉴定。基因合成EGFR-CAR(引入CD137协同信号胞内功能域)与PD-L1-scFv借助2A序列连接,克隆人慢病毒pLVX-EF1.-RES-ZsGreen1表达载体,使用Lent-X Packagng Singie Shots(VSV-G)共同转染293T细胞,获得包装病毒,感染293V细胞,FACS测定CAR膜表达,ELISA检测CAR感染293V细胞培养上清中PD-L1l-scFv表达情况,转染激活人外周血T细胞,验证CAR膜表达。结果获得PD-L1抗体11E3,具备高度配受体封阻性能,经人源化改造后,亲和力稳定(2.67×10^-10 molL),EGFR-scFv获得有效表达。进一步构建了EGFR-CAR和PD-L1双修饰慢病毒分泌型CAR(CTCO537-1)及膜表达型CAR(CTC0537-2),其病毒感染293V细胞阳性率为10%。CTZ0431-1感染293V细胞后,细胞膜表面表达EGFR-scFv,检测培养上清存在PD-L1-SeFv;CTZ0431-2感染293V细胞后,细胞膜表面EGFR-scFv和PD-L1-scFv有效表达,双表达病毒感染活化T细胞的CAR表达率为39.3%。结论成功构建了EGFR-CAR和PD-L1-scFv双表达慢病毒载体,EGFR-CAR中度结合亲和力,此为EGFR靶向和PD-L1抗体双修饰CAR-T细胞的实体瘤治疗研究提供了关键工具。Objective To construct an expression system of lentivirus vector encoding epidermal growth factor receptor-specific chimerio antigen receptor(EGFR-CAR)and programmed cell death ligand-l(PD-L1)antibody.MethodsHuman PD-L1-e protein was used to immunize BALB/c mic.Cell-fusion and subcloning were performed to screen stable bybridoma strains with high secretion of PD-Ll-specific antibodies,which were identified by both ELISA and Westerm blot.The activity of the antibodies in blocking the binding of programmed cell death-1(PD-1)to PD-Ll was determined by fuorescence-activated cell sorting(FACS).Antibody affnity was analyzed by Fortebio Oecte96.Asingle-chain variable fragment(scFv)was further constructed after antibody fll-length sequencing and humanization using CDRgrating method.Meanwhile,the genes encoding the light and heavy chain variable regions(VLand VH)were cloned from a byoridoma secreting antibody against human EGFR by 5'RACE'tocinology to constuct scFv gene.The expression of scFv was confirmed using peDNA3.1 vector.EGFR-CAR containing CD137 intraclltarfunction domain and PD-Ll-scPFv was ligated using 2A gene.The synthetic single molecule was cloned into pLVXEF1a-RES-ZsGreeal lentivirus oxprssion vector,and the transfected into 293T cells using Lenti-X Packaging Single Shots(VSV-G)to prepare infectious virus.Expression of CAR on cll surface and the sohuble fomo&PD-Ll-scFv in the supernatant of transfected 293V cellswere detected by FACS andELISA.Results APD-L1 antibody named 11E3 with high ligand-receptor blocking performance was obtained.The humanized antibody showed a stable affinity(2.67×10^-10mol L)after dirctly gratting the mousoCDRs(CDR1,CDR2 and CDR3)to buman frameworkS.EGFR-scFv was effctively expressed in a form of Fo-fusion.Secretory CAR(CTZ0431-1)and membrane CAR(CTZ0431-2)expression plasmids were constructed using lentivirus vector contining EGFR-CAR and PD-L1-scFv.The infection eficiency in 293V clls was around 10%.EGFR-scFv on the cell membranes and PD-Ll-scfv in the culture supernatats were det

关 键 词：EGFR-CAR PD-LI-scFv 膜表达型 分泌表达型 合成生物技术 

分 类 号：R73[医药卫生—肿瘤]