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Surface expression of anti‐CD3scfv stimulates locoregional immunotherapy against hepatocellular carcinoma depending on the E1A‐engineered human umbilical cord mesenchymal stem cells
Author(s) -
Zhang Qing,
Yuan XiangFei,
Lu Yang,
Li ZhenZhen,
Bao ShiQi,
Zhang XiaoLong,
Yang YuanYuan,
Fan DongMei,
Zhang YiZhi,
Wu ChenXuan,
Guo HongXing,
Zhang YanJun,
Ye Zhou,
Xiong DongSheng
Publication year - 2017
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.30846
Subject(s) - immunotherapy , antigen , cancer research , genetic enhancement , mesenchymal stem cell , hepatocellular carcinoma , cancer immunotherapy , biology , viral vector , immunology , immune system , gene , recombinant dna , microbiology and biotechnology , biochemistry
Tumor antigens is at the core of cancer immunotherapy, however, the ideal antigen selection is difficult especially in poorly immunogenic tumors. In this study, we designed a strategy to modify hepatocellular carcinoma (HCC) cells by surface expressing anti‐CD3scfv within the tumor site strictly, which depended on the E1A‐engineered human umbilical cord mesenchymal stem cells (HUMSC.E1A) delivery system. Subsequently, membrane‐bound anti‐CD3scfv actived the lymphocytes which lysed HCC cells bypassing the expression of antigens or MHC restriction. First, we constructed the anti‐CD3scfv gene driven by human α‐fetoprotein (AFP) promoter into an adenoviral vector and the E1A gene into the lentiviral vector. Our results showed that anti‐CD3scfv could specifically express on the surface of HCC cells and activate the lymphocytes to kill target cells effectively in vitro . HUMSC infected by AdCD3scfv followed by LentiR.E1A could support the adenoviral replication and packaging in vitro 36 h after LentiR.E1A infection. Using a subcutaneous HepG2 xenograft model, we confirmed that AdCD3scfv and LentiR.E1A co‐transfected HUMSC could migrate selectively to the tumor site and produce considerable adenoviruses. The new generated AdCD3scfv infected and modified tumor cells successfully. Mice injected with the MSC.E1A.AdCD3scfv and lymphocytes significantly inhibited the tumor growth compared with control groups. Furthermore, 5‐fluorouracil (5‐FU) could sensitize adenovirus infection at low MOI resulting in improved lymphocytes cytotoxicity in vitro and in vivo . In summary, this study provides a promising strategy for solid tumor immunotherapy.