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Use of chimeric antigen receptor NK-92 cells to target mesothelin in ovarian cancer

Biochem Biophys Res Commun. 2020; 
Cao B, Liu M, Wang L, Liang B, Feng Y, Chen X, Shi Y, Zhang J, Ye X, Tian Y, Zhi C, Li J, Lian H, Wu Q, Zhang Z.
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Gene Synthesis Genes and lentiviral vectors To generate CAR-targeting molecules, the genes of anti-MSLN scFv [16] and anti-CD19 scFv, combined with CD8 leader, CD8 hinge, CD28 transmembrane, and composite CD28-CD137-CD3z intracellular signaling domains, under the control of an EF-1a promoter, were synthesized by Genscript Co. Get A Quote

摘要

Mesothelin (MSLN) has been reported to be overexpressed in ovarian cancer and may be an ideal target for immunotherapy. Recent studies have suggested that natural killer (NK) cells may be better chimeric antigen receptor (CAR) drivers because of their favorable innate characteristics, such as directly recognizing and killing tumor cells, resulting in a graft-versus-tumor effect but irresponsible for graft-versus-host disease (GVHD). The therapeutic effects of CAR-engineered NK cells targeting MSLN in ovarian cancer have not been evaluated. In this study, MSLN- and CD19-targeted CAR NK-92 (MSLN- and CD19-CAR NK) cells were constructed. Both MSLN- and CD19-CAR molecules were highly expressed on the surface of NK-... More

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