Construction and Optimization of CD19 Chimeric Antigen Receptor T Cells Derived from C57BL/6J Mice
Objective:To explore the stimulation conditions,optimal culture time and infection time of C57BL/6J mice CD3+T cells in vitro,so as to improve the infection efficiency of CD 19 chimeric antigen receptor T cells(mCD19 CAR-T).Methods:Purified C57BL/6J mice CD3+T cells were cultured in anti-CD3/CD28 coated,anti-CD3 coated+soluble anti-CD28 and anti-CD3 coated,respectively.The cells were stimulated in above three conditions for 12 h and 24 h,following with 24 h,48 h and 72 h incubation and then the number of cell clones was recorded.C57BL/6J mice CD3+T cells were stimulated for 12 h,24 h,and 36 h under the above three conditions,then interleukin(IL)-2(100 U/ml)was added.The number of cell clones was recorded under microscope at 24 h,48 h,and 72 h of culture.After 24 h of stimulation,CD3+T cells derived from C57BL/6J mice were infected with retrovirus for 48 h to establish mCD19 CAR-T cells,and the percentage of GFP+CAR-T cells was detected by flow cytometry.Results:The infection efficiency of mCD19 CAR-T cells derived from C57BL/6J mice was only 5.23％under the optimized conditions of mCD19 CAR-T cells derived from BALB/c mice.The number of clones of C57BL/6J mice CD3+T cells was the highest in anti-CD3 coated+soluble anti-CD28 group after stimulated for 24 h and followed cultured for 48 h.After 24 hours of stimulation under the above conditions and 48 hours of culture with IL-2,the number of T cell proliferating clones in the anti-CD3 coated+soluble anti-CD28 group was significantly increased compared with the same group without IL-2,and the infection efficiency of CAR-T cells in this group reached 17.63％±4.17％.Conclusion:The optimal conditions for constructing CAR-T cells from C57BL/6J mice CD3+T cells are different from those of BABL/c mice.T cells stimulated by anti-CD3 coated+soluble anti-CD28+IL-2 can obtain mCD19 CAR-T cells with the highest efficiency after retrovirus infection.
万方数据
维普
