Chimeric antigen receptor, gene thereof and recombinant expression vector of gene as well as CARMSLN-NKT cell and preparation method and application of CARMSLN-NKT cell
A chimeric antigen receptor and NKT cell technology, applied in the field of tumor biological products, can solve the problems of insufficient distribution of MSLN monoclonal antibody and transient targeting effect of MSLN monoclonal antibody, achieve good industrial application prospects and enhance specific killing Active, power-enhancing effects
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[0027] The preparation method of the lentiviral expression vector PWPT-MSLNScFv-CD8-CD137-CD3ζ is not particularly limited, and can be various methods that can be imagined by those skilled in the art. Preferably, the lentiviral expression vector PWPT-MSLNScFv-CD8-CD137 -The preparation method of CD3ζ comprises the following steps:
[0028] (1) The hinge region and transmembrane region of CD8, the intracellular signaling domain of CD137 and the intracellular signaling domain of CD3ζ were respectively amplified from NKT cell cDNA, and cloned into the vector PWPT-GFP to construct PWPT-CD8 - CD137-CD3ζ;
[0029] (2) The nucleotide sequences encoding CD8a signal peptide and MSLNScFv were synthesized and cloned into PWPT-CD8-CD137-CD3ζ, and the correct sequence of PWPT-MSLNScFv-CD8-CD137-CD3ζ was obtained after sequencing verification.
[0030] In step (1), there is no particular limitation on the methods for respectively amplifying the hinge region and transmembrane region of CD8,...
Embodiment 1
[0082] Example 1 Preparation of NKT cells
[0083] (1) Take human venous blood in a vacuum tube containing heparin. Mononuclear cells (PBMCs) were obtained by density gradient centrifugation using lymphocyte separation medium.
[0084] (2) After PBMCs were washed three times, the final concentration of cells was adjusted to 2×10 by using NKT cell culture medium GT-T551 containing 0.6 volume % human autologous serum. 6 cells / mL; the cells were inoculated on a 75 cm 2 in cell culture flasks. Then add recombinant human interleukin-2 with a final concentration of 500U / mL, 50ng / ml CD3 monoclonal antibody and 50ng / mL recombinant human interleukin-15 to the culture medium, at 37°C and saturated humidity of 5% CO 2 cultured in an incubator.
[0085] (3) On the 4th day of culture, transfer the cells to an uncoated culture flask, add NKT cell culture medium GT-T551 every 2 days according to the number of cell growth, and control the cell concentration to 1×10 8 cells / mL, and added ...
Embodiment 2
[0086] Example 2 Construction of lentiviral expression vector PWPT-MSLNScFv-CD8-CD137-CD3ζ
[0087] (1) Preparation of NKT cell cDNA
[0088] The NKT cells cultured in Example 1 were centrifuged to precipitate, and the total RNA of the cells was extracted with RNAiso Reagent, a total RNA extraction kit, and stored at -80°C for future use. Extracted total RNA with RevertAid Reverse Transcription Kit TM NKT cell cDNA was obtained by reverse transcription with the First StrandcDNA Synthesis Kit, and stored at -20°C for future use.
[0089] (2) Preparation of lentiviral plasmid PWPT-CD8-CD137-CD3ζ
[0090] The following primer sequences were designed and synthesized (wherein, the underline marks are protected bases, and the square boxes are enzyme cleavage sites):
[0091]
[0092]
[0093] Using NKT cell cDNA in step (1) as a template, PCR amplification was carried out with primers P1 and P2 to obtain the hinge region and shortened transmembrane region of CD8 with a len...
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