Isolated T cell receptor, modified cell thereof, encoded nucleic acid and application thereof
A cell receptor and nucleic acid technology, applied in genetically modified cells, cells modified by introducing foreign genetic material, receptors/cell surface antigens/cell surface determinants, etc., to achieve good industrial application prospects and avoid immune rejection. , the effect of avoiding cytokine storm
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[0146] Preparation of recombinant TCR lentiviral expression vector: the viral vector used to express TCR is a replication-defective lentiviral vector, including: the lentiviral vector pCDH-EF1α-MCS-(PGK-GFP) expressing GFP, which can be purchased from System Biosciences (Cat#CD811A-1); and the vector pCDH-EF1α-MCS that does not express GFP, obtained by removing the PGK promoter and GFP gene on the pCDH-EF1α-MCS-(PGK-GFP) vector by using conventional techniques in the art. According to the obtained TCR gene sequence, synthesize the whole gene sequence of TCR β chain and α chain and the cleavable F2A sequence and Furin restriction fragment between them, and link to the multiple cloning site downstream of the EF-1α promoter of the vector , the sequence of transcription inserted into TCR is TCRβ chain (without stop codon), Furin fragment, F2A fragment, and TCRα chain (see the literature "Gene Ther. 2008 Nov; 15(21): 1411-1423"). The vector expressing GFP is driven by the inverted ...
Embodiment 1
[0149] Example 1: Induction of Her2 / neu 369-377 polypeptide (Her2-E75 epitope polypeptide) specific killer T cells from HLA-A2 positive normal donor peripheral blood
[0150] In this example, a low-concentration Her2 / neu 369-377 polypeptide of 1 μg / ml was used to induce polypeptide-specific killer T cells from HLA-A2-positive normal PBMC (#2) after two rounds of in vitro stimulation, and flow cytometric analysis was performed and single cell isolation. The specific method is as described above. The result is as follows:
[0151] figure 1 A The right figure shows that 0.024% of the lymphocytes are CD8-positive killer T cells that can bind to the Her2 / neu 369-377 / HLA-A2 pentamer (ie Her2-E75 pentamer), and the left figure does not pass through the Her2 polypeptide Stimulated control cells did not show CD8-positive pentamer-positive cells. The results showed that in the natural T cell pool, the number of specific T cells recognizing Her2 / neu 369-377 antigen polypeptide was ve...
Embodiment 2
[0152] Example 2: Obtaining the full sequence of Her2 / neu 369-377 polypeptide-specific TCR
[0153] This embodiment directly purifies total RNA from a certain number of Her2 CTL 6A5 cells obtained in Example 1, and obtains paired TCR α chain and β chain gene sequences by the method of 5'-RACE RT-PCR (that is, the two chains can be combined Consists of a functional TCR that recognizes antigenic polypeptides), and the encoded TCR is called "Her2 TCR-6A5". The amino acid sequence of the α chain of the TCR is shown in SEQ ID NO: 4, the coding sequence is shown in SEQ ID NO: 12, and the amino acid sequence of the β chain of the TCR is shown in SEQ ID NO: 7, and the coding sequence is shown in SEQ ID NO:15 shown. This TCR exists in the peripheral T cell pool of HLA-A2 positive normal people, and will not cross-react with normal cells that express Her2 / neu protein in a small amount and cause autoimmune reactions. To test the antigen specificity of the obtained TCR and its function,...
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