A preparation method for enhancing the lethality of tumor-infiltrating lymphocytes
A technology of lymphocyte and tumor infiltration, applied in the field of preparation of anti-tumor cells, can solve the problems of limiting the clinical application and toxicity of TIL therapy
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[0045] The invention provides a preparation method of infiltrating lymphocytes, which is specifically as follows:
[0046] 1) Preparation of recombinant lentivirus containing the gene of interest;
[0047] Specifically: obtaining and optimizing the synthesis of IL-7 sequence, IL-15 sequence and IL-7-IL-15 fusion sequence, inserting the sequence into a lentiviral vector, and then transfecting HEK-293T cells for virus preparation and amplification, and after culturing Obtain recombinant lentivirus;
[0048] Wherein, the IL-7 sequence is shown in SEQ ID No: 1; the IL-15 sequence is shown in SEQ ID No: 2; the IL-7-IL-15 fusion sequence is shown in SEQ ID No: 3 Show;
[0049] 2) After the tumor tissue was digested, a single cell suspension was obtained, and the single cell suspension was cultured with IL-2 to separate and purify the infiltrating lymphocytes; then in a culture environment coated with recombinant human fibrin and CD3 antibody, purified IL-2 was added to the infilt...
Embodiment 1
[0052] Example 1 Construction of lentiviral expression vectors of IL-7, IL-15 and IL-7-IL-15 genes
[0053] 1. Construction of plasmid containing IL-7 or IL-15 or IL-7-IL-15 gene
[0054] Download the CDS sequences of IL-7 and IL-15 from NCBI, and then perform codon optimization to enhance their expression. These optimization methods include but are not limited to: human codon usage preference, moderate GC content, stable mRNA secondary structure, etc., eliminate repetitive sequences and cryptic splice sites and unwanted restriction sites while preventing depletion of the tRNA pool in the cell. The optimized sequence was directly used for gene synthesis, and the ECoRI and BamHI restriction sites were used to connect the Tet-on expression plasmid pLVX-TetOne-Puro with the same double restriction. The plasmids verified by restriction digestion and sequencing were named pLVX-IL-7, pLVX-IL-15 and pLVX-IL-7-IL15, respectively. IRES is used to connect IL-7 and IL-15. IRES is an i...
Embodiment 2
[0060] Example 2 Preparation of non-small cell lung cancer TIL cells
[0061] 1. Tissue pretreatment: Tumor tissue sample collection tubes, reagents, operating instruments, etc. are wiped with 75% ethanol and placed in a biological safety cabinet. Open the tumor tissue sample collection bottle in the biological safety cabinet, wash the tumor tissue, and remove blood vessels. , capsule and other necrotic tissue.
[0062] 2. Tissue digestion:
[0063] 1) Mince the tumor tissue in the tissue enzymolysis solution to a near-meat-like shape, add the tissue enzymolysis solution to suspend, transfer the suspension to a centrifuge tube, put it into an electrothermal constant temperature shaker, set the temperature to 37°C, and set the shaking frequency to 150rpm / min, time 30-60min, constant temperature digestion.
[0064] 2) Take 40mL of stop protection solution and put it in a 50mL centrifuge tube for use, take a 70µm filter and place it at the mouth of the 50mL centrifuge tube, an...
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