Allogeneic antigen-presenting cell targeting kras mutation, construction method, and preparation method of intestinal cancer-specific CTL cells
A technology of allogeneic antigen and construction method, applied in the direction of genetically modified cells, cells modified by introducing foreign genetic material, animal cells, etc., can solve the problem of low proportion of specific cells, difficulty in benefiting patients with KRAS mutation, weak killing ability, etc. problem, to achieve a strong immune response
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[0032] The present invention also provides a method for preparing colon cancer-specific CTL cells, comprising the following steps: using the allogeneic antigen-presenting cells targeting KRAS mutations to co-culture T cells in peripheral blood mononuclear cells for 20-20~ On 22d, colon cancer-specific CTL cells were obtained. In the present invention, the peripheral blood mononuclear cells are derived from the intestinal cancer patient described in step 1) or the mononuclear cell provider described in step 3). The method for collecting the peripheral blood mononuclear cells is not particularly limited in the present invention, and a conventional method for collecting peripheral blood mononuclear cells in the art can be used (Ficoll-Pague, GE: 17544202). In the specific implementation of the present invention, there is no special limitation on the method for isolating T cells from the peripheral blood mononuclear cells, and conventional methods in the field can be used (Milteny...
Embodiment 1
[0036] Construction of a heterogeneous antigen-presenting cell targeting KRAS mutation
[0037] According to the patient's HLA typing results and KRAS mutation sequence, use the online prediction software NetMHCpan 4.0Server to analyze the affinity of all HLA typing and KRAS combinations, and sort them;
[0038] HLA typing includes: HLA-A0206, HLA-A2601, HLA-B4001, HLA-B1301, HLA-C0304, HLA-C0702
[0039] KRAS mutations include:
[0040] KRAS-12A: TEYKLVVVGAAGVGKSALTIQ (SEQ ID NO: 3)
[0041] KRAS-12C: TEYKLVVVGACGVGKSALTIQ (SEQ ID NO: 4)
[0042] KRAS-12D: TEYKLVVVGADGVGKSALTIQ (SEQ ID NO: 5)
[0043] KRAS-12S: TEYKLVVVGASGVGKSALTIQ (SEQ ID NO: 6)
[0044] KRAS-12V: TEYKLVVVGAVGVGKSALTIQ (SEQ ID NO: 7)
[0045] KRAS-13D: EYKLVVVGAGDVGKSALTIQL (SEQ ID NO: 8)
[0046] KRAS-61H: CLLDILDTAGHEEYSAMRDQY (SEQ ID NO: 9)
[0047] The combination of HLA typing and KRAS mutation antigen includes: HLA-A0206+KRAS-G12D, HLA-A0206+KRAS-G13D, HLA-A0206+KRAS-G12V, HLA-A0206+KRAS-G12C, ...
Embodiment 2
[0071] Colorectal cancer-specific CTL cells
[0072] 1. Isolation of T cells:
[0073] 1) Collect the patient's own PBMC by centrifugation, resuspend in PBS, pass the cells through a 30 μm cell sieve, and count;
[0074] 2) centrifuge at 300g for 10min, completely remove the supernatant;
[0075] 3) Resuspend the cells with separation buffer (PBS, pH 7.2, 0.5% BSA2mM EDTA), every 10 7 Cells were resuspended in 80 μL of separation buffer;
[0076] 4) Every 10 7 cells, add CD3 magnetic beads (Germany Miltenyi Biotechnology Co., Ltd.);
[0077] 5) After mixing, incubate for 15min (2-8°C)
[0078] 6) Every 10 7Add 1-2mL separation buffer to resuspend the cells, centrifuge at 300g for 10min, and completely remove the supernatant;
[0079] 7) will be 10 8 Resuspend cells within 500 μL of separation buffer;
[0080] 8) Rinse the separation column with separation buffer; MS: 500 μL, LS: 3 mL
[0081] 9) transfer the cells to the separation column;
[0082] 10) Collect unbou...
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