HLA-G specific chimeric antigen receptor, nucleic acid encoding HLA-G specific chimeric antigen receptor, expression plastid of HLA-G specific chimeric antigen receptor, cell expressing HLA-G specific chimeric antigen receptor, application of cell and composition
A chimeric antigen receptor, HLA-G technology, applied in nucleic acid encoding chimeric antigen receptors, pharmaceutical compositions for treating cancer, chimeric antigen receptors, and cells expressing chimeric antigen receptors, can solve intractable problems Overcoming solid tumor immunosuppressive microenvironment, inefficient immune cells, and chimeric antigen receptor efficacy limitations
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Embodiment 1
[0039] In this test example, the HLA-G-specific chimeric antigen receptor of the present invention is transduced into primary natural killer cells to obtain the HLA-G-specific chimeric antigen receptor-expressing cells of Example 1 of the present invention (hereinafter It is referred to as Example 1) for short. And the effect of Example 1 and the pharmaceutical composition for treating cancer containing Example 1 in inducing the death of breast cancer cells, glioblastoma multiforme cells, pancreatic cancer cells and ovarian cancer cells was further tested.
[0040] Firstly, human breast cancer cell line MDA-MB-231, human malignant brain tumor cell line DBTRG, human pancreatic cancer cell line AsPC1 and human ovarian cancer cell line SKOV3 were mixed with 1×10 5 The density of cells / well was seeded in 12-well plates, and the experiment was performed after culturing for 48 hours. In the experiment, each tumor cell was divided into 6 groups, which were untreated control group, e...
Embodiment 2
[0048] In this test example, the HLA-G-specific chimeric antigen receptor expressing cell of the present invention Example 2 (hereinafter referred to as For example 2). And the effect of Example 2 and the pharmaceutical composition for treating cancer comprising Example 2 in inducing the death of breast cancer cells, glioblastoma multiforme cells, pancreatic cancer cells and ovarian cancer cells was further tested.
[0049] Firstly, human breast cancer cell line MDA-MB-231, human malignant brain tumor cell line DBTRG, human pancreatic cancer cell line AsPC1 and human ovarian cancer cell line SKOV3 were mixed with 1×10 5 The density of cells / well was seeded in 12-well plates, and the experiment was performed after culturing for 48 hours. In the experiment, each tumor cell was divided into 6 groups, namely the untreated control group, the experimental group 1 treated with chemotherapy drugs, the experimental group 2 treated with parental primary T cells, and the experimental gr...
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