首页> 外文期刊>Journal of immunology research. >Third-Generation Anti-CD47-Specific CAR-T Cells Effectively Kill Cancer Cells and Reduce the Genes Expression in Lung Cancer Cell Metastasis
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Third-Generation Anti-CD47-Specific CAR-T Cells Effectively Kill Cancer Cells and Reduce the Genes Expression in Lung Cancer Cell Metastasis

机译:第三代抗CD47特异性CAR-T细胞有效杀死癌细胞并降低肺癌细胞转移中的基因表达

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CD47 is a cell surface glycoprotein molecule, belonging to the immunoglobulin superfamily, binding to various proteins including integrins, thrombospondin-1, and signal regulatory protein α (SIRP α ). CD47 is an important tumor antigen for the development and progression of various cancers. This study designed the chimeric antigen receptor T-cell (CAR-T) to bind to the CD47 to inhibit the expression of CD47. We used the complementarity-determining regions (CDRs) of the B6H12 mouse antibody grafted onto the IgG1 framework to create the humanized single-chain variable fragment (scFv) with linker (G4S)x3. scFv was used to design the chimeric antigen receptor with the structure CD8signal-CD47scFv-CD8a hinge-CD4TM-CD28-41BB-CD3 ζ , which was then transformed into T lymphocytes by the lentivirus to create third generation of CAR-T. Results revealed that the new CAR-T cells efficiently killed A549 cancer cells. CAR-T inhibited the expression of genes involved in metastasis and invasion of cells A549 including beta actin, calreticulin, and cyclooxygenase 2 at mRNA levels.
机译:CD47是一种细胞表面糖蛋白分子,属于免疫球蛋白超家族,与各种蛋白质结合,包括整联蛋白,血小板活力蛋白-1和信号调节蛋白α(siRPα)。 CD47是各种癌症的开发和进展的重要肿瘤抗原。该研究设计了嵌合抗原受体T细胞(CAR-T)与CD47结合以抑制CD47的表达。我们使用嫁接到IgG1框架上的B6H12小鼠抗体的互补确定区域(CDRS)以用接头(G4s)X3产生人源化单链可变片段(SCFV)。 SCV用于设计嵌合抗原受体的结构CD8Signal-CD47SCFV-CD8A铰链-CD4TM-CD28-41BB-CD3β,然后通过慢病毒转化成T淋巴细胞以产生第三代CAR-T。结果表明,新的CAR-T细胞有效地杀死了A549癌细胞。 Car-T抑制了在mRNA水平下包括β肌动蛋白,钙霉素和环氧氢酶2的细胞A549中参与转移和侵袭的基因的表达。

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