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CTLA-4-targeting trans-splicing ribozyme for delivery of chimeric antigen receptor, and use thereof

机译:用于递送嵌合抗原受体的ctla-4靶向转拼核酶及其用途

摘要

The present invention relates to a recombinant vector, characterized by including a cytotoxic T-lymphocyte-associated protein-4 (CTLA-4)-targeting trans-splicing ribozyme expression cassette for delivery of chimeric antigen receptor, wherein the expression cassette includes: (i) a CTLA-4-targeting trans-splicing ribozyme; and (ii) a polynucleotide encoding a chimeric antigen receptor ligated to the 3′ exon of the ribozyme. The present invention also relates to a transformed cell into which the recombinant vector is introduced, a ribozyme expressed from the recombinant vector, a retrovirus expressing the ribozyme, and a T cell treated with the retrovirus. Furthermore, the present invention relates to a pharmaceutical composition for preventing or treating cancers, in which the pharmaceutical composition includes the recombinant vector, the transformed cell, the ribozyme, the retrovirus, the T cell, or a combination thereof; and a method for treating cancers, in which the method includes administering, to an individual in need thereof, the recombinant vector, the transformed cell, the ribozyme, the retrovirus, the T cell, or a combination thereof. The recombinant vector of the present invention and the ribozyme expressed therefrom become a gene-cell therapy which inhibits CTLA-4 on T cells which has been an obstacle in conventional anti-cancer therapies and, at the same time, enables anti-cancer treatment, thereby allowing more effective anti-cancer effects to be anticipated. Such a gene-cell therapy results in decreased toxicity in normal tissues and thus exhibits increased effects in both therapeutic efficacy and safety, which enables it to be widely utilized in the field of gene therapy in the future.
机译:本发明涉及一种重组载体,其特征在于包括用于递送嵌合抗原受体的靶向细胞毒性T淋巴细胞相关蛋白4(CTLA-4)的反式拼接核酶表达盒,其中所述表达盒包括: )CTLA-4靶向转拼核酶; (ii)与嵌合酶的3'外显子连接的编码嵌合抗原受体的多核苷酸。本发明还涉及导入了重组载体的转化细胞,由重组载体表达的核酶,表达核酶的逆转录病毒以及用逆转录病毒处理的T细胞。此外,本发明涉及用于预防或治疗癌症的药物组合物,其中所述药物组合物包括重组载体,转化的细胞,核酶,逆转录病毒,T细胞或其组合;和以及治疗癌症的方法,其中该方法包括对有需要的个体施用重组载体,转化的细胞,核酶,逆转录病毒,T细胞或其组合。本发明的重组载体和由其表达的核酶成为一种基因细胞疗法,可抑制T细胞上的CTLA-4,这已成为常规抗癌疗法的障碍,同时可进行抗癌治疗,从而可以预期更有效的抗癌作用。这样的基因细胞疗法导致对正常组织的毒性降低,因此在治疗功效和安全性方面均显示出增加的效果,这使得其将来可以在基因疗法领域中广泛使用。

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