癌症的过继免疫治疗:T细胞特异性的基因转移。

Amir A Al-Khami, Shikhar Mehrotra, Michael I Nishimura
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引用次数: 14

摘要

肿瘤反应性T细胞的过继性转移已成为肿瘤免疫治疗的一个有前途的进展。具体来说,肿瘤浸润淋巴细胞的输注为转移性黑色素瘤患者带来了长期客观的临床反应。供体淋巴细胞输注也是移植后淋巴细胞增生性疾病的有效治疗方法。然而,过继T细胞疗法在大量患者的抗原特异性淋巴细胞的分离和扩增方面存在限制。规避这一限制并将过继免疫疗法扩展到其他癌症类型的一种方法是对具有抗原特异性受体的T细胞进行遗传修饰。在本文中,我们回顾了定向T细胞特异性的策略,包括T细胞受体基因转移和抗体受体基因转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adoptive immunotherapy of cancer: Gene transfer of T cell specificity.

Adoptive transfer of tumor-reactive T cells has emerged as a promising advance in tumor immunotherapy. Specifically, infusion of tumor-infiltrating lymphocytes has led to long-term objective clinical responses for patients with metastatic melanoma. Donor lymphocyte infusion is also an effective treatment of post-transplant lymphoproliferative disease. However, adoptive T cell therapy has restrictions in the isolation and expansion of antigen-specific lymphocytes for a large group of patients. One approach to circumvent this limitation and extend adoptive immunotherapy to other cancer types is the genetic modification of T cells with antigen-specific receptors. In this article, we review strategies to redirect T cell specificity, including T cell receptor gene transfer and antibody receptor gene transfer.

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