当细胞成为药物:一个南非的视角。

IF 1.2
I M Viljoen, M S Pepper
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引用次数: 1

摘要

人类白细胞抗原(HLA)的发现、血清学匹配和HLA分型技术,加上免疫抑制药物的发展和感染控制的改进,为细胞、组织和血管化器官移植开辟了道路。自20世纪60年代初以来,全世界已经进行了超过100万例造血祖细胞(HPC)移植,以恢复骨髓消融后的造血功能和支持免疫系统恢复。HPC移植使用最低限度的自体或异体细胞来恢复骨髓的同源功能。由新技术支持的生物科学研究越来越多地转化为旨在增强、修复、替换或再生体内基因、细胞、组织、器官和代谢过程的治疗产品。这些产品被称为再生医学疗法或先进治疗药物产品,包括基因疗法、细胞疗法和工程组织产品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
When cells become medicines: A South African perspective.

The discovery of human leucocyte antigen (HLA), serological matching and HLA-typing techniques, combined with the development of immunosuppressive medicines and improvements in infection control, have opened the way to cell, tissue and vascularised organ transplantation. Since the early 1960s, more than a million haematopoietic progenitor cell (HPC) transplantations have been performed worldwide to restore haematopoiesis and support immune system recovery after bone marrow ablation. HPC transplantation uses minimally manipulated autologous or allogeneic cells to restore the homologous functions of bone marrow. Research in biological sciences supported by new technologies is increasingly translated into therapeutic products intended to augment, repair, replace or regenerate genes, cells, tissues, organs and metabolic processes in the body. These products are referred to as regenerative medicine therapies or advanced therapy medicinal products, and include gene therapies, cell-based therapies and engineered tissue products.

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