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Current Status of Gene Engineering Cell Therapeutics

机译:基因工程细胞治疗的现状

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摘要

Ex vivo manipulations of autologous patient’s cells or gene-engineered cell therapeutics have allowed the development of cell and gene therapy approaches to treat otherwise incurable diseases. These modalities of personalized medicine have already shown great promises including product commercialization for some rare diseases. The transfer of a chimeric antigen receptor or T cell receptor genes into autologous T cells has led to very promising outcomes for some cancers, and particularly for hematological malignancies. In addition, gene-engineered cell therapeutics are also being explored to induce tolerance and regulate inflammation. Here, we review the latest gene-engineered cell therapeutic approaches being currently explored to induce an efficient immune response against cancer cells or viruses by engineering T cells, natural killer cells, gamma delta T cells, or cytokine-induced killer cells and to modulate inflammation using regulatory T cells.
机译:自体患者细胞的离体操作或基因工程化的细胞疗法已经发展出细胞和基因疗法来治疗原本无法治愈的疾病。这些个性化医学的方式已经显示出巨大的希望,包括一些罕见疾病的产品商业化。嵌合抗原受体或T细胞受体基因转移到自体T细胞中已导致某些癌症,尤其是血液系统恶性肿瘤的非常有希望的结果。另外,基因工程细胞治疗剂也正在探索以诱导耐受性和调节炎症。在这里,我们回顾了目前正在探索的最新基因工程细胞治疗方法,该方法可通过工程改造T细胞,自然杀伤细胞,γ-δT细胞或细胞因子诱导的杀伤细胞来诱导针对癌细胞或病毒的有效免疫应答,并调节炎症使用调节性T细胞。

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