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工程化T细胞力量的另一面:基因改造T细胞作为治疗手段的已观察到的和潜在的毒性

The Flipside of the Power of Engineered T Cells: Observed and Potential Toxicities of Genetically Modified T Cells as Therapy.

作者信息

Bedoya Felipe, Frigault Matthew J, Maus Marcela V

机构信息

Cellular Immunotherapy Program, Cancer Center, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.

Cellular Immunotherapy Program, Cancer Center, Massachusetts General Hospital, Boston, MA 02114, USA; Harvard Medical School, Boston, MA 02115, USA.

出版信息

Mol Ther. 2017 Feb 1;25(2):314-320. doi: 10.1016/j.ymthe.2016.11.011.

DOI:10.1016/j.ymthe.2016.11.011
PMID:28153085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5368422/
Abstract

Autologous T cells modified to recognize novel antigen targets are a novel form of therapy for cancer. We review the various potential forms of observed and hypothetical toxicities associated with genetically modified T cells. Despite the focus on toxicities in this review, re-directed T cells represent a powerful and highly effective form of anti-cancer therapy; we remain optimistic that the common toxicities will become routinely manageable and that some theoretical toxicity will be exceedingly rare, if ever observed.

摘要

经过改造以识别新型抗原靶点的自体T细胞是一种新型癌症治疗方法。我们综述了与基因改造T细胞相关的各种已观察到的和假设的潜在毒性形式。尽管本综述重点关注毒性,但重定向T细胞代表了一种强大且高效的抗癌治疗形式;我们仍然乐观地认为,常见毒性将变得常规可控,并且一些理论上的毒性即使被观察到也将极其罕见。

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本文引用的文献

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Toxicity and management in CAR T-cell therapy.嵌合抗原受体 T 细胞疗法的毒性与管理。
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Current tools for predicting cancer-specific T cell immunity.目前用于预测癌症特异性T细胞免疫的工具。
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Autologous T Cells Expressing CD30 Chimeric Antigen Receptors for Relapsed or Refractory Hodgkin Lymphoma: An Open-Label Phase I Trial.表达 CD30 嵌合抗原受体的自体 T 细胞治疗复发或难治性霍奇金淋巴瘤的开放性 I 期临床试验。
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Clinical responses with T lymphocytes targeting malignancy-associated κ light chains.针对恶性肿瘤相关κ轻链的T淋巴细胞的临床反应。
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