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输注基因编辑异体嵌合抗原受体 T 细胞后染色体改变的检测。

Detection of chromosomal alteration after infusion of gene-edited allogeneic CAR T cells.

机构信息

Allogene Therapeutics, South San Francisco, CA 94080, USA.

Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Mol Ther. 2023 Mar 1;31(3):676-685. doi: 10.1016/j.ymthe.2022.12.004. Epub 2022 Dec 14.

Abstract

A chromosome 14 inversion was found in a patient who developed bone marrow aplasia following treatment with allogeneic chimeric antigen receptor (CAR) Tcells containing gene edits made with transcription activator-like effector nucleases (TALEN). TALEN editing sites were not involved at either breakpoint. Recombination signal sequences (RSSs) were found suggesting recombination-activating gene (RAG)-mediated activity. The inversion represented a dominant clone detected in the context of decreasing absolute CAR Tcell and overall lymphocyte counts. The inversion was not associated with clinical consequences and wasnot detected in the drug product administered to this patient or in any drug product used in this or other trials using the same manufacturing processes. Neither was the inversion detected in this patient at earlier time points or in any other patient enrolled in this or other trials treated with this or other product lots. This case illustrates that spontaneous, possibly RAG-mediated, recombination events unrelated to gene editing can occur in adoptive cell therapy studies, emphasizes the need for ruling out off-target gene editing sites, and illustrates that other processes, such as spontaneous V(D)J recombination, can lead to chromosomal alterations in infused cells independent of gene editing.

摘要

在接受含有转录激活因子样效应物核酸酶(TALEN)基因编辑的同种异体嵌合抗原受体(CAR)T 细胞治疗后发生骨髓再生障碍的患者中发现了 14 号染色体倒位。TALEN 编辑位点在两个断点处均未涉及。发现了重组信号序列(RSS),提示重组激活基因(RAG)介导的活性。该倒位代表在绝对 CAR T 细胞和总淋巴细胞计数下降的情况下检测到的显性克隆。该倒位与临床后果无关,也未在给予该患者的药物产品中或在使用相同制造工艺的本或其他试验中使用的任何药物产品中检测到。在该患者的早期时间点或在接受本或其他试验中使用的本或其他产品批次治疗的任何其他患者中也未检测到该倒位。该病例说明,在过继细胞治疗研究中可能与基因编辑无关的自发、可能由 RAG 介导的重组事件会发生,强调需要排除脱靶基因编辑位点,并说明其他过程,如自发 V(D)J 重组,可导致输注细胞发生染色体改变,而与基因编辑无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a65e/10014221/76aa3747dc7f/fx1.jpg

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