靶异构体是嵌合抗原受体细胞治疗中被忽视的挑战和机遇。

IF 4.1 Q2 IMMUNOLOGY
Immunotherapy advances Pub Date : 2022-04-20 eCollection Date: 2022-01-01 DOI:10.1093/immadv/ltac009
Mike Bogetofte Barnkob, Kristoffer Vitting-Seerup, Lars Rønn Olsen
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引用次数: 8

摘要

新型嵌合抗原受体(CAR)细胞疗法的发展正在迅速发展,今年到目前为止,已有299种新药被报道,109种新的临床试验开始。从已批准的cd19特异性CAR疗法中得到的一个重要教训是,靶标异构体转换已被证明会导致肿瘤复发,但对实体癌中CAR靶标的异构体知之甚少。在这里,我们评估了蛋白质异构体景观,并确定了当CAR治疗应用于实体癌症时蛋白质异构体转换存在的挑战和机遇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy.

Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy.

Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy.

Target isoforms are an overlooked challenge and opportunity in chimeric antigen receptor cell therapy.

The development of novel chimeric antigen receptor (CAR) cell therapies is rapidly growing, with 299 new agents being reported and 109 new clinical trials initiated so far this year. One critical lesson from approved CD19-specific CAR therapies is that target isoform switching has been shown to cause tumour relapse, but little is known about the isoforms of CAR targets in solid cancers. Here we assess the protein isoform landscape and identify both the challenges and opportunities protein isoform switching present as CAR therapy is applied to solid cancers.

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CiteScore
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