Immunogenicity in CAR T cell immunotherapy

Yu Emily
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Abstract

Currently, the most accessible forms of cancer treatment include surgery, chemotherapy, and radiation. However, these forms of treatment may damage or destroy healthy tissue as well as cancerous cells, resulting in side effects such as fatigue, hair loss, diarrhea, etc. Immunotherapy, an alternative form of cancer treatment, is a growing treatment method of interest that uses bodily substances made by the body or in a laboratory to boost the immune system’s activity against tumor cells. One type of immunotherapy is CAR T cell therapy, in which a patient’s T cells are genetically modified in a lab to express Chimeric Antigen Receptors (CARs) that help T cells identify and destroy their target. However, because CARs are constructed in the lab and currently consist of non-self components, genetically engineered CAR T cells have the potential to induce anti-CAR immune responses. The following paper will explore the causes of anti-CAR immunity, its possible solutions, and the potential implications of these discoveries.
CAR - T细胞免疫治疗的免疫原性
目前,最容易获得的癌症治疗方式包括手术、化疗和放疗。然而,这些形式的治疗可能会损害或破坏健康组织以及癌细胞,导致副作用,如疲劳、脱发、腹泻等。免疫疗法是癌症治疗的另一种形式,是一种越来越受关注的治疗方法,它使用人体或实验室产生的物质来增强免疫系统对肿瘤细胞的活性。其中一种免疫疗法是CAR - T细胞疗法,在实验室中对患者的T细胞进行基因修饰,以表达嵌合抗原受体(CAR),帮助T细胞识别和摧毁它们的目标。然而,由于CAR - T细胞是在实验室中构建的,目前由非自身成分组成,基因工程CAR - T细胞有可能诱导抗CAR - T免疫反应。下面的文章将探讨抗car免疫的原因,其可能的解决方案,以及这些发现的潜在意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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