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EGFRvIII mCAR-modified T-cell therapy cures mice with established intracerebral glioma and generates host immunity against tumor-antigen loss

机译:EGFRvIII mCAR修饰的T细胞疗法可治愈已建立的脑内神经胶质瘤的小鼠并产生抗肿瘤抗原损失的宿主免疫力

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摘要

PurposeChimeric antigen receptor (CAR) transduced T cells represent a promising immune therapy that has been shown to successfully treat cancers in mice and humans. However, CARs targeting antigens expressed in both tumors and normal tissues have led to significant toxicity. Preclinical studies have been limited by the use of xenograft models that do not adequately recapitulate the immune system of a clinically relevant host. EGFRvIII is a constitutively activated mutant of the naturally occurring epidermal growth factor receptor and is antigenically identical in both human and mouse glioma, but is also completely absent from any normal tissues.
机译:目的嵌合抗原受体(CAR)转导的T细胞代表着一种有前途的免疫疗法,已被证明可以成功治疗小鼠和人类的癌症。然而,靶向肿瘤和正常组织中表达的抗原的CARs已导致明显的毒性。临床前研究受到使用不能充分概括临床相关宿主免疫系统的异种移植模型的限制。 EGFRvIII是天然存在的表皮生长因子受体的组成型激活突变体,在人和小鼠神经胶质瘤中在抗原上相同,但在任何正常组织中都不存在。

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