Developing cell-based therapies for pancreatic ductal adenocarcinoma.

Rachel Elizabeth Ann Fincham,Joe Poh Sheng Yeong,Hemant Mahendrakumar Kocher
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引用次数: 0

Abstract

Prostate stem cell antigen (PSCA) is highly and preferentially expressed on the surface of pancreatic ductal adenocarcinoma (PDAC) cells, raising the promise of tumor-selective cell-based immunotherapies. In this issue of the JCI, Dai et al. harness PSCA for the development of an off-the-shelf chimeric antigen receptor (CAR) invariant natural killer T (iNKT) cell-based treatment for PDAC. Through in vitro experiments and in vivo models, the authors demonstrate selectivity and therapeutic efficacy of PSCA CAR_sIL15 iNKT cells against both gemcitabine-sensitive and -resistant PDAC cells with comparable antitumor activity for freshly produced and frozen off-the-shelf PSCA CAR_sIL15 iNKT cells. This development opens another potential therapeutic option for pancreatic cancer.
发展胰腺导管腺癌的细胞疗法。
前列腺干细胞抗原(PSCA)在胰腺导管腺癌(PDAC)细胞表面高度优先表达,提高了肿瘤选择性细胞免疫治疗的前景。在这一期的JCI中,Dai等人利用PSCA开发了一种现成的嵌合抗原受体(CAR)不变自然杀伤T (iNKT)细胞治疗PDAC的方法。通过体外实验和体内模型,作者证明了PSCA CAR_sIL15 iNKT细胞对吉西他滨敏感和耐药的PDAC细胞的选择性和治疗效果,其抗肿瘤活性与新鲜生产和冷冻的现成PSCA CAR_sIL15 iNKT细胞相当。这一进展为胰腺癌开辟了另一种潜在的治疗选择。
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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