IA14:针对癌症独特体细胞突变的细胞转移免疫治疗

S. Rosenberg
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引用次数: 1

摘要

使用具有抗肿瘤活性的T淋巴细胞的过继细胞转移(ACT)免疫疗法是一种对各种转移性癌症患者非常有效的活疗法。自然发生的肿瘤浸润淋巴细胞(TIL)在体外扩大,并在淋巴细胞消耗预备方案后给予治疗,介导了194例患者中55%的转移性黑色素瘤的客观消退,其中24%的患者在3至10年后保持无病状态,完全消退。为了确定TIL识别的抗原,我们开发了一种基于癌症的深度外显子组测序和TIL或外周淋巴细胞的免疫学测试来产生识别免疫原性突变的t细胞的方法。来自22名转移性黑色素瘤患者的TIL识别出54个随机体细胞突变,其中没有一个在不同的黑色素瘤中共享。接下来,我们将这些研究扩展到常见上皮癌患者,结果显示,99例(82%)多种人类癌症类型(包括食管癌、结直肠癌、胆管癌、胃癌、胰腺癌、卵巢癌、宫颈癌和肺癌)患者中有81例(82%)含有识别197种新抗原的t细胞,除了KRAS(2例)外,所有这些新抗原都是独一无二的。针对独特的癌症突变已经扩展了ACT免疫治疗的范围,并被用于介导胆管、结肠癌、宫颈癌和乳腺癌化疗难治性转移癌患者的客观回归。除了使用自然发生的突变反应细胞外,我们还利用基因工程的自体淋巴细胞来表达共享的抗肿瘤T细胞受体(TCR)或嵌合抗原受体(CAR),用于ACT免疫治疗,可以介导重度预处理的难治性淋巴瘤、肉瘤和黑色素瘤患者的持久癌症消退。自体T细胞可以为难以接受常规癌症治疗的癌症患者提供高度个性化的免疫治疗。引文格式:Steven A. Rosenberg。针对癌症中独特体细胞突变的细胞转移免疫治疗[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要11 - 14。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract IA14: Cell transfer immunotherapy targeting unique somatic mutations in cancer
Adoptive cell transfer (ACT) immunotherapy using T lymphocytes with antitumor activity is a living therapy that can be highly effective in patients with a variety of metastatic cancers. Naturally occurring tumor infiltrating lymphocytes (TIL) expanded in vitro and administered following a lymphodepleting preparative regimen mediated objective regression of metastatic melanoma in 55% of 194 patients including complete regressions in 24% of patients who remain ongoing disease-free 3 to 10 years later. To determine the antigens recognized by TIL we developed an approach based on deep exomic sequencing of the cancer and immunologic testing of TIL or peripheral lymphocytes to generate T-cells that recognized immunogenic mutations. TIL from 22 patients with metastatic melanoma recognized 54 random somatic mutations none of which were shared among different melanomas. We next extended these studies to patients with common epithelial cancers and showed that 81 of 99 (82%) patients with a variety human cancer types including esophageal, colorectal, bile duct, gastric, pancreatic, ovarian, cervical and lung cancer contained T-cells that recognized 197 neoantigens all of which were unique except for KRAS (2 patients). Targeting unique cancer mutations has extended the reach of ACT immunotherapy and was used to mediate objective regressions in selected patients with chemorefractory metastatic cancers of the bile duct, colon, cervix, and breast. In addition to the use of naturally occurring mutation-reactive cells, we have genetically engineered autologous lymphocytes to express shared antitumor T- cell receptors (TCR) or chimeric antigen receptors (CAR) for use in ACT immunotherapy that can mediate durable cancer regressions in heavily pretreated patients with refractory lymphomas, sarcomas and melanoma. Autologous T- cells can be used to provide a highly personalized immunotherapy for cancer patients refractory to conventional cancer treatments. Citation Format: Steven A. Rosenberg. Cell transfer immunotherapy targeting unique somatic mutations in cancer [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr IA14.
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