• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

过继转移 T 细胞靶向的肿瘤新生抗原:不再是私人专属。

Cancer neoantigens targeted by adoptive T cell transfer: private no more.

机构信息

Laboratory of Translational Immunology and.

Flow Cytometry Core, Humanitas Clinical and Research Center, Rozzano, Milan, Italy.

出版信息

J Clin Invest. 2019 Mar 1;129(3):949-951. doi: 10.1172/JCI126295. Epub 2019 Feb 4.

DOI:10.1172/JCI126295
PMID:30714989
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6391111/
Abstract

Effector T cell responses directed toward cancer neoantigens mediate tumor regression following checkpoint blockade or adoptive T cell immunotherapy, but are generally "private", thus requiring considerable effort for their identification. In this issue of the JCI, Malekzadeh et al. show that a fraction of patients with epithelial cancers mount antigen-specific T cell responses to "hot spot" p53 mutations that in some cases are shared among patients. This work suggests that other genes frequently mutated in human cancer can be immunogenic, thus offering a rapid way to screen for cancer neoantigens that can be targeted by subsequent T cell-based therapies.

摘要

效应 T 细胞针对肿瘤新抗原的反应介导了检查点阻断或过继性 T 细胞免疫疗法后的肿瘤消退,但通常是“私人的”,因此需要相当大的努力来识别它们。在本期 JCI 中,Malekzadeh 等人表明,一部分上皮癌患者对“热点”p53 突变产生了抗原特异性 T 细胞反应,在某些情况下,这些突变在患者之间是共享的。这项工作表明,人类癌症中经常发生突变的其他基因也具有免疫原性,因此提供了一种快速筛选可被后续基于 T 细胞的治疗靶向的肿瘤新抗原的方法。

相似文献

1
Cancer neoantigens targeted by adoptive T cell transfer: private no more.过继转移 T 细胞靶向的肿瘤新生抗原:不再是私人专属。
J Clin Invest. 2019 Mar 1;129(3):949-951. doi: 10.1172/JCI126295. Epub 2019 Feb 4.
2
Using patient-derived tumor organoids from common epithelial cancers to analyze personalized T-cell responses to neoantigens.利用源自常见上皮癌的患者源性肿瘤类器官分析新抗原的个体化 T 细胞反应。
Cancer Immunol Immunother. 2023 Oct;72(10):3149-3162. doi: 10.1007/s00262-023-03476-6. Epub 2023 Jun 27.
3
Enhanced detection of neoantigen-reactive T cells targeting unique and shared oncogenes for personalized cancer immunotherapy.针对独特和共享致癌基因的新抗原反应性 T 细胞的增强检测,用于个性化癌症免疫治疗。
JCI Insight. 2018 Oct 4;3(19):122467. doi: 10.1172/jci.insight.122467.
4
Toward in silico Identification of Tumor Neoantigens in Immunotherapy.在免疫治疗中进行肿瘤新抗原的计算机识别。
Trends Mol Med. 2019 Nov;25(11):980-992. doi: 10.1016/j.molmed.2019.08.001. Epub 2019 Sep 4.
5
Landscape of immunogenic tumor antigens in successful immunotherapy of virally induced epithelial cancer.病毒诱导的上皮癌成功免疫治疗中免疫原性肿瘤抗原的格局
Science. 2017 Apr 14;356(6334):200-205. doi: 10.1126/science.aak9510.
6
Exploiting TCR Recognition of Shared Hotspot Oncogene-encoded Neoantigens.利用 TCR 识别共享热点致癌基因编码的新抗原。
Clin Cancer Res. 2020 Mar 15;26(6):1203-1204. doi: 10.1158/1078-0432.CCR-19-3813. Epub 2020 Jan 30.
7
Personalized T cell-mediated cancer immunotherapy: progress and challenges.个体化 T 细胞介导的癌症免疫治疗:进展与挑战。
Curr Opin Biotechnol. 2017 Dec;48:142-152. doi: 10.1016/j.copbio.2017.03.024. Epub 2017 May 8.
8
Immunologic Recognition of a Shared p53 Mutated Neoantigen in a Patient with Metastatic Colorectal Cancer.免疫识别转移性结直肠癌患者的共同 p53 突变新抗原。
Cancer Immunol Res. 2019 Apr;7(4):534-543. doi: 10.1158/2326-6066.CIR-18-0686. Epub 2019 Feb 1.
9
Adoptive T-Cell Therapy for Cancer.癌症的过继性T细胞疗法
Adv Immunol. 2016;130:279-94. doi: 10.1016/bs.ai.2015.12.006. Epub 2016 Feb 3.
10
Neoantigen-Specific T Cells in Adoptive Cell Therapy.过继细胞疗法中的新抗原特异性 T 细胞。
Cancer J. 2022;28(4):278-284. doi: 10.1097/PPO.0000000000000605.

引用本文的文献

1
Internal checkpoint regulates T cell neoantigen reactivity and susceptibility to PD1 blockade.内源性检查点调控 T 细胞新抗原反应性和对 PD-1 阻断的敏感性。
Med. 2022 Oct 14;3(10):682-704.e8. doi: 10.1016/j.medj.2022.07.008. Epub 2022 Aug 24.
2
Therapeutic Strategies Targeting Tumor Suppressor Genes in Pancreatic Cancer.胰腺癌中针对肿瘤抑制基因的治疗策略
Cancers (Basel). 2021 Aug 3;13(15):3920. doi: 10.3390/cancers13153920.

本文引用的文献

1
Neoantigen screening identifies broad TP53 mutant immunogenicity in patients with epithelial cancers.新抗原筛查确定了上皮癌患者中广泛的TP53突变免疫原性。
J Clin Invest. 2019 Mar 1;129(3):1109-1114. doi: 10.1172/JCI123791. Epub 2019 Feb 4.
2
Antioxidant metabolism regulates CD8+ T memory stem cell formation and antitumor immunity.抗氧化代谢调节 CD8+T 记忆干细胞的形成和抗肿瘤免疫。
JCI Insight. 2018 Sep 20;3(18). doi: 10.1172/jci.insight.122299.
3
High-dimensional single cell analysis identifies stem-like cytotoxic CD8 T cells infiltrating human tumors.高维单细胞分析鉴定出浸润人类肿瘤的类干细胞细胞毒性 CD8 T 细胞。
J Exp Med. 2018 Oct 1;215(10):2520-2535. doi: 10.1084/jem.20180684. Epub 2018 Aug 28.
4
Identification and Characterization of Neoantigens As Well As Respective Immune Responses in Cancer Patients.癌症患者中新抗原的鉴定与表征以及相应的免疫反应
Front Immunol. 2017 Nov 30;8:1702. doi: 10.3389/fimmu.2017.01702. eCollection 2017.
5
Targeting mutant p53 for efficient cancer therapy.针对突变型 p53 进行有效的癌症治疗。
Nat Rev Cancer. 2018 Feb;18(2):89-102. doi: 10.1038/nrc.2017.109. Epub 2017 Dec 15.
6
Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer.个体化 RNA 突变疫苗可动员针对癌症的多特异性治疗性免疫。
Nature. 2017 Jul 13;547(7662):222-226. doi: 10.1038/nature23003. Epub 2017 Jul 5.
7
Direct identification of clinically relevant neoepitopes presented on native human melanoma tissue by mass spectrometry.通过质谱直接鉴定天然人黑色素瘤组织上呈现的临床相关新表位。
Nat Commun. 2016 Nov 21;7:13404. doi: 10.1038/ncomms13404.
8
Targeting of cancer neoantigens with donor-derived T cell receptor repertoires.利用供体来源的 T 细胞受体库靶向癌症新生抗原。
Science. 2016 Jun 10;352(6291):1337-41. doi: 10.1126/science.aaf2288. Epub 2016 May 19.
9
PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.错配修复缺陷肿瘤中的程序性死亡受体-1阻断
N Engl J Med. 2015 Jun 25;372(26):2509-20. doi: 10.1056/NEJMoa1500596. Epub 2015 May 30.
10
Cooperativity of HIV-Specific Cytolytic CD4 T Cells and CD8 T Cells in Control of HIV Viremia.HIV特异性细胞溶解性CD4 T细胞与CD8 T细胞在控制HIV病毒血症中的协同作用。
J Virol. 2015 Aug;89(15):7494-505. doi: 10.1128/JVI.00438-15. Epub 2015 May 13.