• 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

增强抗癌疫苗:好事过头了?

Boosting anticancer vaccines: Too much of a good thing?

作者信息

Ricupito Alessia, Grioni Matteo, Calcinotto Arianna, Bellone Matteo

机构信息

Cellular Immunology Unit; San Raffaele Scientific Institute; Milan, Italy.

出版信息

Oncoimmunology. 2013 Jul 1;2(7):e25032. doi: 10.4161/onci.25032. Epub 2013 May 16.

DOI:10.4161/onci.25032
PMID:24073378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3782130/
Abstract

Using both transplantable and oncogene-driven autochthonous tumor models challenged with dendritic cell-based vaccines, we have recently found that boosting provides a clear advantage in prophylactic settings, unless performed on an excessively tight schedule, which causes the loss of central memory T cells. In therapeutic settings, boosting turned out to be always detrimental.

摘要

使用可移植和癌基因驱动的原位肿瘤模型,并以基于树突状细胞的疫苗进行挑战,我们最近发现,在预防性环境中,加强免疫提供了明显的优势,除非在过于紧凑的时间表上进行,这会导致中央记忆T细胞的损失。在治疗性环境中,加强免疫结果总是有害的。

相似文献

1
Boosting anticancer vaccines: Too much of a good thing?增强抗癌疫苗:好事过头了?
Oncoimmunology. 2013 Jul 1;2(7):e25032. doi: 10.4161/onci.25032. Epub 2013 May 16.
2
Booster vaccinations against cancer are critical in prophylactic but detrimental in therapeutic settings.癌症的加强型疫苗接种在预防方面至关重要,但在治疗方面却有害无益。
Cancer Res. 2013 Jun 15;73(12):3545-54. doi: 10.1158/0008-5472.CAN-12-2449. Epub 2013 Mar 28.
3
Hyperthermic treatment at 56 °C induces tumour-specific immune protection in a mouse model of prostate cancer in both prophylactic and therapeutic immunization regimens.56°C 的热疗在前列腺癌的小鼠模型中诱导了肿瘤特异性免疫保护,无论是在预防性还是治疗性免疫接种方案中。
Vaccine. 2018 Jun 14;36(25):3708-3716. doi: 10.1016/j.vaccine.2018.05.010. Epub 2018 May 8.
4
Lentivector prime and vaccinia virus vector boost generate high-quality CD8 memory T cells and prevent autochthonous mouse melanoma.慢病毒载体疫苗和痘苗病毒载体加强可产生高质量的 CD8 记忆 T 细胞,并预防自发的小鼠黑色素瘤。
J Immunol. 2011 Aug 15;187(4):1788-96. doi: 10.4049/jimmunol.1101138. Epub 2011 Jul 11.
5
Type I-polarized BRAF-pulsed dendritic cells induce antigen-specific CD8+ T cells that impact BRAF-mutant murine melanoma.I型极化的BRAF脉冲树突状细胞诱导抗原特异性CD8 + T细胞,这些细胞会影响BRAF突变的小鼠黑色素瘤。
Melanoma Res. 2016 Feb;26(1):1-11. doi: 10.1097/CMR.0000000000000203.
6
Versatile prostate cancer treatment with inducible caspase and interleukin-12.采用可诱导半胱天冬酶和白细胞介素-12的多功能前列腺癌治疗方法。
Cancer Res. 2005 May 15;65(10):4309-19. doi: 10.1158/0008-5472.CAN-04-3119.
7
[Ad hTRP2 - mediated immunity against melanoma is enhanced by dendritic cells pulsed with peptide].[用肽脉冲处理的树突状细胞增强了抗黑素瘤的腺病毒介导免疫]
Zhonghua Zhong Liu Za Zhi. 2006 Sep;28(9):658-61.
8
Tumor vaccines expressing flt3 ligand synergize with ctla-4 blockade to reject preimplanted tumors.表达Flt3配体的肿瘤疫苗与CTLA-4阻断协同作用以排斥植入前的肿瘤。
Cancer Res. 2009 Oct 1;69(19):7747-55. doi: 10.1158/0008-5472.CAN-08-3289. Epub 2009 Sep 8.
9
Enhancing efficacy of recombinant anticancer vaccines with prime/boost regimens that use two different vectors.通过使用两种不同载体的初免/加强免疫方案提高重组抗癌疫苗的疗效。
J Natl Cancer Inst. 1997 Nov 5;89(21):1595-601. doi: 10.1093/jnci/89.21.1595.
10
Boosting vaccinations with peptide-pulsed CD34+ progenitor-derived dendritic cells can expand long-lived melanoma peptide-specific CD8+ T cells in patients with metastatic melanoma.用肽脉冲的CD34 +祖细胞衍生的树突状细胞加强疫苗接种可在转移性黑色素瘤患者中扩增长寿的黑色素瘤肽特异性CD8 + T细胞。
J Immunother. 2005 Mar-Apr;28(2):158-68. doi: 10.1097/01.cji.0000154249.74383.17.

引用本文的文献

1
Recent Advances in Cancer Vaccines: Challenges, Achievements, and Futuristic Prospects.癌症疫苗的最新进展:挑战、成就与未来前景
Vaccines (Basel). 2022 Nov 25;10(12):2011. doi: 10.3390/vaccines10122011.
2
Trial watch: Naked and vectored DNA-based anticancer vaccines.试验观察:裸 DNA 与载体 DNA 抗癌疫苗。
Oncoimmunology. 2015 Apr 2;4(5):e1026531. doi: 10.1080/2162402X.2015.1026531. eCollection 2015 May.
3
Trial Watch: Peptide-based anticancer vaccines.试验观察:基于肽的抗癌疫苗

本文引用的文献

1
Booster vaccinations against cancer are critical in prophylactic but detrimental in therapeutic settings.癌症的加强型疫苗接种在预防方面至关重要,但在治疗方面却有害无益。
Cancer Res. 2013 Jun 15;73(12):3545-54. doi: 10.1158/0008-5472.CAN-12-2449. Epub 2013 Mar 28.
2
Persistent antigen at vaccination sites induces tumor-specific CD8⁺ T cell sequestration, dysfunction and deletion.疫苗接种部位持续存在的抗原诱导肿瘤特异性 CD8+T 细胞隔离、功能障碍和缺失。
Nat Med. 2013 Apr;19(4):465-72. doi: 10.1038/nm.3105. Epub 2013 Mar 3.
3
From vaccines to memory and back.
Oncoimmunology. 2015 Jan 9;4(4):e974411. doi: 10.4161/2162402X.2014.974411. eCollection 2015 Apr.
4
Classification of current anticancer immunotherapies.当前抗癌免疫疗法的分类。
Oncotarget. 2014 Dec 30;5(24):12472-508. doi: 10.18632/oncotarget.2998.
5
Dendritic cell-based approaches in the fight against diseases.基于树突状细胞的疾病防治方法。
Front Immunol. 2014 Feb 26;5:78. doi: 10.3389/fimmu.2014.00078. eCollection 2014.
从疫苗到记忆,再回到疫苗。
Immunity. 2010 Oct 29;33(4):451-63. doi: 10.1016/j.immuni.2010.10.008.
4
Partial CD4 depletion reduces regulatory T cells induced by multiple vaccinations and restores therapeutic efficacy.部分 CD4 细胞耗竭可减少多次疫苗接种诱导的调节性 T 细胞,并恢复治疗效果。
Clin Cancer Res. 2009 Nov 15;15(22):6881-90. doi: 10.1158/1078-0432.CCR-09-1113. Epub 2009 Nov 10.
5
CD8+ T-cell memory in tumor immunology and immunotherapy.肿瘤免疫学与免疫治疗中的CD8 + T细胞记忆
Immunol Rev. 2006 Jun;211:214-24. doi: 10.1111/j.0105-2896.2006.00391.x.
6
Mature dendritic cells boost functionally superior CD8(+) T-cell in humans without foreign helper epitopes.成熟树突状细胞在无外来辅助表位的情况下增强人体中功能更优的CD8(+) T细胞。
J Clin Invest. 2000 Mar;105(6):R9-R14. doi: 10.1172/JCI9051.
7
Two subsets of memory T lymphocytes with distinct homing potentials and effector functions.具有不同归巢潜能和效应功能的记忆性T淋巴细胞的两个亚群。
Nature. 1999 Oct 14;401(6754):708-12. doi: 10.1038/44385.