• 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

抗癌疫苗接种中的树突状细胞:体外负载或体内靶向的原理

Dendritic Cells in Anticancer Vaccination: Rationale for Ex Vivo Loading or In Vivo Targeting.

作者信息

Baldin Alexey V, Savvateeva Lyudmila V, Bazhin Alexandr V, Zamyatnin Andrey A

机构信息

Institute of Molecular Medicine, Sechenov First Moscow State Medical University, 119991 Moscow, Russia.

Department of General, Visceral and Transplant Surgery, Ludwig-Maximilians University of Munich, 81377 Munich, Germany.

出版信息

Cancers (Basel). 2020 Mar 5;12(3):590. doi: 10.3390/cancers12030590.

DOI:10.3390/cancers12030590
PMID:32150821
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7139354/
Abstract

Dendritic cells (DCs) have shown great potential as a component or target in the landscape of cancer immunotherapy. Different in vivo and ex vivo strategies of DC vaccine generation with different outcomes have been proposed. Numerous clinical trials have demonstrated their efficacy and safety in cancer patients. However, there is no consensus regarding which DC-based vaccine generation method is preferable. A problem of result comparison between trials in which different DC-loading or -targeting approaches have been applied remains. The employment of different DC generation and maturation methods, antigens and administration routes from trial to trial also limits the objective comparison of DC vaccines. In the present review, we discuss different methods of DC vaccine generation. We conclude that standardized trial designs, treatment settings and outcome assessment criteria will help to determine which DC vaccine generation approach should be applied in certain cancer cases. This will result in a reduction in alternatives in the selection of preferable DC-based vaccine tactics in patient. Moreover, it has become clear that the application of a DC vaccine alone is not sufficient and combination immunotherapy with recent advances, such as immune checkpoint inhibitors, should be employed to achieve a better clinical response and outcome.

摘要

树突状细胞(DC)在癌症免疫治疗领域作为一种组成部分或靶点已展现出巨大潜力。人们提出了不同的体内和体外生成DC疫苗的策略,其结果各异。众多临床试验已证明它们在癌症患者中的有效性和安全性。然而,对于哪种基于DC的疫苗生成方法更优尚无共识。在应用了不同DC负载或靶向方法的试验之间,结果比较存在问题。每次试验中使用不同的DC生成和成熟方法、抗原及给药途径,也限制了DC疫苗的客观比较。在本综述中,我们讨论了DC疫苗生成的不同方法。我们得出结论,标准化的试验设计、治疗设置和结果评估标准将有助于确定在某些癌症病例中应采用哪种DC疫苗生成方法。这将减少患者在选择更优的基于DC的疫苗策略时的备选方案。此外,已明确仅应用DC疫苗是不够的,应采用与免疫检查点抑制剂等最新进展相结合的联合免疫疗法,以实现更好的临床反应和结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/280c8d8297f4/cancers-12-00590-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/0762d4b72c86/cancers-12-00590-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/08a5e4089172/cancers-12-00590-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/280c8d8297f4/cancers-12-00590-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/0762d4b72c86/cancers-12-00590-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/08a5e4089172/cancers-12-00590-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cf4/7139354/280c8d8297f4/cancers-12-00590-g003.jpg

相似文献

1
Dendritic Cells in Anticancer Vaccination: Rationale for Ex Vivo Loading or In Vivo Targeting.抗癌疫苗接种中的树突状细胞:体外负载或体内靶向的原理
Cancers (Basel). 2020 Mar 5;12(3):590. doi: 10.3390/cancers12030590.
2
Assessment of Immune Response Following Dendritic Cell-Based Immunotherapy in Pediatric Patients With Relapsing Sarcoma.复发肉瘤儿科患者基于树突状细胞免疫疗法后的免疫反应评估
Front Oncol. 2019 Nov 14;9:1169. doi: 10.3389/fonc.2019.01169. eCollection 2019.
3
Therapeutic dendritic cell-based cancer vaccines: the state of the art.基于治疗性树突状细胞的癌症疫苗:现状
Crit Rev Immunol. 2013;33(6):489-547. doi: 10.1615/critrevimmunol.2013008033.
4
Dendritic cell based vaccines: progress in immunotherapy studies for prostate cancer.基于树突状细胞的疫苗:前列腺癌免疫治疗研究进展
J Urol. 2004 Dec;172(6 Pt 2):2532-8. doi: 10.1097/01.ju.0000144211.51111.e4.
5
Dendritic cell gene therapy.树突状细胞基因治疗。
Surg Oncol Clin N Am. 2002 Jul;11(3):645-60. doi: 10.1016/s1055-3207(02)00027-3.
6
IFN-Alpha-Mediated Differentiation of Dendritic Cells for Cancer Immunotherapy: Advances and Perspectives.干扰素-α介导的树突状细胞分化用于癌症免疫治疗:进展与展望
Vaccines (Basel). 2020 Oct 19;8(4):617. doi: 10.3390/vaccines8040617.
7
Trial watch: Dendritic cell-based anticancer immunotherapy.试验观察:基于树突状细胞的抗癌免疫疗法。
Oncoimmunology. 2017 May 12;6(7):e1328341. doi: 10.1080/2162402X.2017.1328341. eCollection 2017.
8
Trial watch: dendritic cell vaccination for cancer immunotherapy.试验观察:用于癌症免疫治疗的树突状细胞疫苗接种
Oncoimmunology. 2019 Jul 18;8(11):e1638212. doi: 10.1080/2162402X.2019.1638212. eCollection 2019.
9
A Phase I/II trial comparing autologous dendritic cell vaccine pulsed either with personalized peptides (PEP-DC) or with tumor lysate (OC-DC) in patients with advanced high-grade ovarian serous carcinoma.一项Ⅰ/Ⅱ期临床试验,比较了自体树突状细胞疫苗(PEP-DC)或肿瘤裂解物(OC-DC)脉冲加载个体化肽在晚期高级别卵巢浆液性癌患者中的疗效。
J Transl Med. 2019 Nov 26;17(1):391. doi: 10.1186/s12967-019-02133-w.
10
Optimizing dendritic cell-based approaches for cancer immunotherapy.优化基于树突状细胞的癌症免疫治疗方法。
Yale J Biol Med. 2014 Dec 12;87(4):491-518. eCollection 2014 Dec.

引用本文的文献

1
Intradermally Administered Retinoic Acid or Vitamin D3-Loaded Liposomes Induce Tolerogenic Skin Dendritic Cells.皮内注射维甲酸或负载维生素D3的脂质体可诱导具有耐受性的皮肤树突状细胞。
J Immunol Res. 2025 Aug 4;2025:2208155. doi: 10.1155/jimr/2208155. eCollection 2025.
2
Immunotherapy in Glioblastoma: An Overview of Current Status.胶质母细胞瘤的免疫治疗:现状概述
Clin Pharmacol. 2025 Jul 24;17:185-209. doi: 10.2147/CPAA.S497903. eCollection 2025.
3
Immuno-Oncology at the Crossroads: Confronting Challenges in the Quest for Effective Cancer Therapies.

本文引用的文献

1
Trial watch: dendritic cell vaccination for cancer immunotherapy.试验观察:用于癌症免疫治疗的树突状细胞疫苗接种
Oncoimmunology. 2019 Jul 18;8(11):e1638212. doi: 10.1080/2162402X.2019.1638212. eCollection 2019.
2
Current Perspectives in Cancer Immunotherapy.癌症免疫疗法的当前观点
Cancers (Basel). 2019 Sep 30;11(10):1472. doi: 10.3390/cancers11101472.
3
Tumor neoantigens: from basic research to clinical applications.肿瘤新生抗原:从基础研究到临床应用。
免疫肿瘤学处于十字路口:在寻求有效癌症疗法的过程中面临挑战。
Int J Mol Sci. 2025 Jun 26;26(13):6177. doi: 10.3390/ijms26136177.
4
Dendritic Cell-Based Cancer Vaccines: The Impact of Modulating Innate Lymphoid Cells on Anti-Tumor Efficacy.基于树突状细胞的癌症疫苗:调节固有淋巴细胞对抗肿瘤疗效的影响
Cells. 2025 May 30;14(11):812. doi: 10.3390/cells14110812.
5
Tug of war: Understanding the dynamic interplay of tumor biomechanical environment on dendritic cell function.拔河:理解肿瘤生物力学环境对树突状细胞功能的动态相互作用。
Mechanobiol Med. 2024 Apr 27;2(3):100068. doi: 10.1016/j.mbm.2024.100068. eCollection 2024 Sep.
6
Promising Cellular Immunotherapy for Colorectal Cancer Using Classical Dendritic Cells and Natural Killer T Cells.使用经典树突状细胞和自然杀伤T细胞对结直肠癌进行有前景的细胞免疫治疗。
Cells. 2025 Jan 22;14(3):166. doi: 10.3390/cells14030166.
7
Harnessing the tumor microenvironment: targeted cancer therapies through modulation of epithelial-mesenchymal transition.利用肿瘤微环境:通过调节上皮-间质转化实现靶向癌症治疗
J Hematol Oncol. 2025 Jan 13;18(1):6. doi: 10.1186/s13045-024-01634-6.
8
Nanobodies Outperform Antibodies - Rapid Functionalization with Equal In Vivo Targeting Properties.纳米抗体优于抗体——具有同等体内靶向特性的快速功能化。
Adv Mater. 2024 Dec;36(52):e2412563. doi: 10.1002/adma.202412563. Epub 2024 Oct 29.
9
Immunotherapy for Treatment of Pleural Mesothelioma: Current and Emerging Therapeutic Strategies.胸膜间皮瘤的免疫治疗:当前和新兴的治疗策略。
Int J Mol Sci. 2024 Oct 9;25(19):10861. doi: 10.3390/ijms251910861.
10
The clinical impact of mRNA therapeutics in the treatment of cancers, infections, genetic disorders, and autoimmune diseases.信使核糖核酸(mRNA)疗法在癌症、感染性疾病、遗传性疾病和自身免疫性疾病治疗中的临床影响。
Heliyon. 2024 Feb 29;10(5):e26971. doi: 10.1016/j.heliyon.2024.e26971. eCollection 2024 Mar 15.
J Hematol Oncol. 2019 Sep 6;12(1):93. doi: 10.1186/s13045-019-0787-5.
4
Best practices for bioinformatic characterization of neoantigens for clinical utility.用于临床应用的新抗原生物信息学特征描述的最佳实践。
Genome Med. 2019 Aug 28;11(1):56. doi: 10.1186/s13073-019-0666-2.
5
Supplementary granulocyte macrophage colony-stimulating factor to chemotherapy and programmed death-ligand 1 blockade decreases local recurrence after surgery in bladder cancer.化疗联合程序性死亡配体 1 阻断及辅助粒细胞巨噬细胞集落刺激因子治疗降低膀胱癌术后局部复发率。
Cancer Sci. 2019 Oct;110(10):3315-3327. doi: 10.1111/cas.14158. Epub 2019 Aug 19.
6
The STING activator c-di-AMP exerts superior adjuvant properties than the formulation poly(I:C)/CpG after subcutaneous vaccination with soluble protein antigen or DEC-205-mediated antigen targeting to dendritic cells.STING 激活剂 c-di-AMP 比制剂 poly(I:C)/CpG 在皮下接种可溶性蛋白抗原或 DEC-205 介导的树突状细胞靶向抗原后具有更好的佐剂特性。
Vaccine. 2019 Aug 14;37(35):4963-4974. doi: 10.1016/j.vaccine.2019.07.019. Epub 2019 Jul 15.
7
Antigen structure affects cellular routing through DC-SIGN.抗原结构通过 DC-SIGN 影响细胞途径。
Proc Natl Acad Sci U S A. 2019 Jul 23;116(30):14862-14867. doi: 10.1073/pnas.1820165116. Epub 2019 Jul 3.
8
Advancing immunomodulation by in vivo antigen delivery to DEC-205 and other cell surface molecules using recombinant chimeric antibodies.利用重组嵌合抗体通过体内抗原递送至 DEC-205 和其他细胞表面分子来推进免疫调节。
Int Immunopharmacol. 2019 Aug;73:575-580. doi: 10.1016/j.intimp.2019.05.037. Epub 2019 Jun 19.
9
First-in-Class, First-in-Human Study Evaluating LV305, a Dendritic-Cell Tropic Lentiviral Vector, in Sarcoma and Other Solid Tumors Expressing NY-ESO-1.评估表达 NY-ESO-1 的肉瘤和其他实体瘤中树突状细胞嗜性慢病毒载体 LV305 的首例人体研究。
Clin Cancer Res. 2019 Oct 1;25(19):5808-5817. doi: 10.1158/1078-0432.CCR-19-1025. Epub 2019 Jun 21.
10
Human Dendritic Cell Subsets, Ontogeny, and Impact on HIV Infection.人类树突状细胞亚群、发生和对 HIV 感染的影响。
Front Immunol. 2019 May 16;10:1088. doi: 10.3389/fimmu.2019.01088. eCollection 2019.