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靶向血管生成的肽疫苗。

Targeting Angiogenesis With Peptide Vaccines.

机构信息

Immunotherapy Laboratory, Carmel Medical Center, Haifa, Israel.

The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.

出版信息

Front Immunol. 2019 Aug 8;10:1924. doi: 10.3389/fimmu.2019.01924. eCollection 2019.

DOI:10.3389/fimmu.2019.01924
PMID:31440262
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6694838/
Abstract

Most cancer peptide vaccinations tested so far are capable of eliciting a strong immune response, but demonstrate poor clinical benefits. Since peptide vaccination is safe and well-tolerated, and several indications suggest that it has clear potential advantages over other modalities of treatment, it is important to investigate the reasons for these clinical failures. In this review, the current state of the art in targeting angiogenic proteins via peptide vaccines is presented, and the underlying reasons for both the successes and the failures are analyzed. The review highlights a number of areas critical for future success, including choice of target antigens, types of peptides used, delivery methods and use of proper adjuvants, and suggests ways to achieve better clinical results in the future.

摘要

迄今为止,大多数经测试的癌症肽疫苗都能够引发强烈的免疫反应,但临床获益不佳。由于肽疫苗安全且耐受性良好,并且有几项适应证表明其比其他治疗方式具有明显优势,因此,研究这些临床失败的原因很重要。在本文中,介绍了通过肽疫苗靶向血管生成蛋白的最新技术现状,并分析了成功和失败的根本原因。本文重点介绍了一些未来成功的关键领域,包括靶抗原的选择、使用的肽类型、传递方法和适当佐剂的使用,并提出了未来实现更好临床效果的方法。

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Front Immunol. 2019 Aug 8;10:1924. doi: 10.3389/fimmu.2019.01924. eCollection 2019.
2
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本文引用的文献

1
Synergistic effect of immune checkpoint blockade and anti-angiogenesis in cancer treatment.免疫检查点阻断与抗血管生成在癌症治疗中的协同作用。
Mol Cancer. 2019 Mar 30;18(1):60. doi: 10.1186/s12943-019-0974-6.
2
Active Vaccination With EMMPRIN-Derived Multiple Antigenic Peptide (161-MAP) Reduces Angiogenesis in a Dextran Sodium Sulfate (DSS)-Induced Colitis Model.主动免疫 EMMPRIN 衍生的多种抗原肽(161-MAP)可减少葡聚糖硫酸钠(DSS)诱导的结肠炎模型中的血管生成。
Front Immunol. 2018 Dec 10;9:2919. doi: 10.3389/fimmu.2018.02919. eCollection 2018.
3
Trial watch: Peptide-based vaccines in anticancer therapy.试验观察:基于肽的疫苗在抗癌治疗中的应用
Oncoimmunology. 2018 Sep 6;7(12):e1511506. doi: 10.1080/2162402X.2018.1511506. eCollection 2018.
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Protein-based nanoparticles in cancer vaccine development.基于蛋白质的纳米颗粒在癌症疫苗开发中的应用。
Nanomedicine. 2019 Jan;15(1):164-174. doi: 10.1016/j.nano.2018.09.004. Epub 2018 Oct 4.
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The Latest Cancer Agents and Their Complications.最新的癌症治疗药物及其并发症。
Emerg Med Clin North Am. 2018 Aug;36(3):485-492. doi: 10.1016/j.emc.2018.04.006. Epub 2018 Jun 11.
6
Neoantigen Vaccine Delivery for Personalized Anticancer Immunotherapy.用于个性化抗癌免疫治疗的新抗原疫苗递送
Front Immunol. 2018 Jul 2;9:1499. doi: 10.3389/fimmu.2018.01499. eCollection 2018.
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A pilot study of peptide vaccines for VEGF receptor 1 and 2 in patients with recurrent/progressive high grade glioma.一项针对复发性/进展性高级别胶质瘤患者的VEGF受体1和2肽疫苗的初步研究。
Oncotarget. 2018 Apr 20;9(30):21569-21579. doi: 10.18632/oncotarget.25131.
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Update on Tumor Neoantigens and Their Utility: Why It Is Good to Be Different.肿瘤新抗原及其应用的最新进展:与众不同并非坏事。
Trends Immunol. 2018 Jul;39(7):536-548. doi: 10.1016/j.it.2018.04.005. Epub 2018 May 8.
9
Personalized cancer vaccines: adjuvants are important, too.个体化癌症疫苗:佐剂也很重要。
Cancer Immunol Immunother. 2018 Dec;67(12):1911-1918. doi: 10.1007/s00262-018-2158-4. Epub 2018 Apr 11.
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Peptide Vaccine Formulation Controls the Duration of Antigen Presentation and Magnitude of Tumor-Specific CD8 T Cell Response.肽疫苗配方控制抗原呈递的持续时间和肿瘤特异性 CD8 T 细胞反应的幅度。
J Immunol. 2018 May 15;200(10):3464-3474. doi: 10.4049/jimmunol.1700467. Epub 2018 Apr 11.