• 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

相似文献

1
Progress towards the development of a vaccine.疫苗研发进展。
Expert Rev Vaccines. 2021 Feb;20(2):97-112. doi: 10.1080/14760584.2021.1880898. Epub 2021 Mar 4.
2
Potent immunogenicity of DNA vaccines encoding Plasmodium vivax transmission-blocking vaccine candidates Pvs25 and Pvs28-evaluation of homologous and heterologous antigen-delivery prime-boost strategy.编码间日疟原虫传播阻断疫苗候选抗原Pvs25和Pvs28的DNA疫苗的强免疫原性——同源和异源抗原递送初免-加强策略的评估
Vaccine. 2004 Aug 13;22(23-24):3205-13. doi: 10.1016/j.vaccine.2003.11.060.
3
From a basic to a functional approach for developing a blood stage vaccine against .从基础到功能方法开发针对 的红内期疫苗。
Expert Rev Vaccines. 2020 Feb;19(2):195-207. doi: 10.1080/14760584.2020.1733421. Epub 2020 Feb 28.
4
Platform for Plasmodium vivax vaccine discovery and development.疟原虫 vivax 疫苗发现和开发平台。
Mem Inst Oswaldo Cruz. 2011 Aug;106 Suppl 1(Suppl 1):179-92. doi: 10.1590/s0074-02762011000900023.
5
A Plasmodium vivax Plasmid DNA- and Adenovirus-Vectored Malaria Vaccine Encoding Blood-Stage Antigens AMA1 and MSP1 in a Prime/Boost Heterologous Immunization Regimen Partially Protects Aotus Monkeys against Blood-Stage Challenge.一种编码血液期抗原AMA1和MSP1的间日疟原虫质粒DNA和腺病毒载体疟疾疫苗,在初免/加强异源免疫方案中可部分保护夜猴免受血液期攻击。
Clin Vaccine Immunol. 2017 Apr 5;24(4). doi: 10.1128/CVI.00539-16. Print 2017 Apr.
6
Identification of an Immunogenic Broadly Inhibitory Surface Epitope of the Plasmodium vivax Duffy Binding Protein Ligand Domain.鉴定间日疟原虫红内期环子孢子蛋白配体结构域的一个免疫原性广谱抑制性表面表位。
mSphere. 2019 May 15;4(3):e00194-19. doi: 10.1128/mSphere.00194-19.
7
Tailoring a Plasmodium vivax Vaccine To Enhance Efficacy through a Combination of a CSP Virus-Like Particle and TRAP Viral Vectors.通过结合 CSP 病毒样颗粒和 TRAP 病毒载体来定制一种疟原虫疫苗以提高疗效。
Infect Immun. 2018 Aug 22;86(9). doi: 10.1128/IAI.00114-18. Print 2018 Sep.
8
The march toward malaria vaccines.迈向疟疾疫苗的征程。
Vaccine. 2015 Nov 27;33 Suppl 4(Suppl 4):D13-23. doi: 10.1016/j.vaccine.2015.07.091. Epub 2015 Aug 29.
9
A Multi-Stage Malaria Vaccine Candidate Able to Induce Long-Lived Antibody Responses Against Blood Stage Parasites and Robust Transmission-Blocking Activity.一种多阶段疟疾疫苗候选物,能够诱导针对红内期寄生虫的长期抗体应答,并具有强大的传播阻断活性。
Front Cell Infect Microbiol. 2019 May 1;9:135. doi: 10.3389/fcimb.2019.00135. eCollection 2019.
10
Transmission-Blocking Vaccines: Harnessing Herd Immunity for Malaria Elimination.阻断传播疫苗:利用群体免疫消除疟疾。
Expert Rev Vaccines. 2021 Feb;20(2):185-198. doi: 10.1080/14760584.2021.1878028. Epub 2021 Jan 31.

引用本文的文献

1
Malaria bivalent viral vectored vaccine protects against Plasmodium falciparum and vivax and blocks parasite transmission.疟疾双价病毒载体疫苗可预防恶性疟原虫和间日疟原虫,并阻断寄生虫传播。
NPJ Vaccines. 2025 Jul 26;10(1):171. doi: 10.1038/s41541-025-01229-3.
2
A novel micronemal protein MP38 is involved in the invasion of merozoites into erythrocytes.一种新型微线体蛋白MP38参与裂殖子侵入红细胞的过程。
mBio. 2025 May 14;16(5):e0391724. doi: 10.1128/mbio.03917-24. Epub 2025 Apr 9.
3
Atypical memory B cells from natural malaria infection produced broadly neutralizing antibodies against Plasmodium vivax variants.自然感染疟疾产生的非典型记忆B细胞产生了针对间日疟原虫变体的广泛中和抗体。
PLoS Pathog. 2025 Jan 23;21(1):e1012866. doi: 10.1371/journal.ppat.1012866. eCollection 2025 Jan.
4
The PvRBP2b-TfR1 interaction is not essential for reticulocytes invasion by Plasmodium vivax isolates from Cambodia.疟原虫结合蛋白2b(PvRBP2b)与转铁蛋白受体1(TfR1)的相互作用对于柬埔寨间日疟原虫分离株入侵网织红细胞并非必不可少。
NPJ Vaccines. 2024 Nov 22;9(1):232. doi: 10.1038/s41541-024-01031-7.
5
Natural genetic diversity of the DBL domain of a novel member of the Plasmodium vivax erythrocyte binding-like proteins (EBP2) in the Amazon rainforest.在亚马逊雨林中,新型恶性疟原虫红细胞结合蛋白样蛋白(EBP2)的 DBL 结构域的天然遗传多样性。
Infect Genet Evol. 2024 Sep;123:105628. doi: 10.1016/j.meegid.2024.105628. Epub 2024 Jun 25.
6
Evaluation of transmission-blocking potential of PvPSOP25 using transgenic murine malaria parasite and clinical isolates.利用转染的鼠疟寄生虫和临床分离株评估 PvPSOP25 的阻断传播潜能。
PLoS Negl Trop Dis. 2024 Jun 12;18(6):e0012231. doi: 10.1371/journal.pntd.0012231. eCollection 2024 Jun.
7
A two-dose viral-vectored multistage vaccine confers durable protection and transmission-blockade in a pre-clinical study.一项两剂病毒载体多阶段疫苗在临床前研究中提供了持久的保护和传播阻断。
Front Immunol. 2024 Apr 30;15:1372584. doi: 10.3389/fimmu.2024.1372584. eCollection 2024.
8
Naturally acquired antibodies against Plasmodium vivax pre-erythrocytic stage vaccine antigens inhibit sporozoite invasion of human hepatocytes in vitro.天然产生的针对间日疟原虫红细胞前期疫苗抗原的抗体可抑制疟原子在体外侵入人肝细胞。
Sci Rep. 2024 Jan 13;14(1):1260. doi: 10.1038/s41598-024-51820-2.
9
Sterile protection against malaria by repeated blood stage infection in the monkey model.经重复血期感染对猴子模型中的疟疾进行无菌保护。
Life Sci Alliance. 2023 Dec 29;7(3). doi: 10.26508/lsa.202302524. Print 2024 Mar.
10
Preliminary characterization of Plasmodium vivax sporozoite antigens as pre-erythrocytic vaccine candidates.初步鉴定间日疟原虫(Plasmodium vivax)子孢子抗原作为红细胞前期候选疫苗。
PLoS Negl Trop Dis. 2023 Sep 13;17(9):e0011598. doi: 10.1371/journal.pntd.0011598. eCollection 2023 Sep.

本文引用的文献

1
Malaria vaccines since 2000: progress, priorities, products.2000年以来的疟疾疫苗:进展、优先事项与产品
NPJ Vaccines. 2020 Jun 9;5(1):48. doi: 10.1038/s41541-020-0196-3. eCollection 2020.
2
A Multistage Formulation Based on Full-Length CSP and AMA-1 Ectodomain of Induces High Antibody Titers and T-cells and Partially Protects Mice Challenged with a Transgenic Parasite.基于全长CSP和AMA-1胞外结构域的多阶段配方诱导高抗体滴度和T细胞,并部分保护受到转基因寄生虫攻击的小鼠。
Microorganisms. 2020 Jun 17;8(6):916. doi: 10.3390/microorganisms8060916.
3
Development and validation of serological markers for detecting recent Plasmodium vivax infection.检测近期间日疟原虫感染的血清学标志物的开发和验证。
Nat Med. 2020 May;26(5):741-749. doi: 10.1038/s41591-020-0841-4. Epub 2020 May 11.
4
Protective efficacy of peptides from Plasmodium vivax circumsporozoite protein.疟原虫环子孢子蛋白肽的保护效力。
Vaccine. 2020 Jun 2;38(27):4346-4354. doi: 10.1016/j.vaccine.2020.03.063. Epub 2020 May 8.
5
Protective Immunity in Mice Immunized With MSP1-Based Formulations and Challenged With Expressing MSP1.用基于 MSP1 的制剂免疫小鼠并用表达 MSP1 的虫株进行攻毒,可诱导产生保护免疫。
Front Immunol. 2020 Feb 19;11:28. doi: 10.3389/fimmu.2020.00028. eCollection 2020.
6
The enigmatic mechanisms by which Plasmodium vivax infects Duffy-negative individuals.恶性疟原虫感染 Duffy 阴性个体的神秘机制。
PLoS Pathog. 2020 Feb 20;16(2):e1008258. doi: 10.1371/journal.ppat.1008258. eCollection 2020 Feb.
7
Amplification of Duffy binding protein-encoding gene allows Plasmodium vivax to evade host anti-DBP humoral immunity.Duffy 结合蛋白编码基因的扩增使间日疟原虫逃避宿主抗 DBP 体液免疫。
Nat Commun. 2020 Feb 19;11(1):953. doi: 10.1038/s41467-020-14574-9.
8
Antibody responses within two leading Plasmodium vivax vaccine candidate antigens in three geographically diverse malaria-endemic regions of India.在印度三个地理上不同的疟疾流行地区,两种主要的间日疟原虫候选疫苗抗原的抗体反应。
Malar J. 2019 Dec 16;18(1):425. doi: 10.1186/s12936-019-3066-6.
9
Naturally Acquired Antibody Response to Malaria Transmission Blocking Vaccine Candidate Pvs230 Domain 1.疟疾传播阻断候选疫苗 Pvs230 域 1 的天然抗体反应
Front Immunol. 2019 Oct 4;10:2295. doi: 10.3389/fimmu.2019.02295. eCollection 2019.
10
Plasmodium vivax Reticulocyte Binding Proteins for invasion into reticulocytes.恶性疟原虫 (Plasmodium vivax) 红细胞内期入侵相关的结合蛋白。
Cell Microbiol. 2020 Jan;22(1):e13110. doi: 10.1111/cmi.13110. Epub 2019 Sep 8.

疫苗研发进展。

Progress towards the development of a vaccine.

机构信息

Center for Global Health and Infectious Diseases Research, College of Public Health, University of South Florida, Tampa, FL, USA.

出版信息

Expert Rev Vaccines. 2021 Feb;20(2):97-112. doi: 10.1080/14760584.2021.1880898. Epub 2021 Mar 4.

DOI:10.1080/14760584.2021.1880898
PMID:33481638
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7994195/
Abstract

INTRODUCTION

causes significant public health problems in endemic regions. A vaccine to prevent disease is critical, considering the rapid spread of drug-resistant parasite strains, and the development of hypnozoites in the liver with potential for relapse. A minimally effective vaccine should prevent disease and transmission while an ideal vaccine provides sterile immunity.

AREAS COVERED

Despite decades of research, the complex life cycle, technical challenges and a lack of funding have hampered progress of vaccine development. Here, we review the progress of potential vaccine candidates from different stages of the parasite life cycle. We also highlight the challenges and important strategies for rational vaccine design. These factors can significantly increase immune effector mechanisms and improve the protective efficacy of these candidates in clinical trials to generate sustained protection over longer periods of time.

EXPERT OPINION

A vaccine that presents functionally-conserved epitopes from multiple antigens from various stages of the parasite life cycle is key to induce broadly neutralizing strain-transcending protective immunity to effectively disrupt parasite development and transmission.

摘要

简介

在流行地区,疟疾会引发严重的公共卫生问题。考虑到耐药性寄生虫株的快速传播,以及肝脏中休眠疟原虫的潜在复发,预防疾病的疫苗至关重要。一种最低限度有效的疫苗应该可以预防疾病和传播,而理想的疫苗则提供无菌免疫。

涵盖领域

尽管经过了几十年的研究,但复杂的生命周期、技术挑战以及资金短缺都阻碍了疫苗开发的进展。在这里,我们回顾了寄生虫生命周期不同阶段的潜在疫苗候选物的进展。我们还强调了合理疫苗设计的挑战和重要策略。这些因素可以显著增加免疫效应机制,并提高这些候选物在临床试验中的保护效果,从而在更长时间内产生持续保护。

专家意见

一种疫苗,如果能呈现来自寄生虫生命周期各个阶段的多种抗原的功能保守表位,是诱导广泛中和、具有跨越株保护作用的免疫的关键,从而有效破坏寄生虫的发育和传播。