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疟疾疫苗:当前成果与未来之路

Malaria Vaccines: Current Achievements and Path Forward.

作者信息

Chen Jiayan, Wang Qi, He Xiaomeng, Yang Bei

机构信息

Shanghai Institute for Advanced Immunochemical Studies and School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.

Shanghai Clinical Research and Trial Center, Shanghai 201210, China.

出版信息

Vaccines (Basel). 2025 May 19;13(5):542. doi: 10.3390/vaccines13050542.

DOI:10.3390/vaccines13050542
PMID:40432151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12115420/
Abstract

Malaria remains a significant global health challenge. Although the recent approval of the liver-stage vaccines RTS, S and R21 marks significant progress in malaria control, challenges remain in achieving long-lasting and broad protection. In this review, we provide an overview of the current landscape of malaria control, especially anti-malaria vaccine development. We first review the development of the RTS, S and R21 vaccines, highlighting their efficacy and limitations. We then examine other vaccines in development, including attenuated whole-sporozoite vaccines, as well as blood-stage-targeting vaccines and transmission-blocking vaccines targeting a variety of different immunogens. Additionally, we discuss emerging technologies, such as mRNA-based platforms, nanoparticle delivery systems, and novel adjuvants, assessing their potential to enhance the efficacy and mitigate the waning immunity concerns of most malaria vaccines. We believe that the identification of novel immunogen candidates, together with continued innovation in vaccine design and delivery, will enable us to win the fight against malaria in the future.

摘要

疟疾仍然是一项重大的全球卫生挑战。尽管近期肝期疫苗RTS、S和R21的获批标志着疟疾防控取得了重大进展,但在实现持久和广泛的保护方面仍存在挑战。在本综述中,我们概述了当前疟疾防控的现状,特别是抗疟疾疫苗的研发情况。我们首先回顾RTS、S和R21疫苗的研发过程,突出其疗效和局限性。然后,我们研究其他正在研发的疫苗,包括减毒全子孢子疫苗,以及针对不同免疫原的血期靶向疫苗和传播阻断疫苗。此外,我们还讨论了新兴技术,如基于mRNA的平台、纳米颗粒递送系统和新型佐剂,评估它们增强疗效和缓解大多数疟疾疫苗免疫衰退问题的潜力。我们相信,新型免疫原候选物的识别,以及疫苗设计和递送方面的持续创新,将使我们能够在未来战胜疟疾。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/ee364d5bd5ac/vaccines-13-00542-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/ab84e1334955/vaccines-13-00542-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/189686927828/vaccines-13-00542-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/4d7d070d7a11/vaccines-13-00542-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/ee364d5bd5ac/vaccines-13-00542-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/ab84e1334955/vaccines-13-00542-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/189686927828/vaccines-13-00542-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/4d7d070d7a11/vaccines-13-00542-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c5d/12115420/ee364d5bd5ac/vaccines-13-00542-g004.jpg

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本文引用的文献

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Malaria vaccines: a new era of prevention and control.疟疾疫苗:预防和控制的新时代。
Nat Rev Microbiol. 2024 Dec;22(12):756-772. doi: 10.1038/s41579-024-01065-7. Epub 2024 Jul 18.
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Blood-stage malaria vaccine candidate RH5.1/Matrix-M in healthy Tanzanian adults and children; an open-label, non-randomised, first-in-human, single-centre, phase 1b trial.健康坦桑尼亚成年人及儿童中血期疟疾候选疫苗RH5.1/Matrix-M;一项开放标签、非随机、人体首例、单中心1b期试验。
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A Pfs48/45-based vaccine to block Plasmodium falciparum transmission: phase 1, open-label, clinical trial.
一种基于Pfs48/45的阻断恶性疟原虫传播的疫苗:1期开放标签临床试验。
BMC Med. 2024 Apr 23;22(1):170. doi: 10.1186/s12916-024-03379-y.
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Safety and efficacy of malaria vaccine candidate R21/Matrix-M in African children: a multicentre, double-blind, randomised, phase 3 trial.疟疾疫苗候选物 R21/Matrix-M 在非洲儿童中的安全性和有效性:一项多中心、双盲、随机、3 期临床试验。
Lancet. 2024 Feb 10;403(10426):533-544. doi: 10.1016/S0140-6736(23)02511-4. Epub 2024 Feb 1.
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Malaria Vaccines: Progress to Date.疟疾疫苗:最新进展。
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Advancements and Challenges in Developing Malaria Vaccines: Targeting Multiple Stages of the Parasite Life Cycle.疟疾疫苗研发的进展与挑战:针对疟原虫生命周期的多个阶段
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Malaria transmission-blocking vaccines Pfs230D1-EPA and Pfs25-EPA in Alhydrogel in healthy Malian adults; a phase 1, randomised, controlled trial.在健康的马里成年人中用 Alhydrogel 佐剂的疟疾传播阻断疫苗 Pfs230D1-EPA 和 Pfs25-EPA:一项 1 期、随机、对照试验。
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The malaria blood stage antigen PfCyRPA formulated with the TLR-4 agonist adjuvant GLA-SE elicits parasite growth inhibitory antibodies in experimental animals.疟原虫血期抗原 PfCyRPA 与 TLR-4 激动剂佐剂 GLA-SE 联合使用,可在实验动物中诱导出抑制寄生虫生长的抗体。
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Fusion of the molecular adjuvant C3d to cleavage-independent native-like HIV-1 Env trimers improves the elicited antibody response.将分子佐剂 C3d 融合到无切割依赖性的天然样 HIV-1 Env 三聚体中可改善诱导的抗体反应。
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The Matrix-M™ adjuvant: A critical component of vaccines for the 21 century.Matrix-MTM 佐剂:21 世纪疫苗的关键组成部分。
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