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Review of COVID-19 viral vector-based vaccines and COVID-19 variants.基于新冠病毒载体的疫苗及新冠病毒变异株综述。
Infez Med. 2021 Sep 10;29(3):328-338. doi: 10.53854/liim-2903-3. eCollection 2021.
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Review of the Current Landscape of the Potential of Nanotechnology for Future Malaria Diagnosis, Treatment, and Vaccination Strategies.纳米技术在未来疟疾诊断、治疗和疫苗接种策略中的潜力现状综述
Pharmaceutics. 2021 Dec 17;13(12):2189. doi: 10.3390/pharmaceutics13122189.
5
WHO gives first malaria vaccine the green light.世界卫生组织批准首款疟疾疫苗
Science. 2021 Oct 15;374(6565):245-246. doi: 10.1126/science.acx9344. Epub 2021 Oct 14.
6
Development and Delivery Systems of mRNA Vaccines.mRNA疫苗的开发与递送系统
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Efficacy of a low-dose candidate malaria vaccine, R21 in adjuvant Matrix-M, with seasonal administration to children in Burkina Faso: a randomised controlled trial.低剂量候选疟疾疫苗 R21 联合 Matrix-M 佐剂,季节性接种在布基纳法索儿童中的效果:一项随机对照试验。
Lancet. 2021 May 15;397(10287):1809-1818. doi: 10.1016/S0140-6736(21)00943-0. Epub 2021 May 5.
8
Self-amplifying mRNA-Based Vaccine Technology and Its Mode of Action.基于自我扩增信使 RNA 的疫苗技术及其作用模式。
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9
Nanotechnology approaches for global infectious diseases.纳米技术在全球传染病中的应用。
Nat Nanotechnol. 2021 Apr;16(4):369-384. doi: 10.1038/s41565-021-00866-8. Epub 2021 Mar 22.
10
Towards Eradication of Malaria: Is the WHO's RTS,S/AS01 Vaccination Effective Enough?迈向消除疟疾:世界卫生组织的RTS,S/AS01疫苗是否足够有效?
Risk Manag Healthc Policy. 2021 Mar 12;14:1033-1039. doi: 10.2147/RMHP.S219294. eCollection 2021.

对正在研发的疟疾疫苗候选物的全景综述。

A landscape review of malaria vaccine candidates in the pipeline.

作者信息

Tajudeen Yusuf Amuda, Oladipo Habeebullah Jayeola, Yusuff Sodiq Inaolaji, Abimbola Samuel O, Abdulkadir Muritala, Oladunjoye Iyiola Olatunji, Omotosho Abass Olawale, Egbewande Oluwaseyi Muyiwa, Shittu Hameedat Damilola, Yusuf Rashidat Onyinoyi, Ogundipe Oluwatosin, Muili Abdulbasit Opeyemi, Afolabi Abdullateef Opeyemi, Dahesh Salwa M A, Gameil Marwa Ahmed Mahmoud, El-Sherbini Mona Said

机构信息

Department of Microbiology, Faculty of Life Sciences, University of Ilorin, P.M.B. 1515, Ilorin, 240003, Nigeria.

Department of Epidemiology and Medical Statistics, Faculty of Public Health, College of Medicine, University of Ibadan, P.M.B 5017 G.P.O, Ibadan, Oyo State, Nigeria.

出版信息

Trop Dis Travel Med Vaccines. 2024 Aug 1;10(1):19. doi: 10.1186/s40794-024-00222-3.

DOI:10.1186/s40794-024-00222-3
PMID:39085983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11293096/
Abstract

BACKGROUND

Globally, malaria continues to pose a major health challenge, with approximately 247 million cases of the illness and 627,000 deaths reported in 2021. However, the threat is particularly pronounced in sub-Saharan African countries, where pregnant women and children under the age of five face heightened vulnerability to the disease. As a result, the imperative to develop malaria vaccines especially for these vulnerable populations, remains crucial in the pursuit of malaria eradication. However, despite decades of research, effective vaccine development faces technical challenges, including the rapid spread of drug-resistant parasite strains, the complex parasite lifecycle, the development of liver hypnozoites with potential for relapse, and evasion of the host immune system. This review aims to discuss the different malaria vaccine candidates in the pipeline, highlighting different approaches used for adjuvating these candidates, their benefits, and outcomes, and summarizing the progress of these vaccine candidates under development.

METHOD

A comprehensive web-based search for peer-reviewed journal articles published in SCOPUS, MEDLINE (via PubMed), Science Direct, WHO, and Advanced Google Scholar databases was conducted from 1990 to May 2022. Context-specific keywords such as "Malaria", "Malaria Vaccine", "Malaria Vaccine Candidates", "Vaccine Development", "Vaccine Safety", "Clinical Trials", "mRNA Vaccines", "Viral Vector Vaccines", "Protein-based Vaccines", "Subunit Vaccines", "Vaccine Adjuvants", "Vaccine-induced Immune Responses", and "Immunogenicity" were emphatically considered. Articles not directly related to malaria vaccine candidates in preclinical and clinical stages of development were excluded.

RESULTS

Various approaches have been studied for malaria vaccine development, targeting different parasite lifecycle stages, including the pre-erythrocytic, erythrocytic, and sexual stages. The RTS, S/AS01 vaccine, the first human parasite vaccine reaching WHO-listed authority maturity level 4, has demonstrated efficacy in preventing clinical malaria in African children. However, progress was slow in introducing other safe, and feasible malaria vaccines through clinical trials . Recent studies highlight the potential effectiveness of combining pre-erythrocytic and blood-stage vaccines, along with the advantages of mRNA vaccines for prophylaxis and treatment, and nonstructural vaccines for large-scale production.

CONCLUSION

Malaria vaccine candidates targeting different lifecycle stages of the parasite range from chemoprophylaxis vaccination to cross-species immune protection. The use of a multi-antigen, multi-stage combinational vaccine is therefore essential in the context of global health. This demands careful understanding and critical consideration of the long-term multi-faceted interplay of immune interference, co-dominance, complementary immune response, molecular targets, and adjuvants affecting the overall vaccine-induced immune response. Despite challenges, advancements in clinical trials and vaccination technology offer promising possibilities for novel approaches in malaria vaccine development.

摘要

背景

在全球范围内,疟疾仍然是一项重大的健康挑战,2021年报告了约2.47亿例疟疾病例和62.7万例死亡病例。然而,这种威胁在撒哈拉以南非洲国家尤为明显,在这些国家,孕妇和五岁以下儿童更容易感染这种疾病。因此,开发专门针对这些弱势群体的疟疾疫苗对于实现疟疾消除至关重要。然而,尽管经过了数十年的研究,有效的疫苗开发仍面临技术挑战,包括耐药寄生虫菌株的迅速传播、复杂的寄生虫生命周期、具有复发潜力的肝内休眠子的形成以及宿主免疫系统的逃避。本综述旨在讨论正在研发的不同疟疾疫苗候选物,强调用于佐剂化这些候选物的不同方法、它们的益处和结果,并总结这些正在研发的疫苗候选物的进展。

方法

从1990年至2022年5月,在SCOPUS、MEDLINE(通过PubMed)、Science Direct、世界卫生组织和高级谷歌学术数据库中对同行评审的期刊文章进行了全面的基于网络的搜索。特别考虑了特定背景的关键词,如“疟疾”、“疟疾疫苗”、“疟疾疫苗候选物”、“疫苗开发”、“疫苗安全性”、“临床试验”、“mRNA疫苗”、“病毒载体疫苗”、“基于蛋白质的疫苗”、“亚单位疫苗”、“疫苗佐剂”、“疫苗诱导的免疫反应”和“免疫原性”。排除了与处于临床前和临床开发阶段的疟疾疫苗候选物不直接相关的文章。

结果

针对疟疾疫苗开发已经研究了各种方法,针对不同的寄生虫生命周期阶段,包括前红细胞期、红细胞期和有性期。RTS,S/AS01疫苗是第一种达到世界卫生组织列出的权威成熟度4级的人类寄生虫疫苗,已证明在预防非洲儿童临床疟疾方面有效。然而,通过临床试验引入其他安全可行的疟疾疫苗进展缓慢。最近的研究强调了联合前红细胞期和血液期疫苗的潜在有效性,以及mRNA疫苗在预防和治疗方面的优势,以及非结构疫苗在大规模生产方面的优势。

结论

针对寄生虫不同生命周期阶段的疟疾疫苗候选物范围从化学预防疫苗到跨物种免疫保护。因此,在全球卫生背景下,使用多抗原、多阶段联合疫苗至关重要。这需要仔细理解和批判性考虑免疫干扰、共同主导、互补免疫反应、分子靶点和佐剂对整体疫苗诱导免疫反应的长期多方面相互作用。尽管存在挑战,但临床试验和疫苗接种技术的进步为疟疾疫苗开发的新方法提供了有希望的可能性。