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优化用于结核病疫苗研发的抗原选择。

Optimizing antigen selection for the development of tuberculosis vaccines.

作者信息

Yang Yang, Chen Yi-Zhen, Xia Tian

机构信息

State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.

Gansu Province Research Center for Basic Disciplines of Pathogen Biology, Lanzhou, 730046, China.

出版信息

Cell Insight. 2024 Mar 16;3(3):100163. doi: 10.1016/j.cellin.2024.100163. eCollection 2024 Jun.

Abstract

Tuberculosis (TB) remains a prevalent global infectious disease caused by genetically closely related tubercle bacilli in complex (MTBC). For a century, the Bacillus Calmette-Guérin (BCG) vaccine has been the primary preventive measure against TB. While it effectively protects against extrapulmonary forms of pediatric TB, it lacks consistent efficacy in providing protection against pulmonary TB in adults. Consequently, the exploration and development of novel TB vaccines, capable of providing broad protection to populations, have consistently constituted a prominent area of interest in medical research. This article presents a concise overview of the novel TB vaccines currently undergoing clinical trials, discussing their classification, protective efficacy, immunogenicity, advantages, and limitations. In vaccine development, the careful selection of antigens that can induce strong and diverse specific immune responses is essential. Therefore, we have summarized the molecular characteristics, biological function, immunogenicity, and relevant studies associated with the chosen antigens for TB vaccines. These insights gained from vaccines and immunogenic proteins will inform the development of novel mycobacterial vaccines, particularly mRNA vaccines, for effective TB control.

摘要

结核病(TB)仍然是一种全球流行的传染病,由基因密切相关的结核杆菌复合群(MTBC)引起。一个世纪以来,卡介苗(BCG)一直是预防结核病的主要措施。虽然它能有效预防儿童肺外结核病,但在预防成人肺结核方面缺乏一致的疗效。因此,开发能够为人群提供广泛保护的新型结核病疫苗一直是医学研究中一个备受关注的重要领域。本文简要概述了目前正在进行临床试验的新型结核病疫苗,讨论了它们的分类、保护效力、免疫原性、优点和局限性。在疫苗研发中,精心选择能够诱导强烈且多样的特异性免疫反应的抗原至关重要。因此,我们总结了与所选结核病疫苗抗原相关的分子特征、生物学功能、免疫原性及相关研究。从疫苗和免疫原性蛋白中获得的这些见解将为开发新型分枝杆菌疫苗,特别是mRNA疫苗,以有效控制结核病提供参考。

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本文引用的文献

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4
Immunogenicity and efficacy analyses of EPC002, ECA006, and EPCP009 protein subunit combinations as tuberculosis vaccine candidates.
Vaccine. 2023 Jun 13;41(26):3836-3846. doi: 10.1016/j.vaccine.2023.04.003. Epub 2023 May 22.
5
Emerging SARS-CoV-2 variants: Why, how, and what's next?
Cell Insight. 2022 May 2;1(3):100029. doi: 10.1016/j.cellin.2022.100029. eCollection 2022 Jun.
6
Single-cell transcriptomic landscape identifies the expansion of peripheral blood monocytes as an indicator of HIV-1-TB co-infection.
Cell Insight. 2022 Jan 21;1(1):100005. doi: 10.1016/j.cellin.2022.100005. eCollection 2022 Feb.
7
mRNA vaccines: a new opportunity for malaria, tuberculosis and HIV.
Front Immunol. 2023 Apr 24;14:1172691. doi: 10.3389/fimmu.2023.1172691. eCollection 2023.
8
A Review of the Development of Multitarget Molecules against HIV-TB Coinfection Pathogens.
Molecules. 2023 Apr 10;28(8):3342. doi: 10.3390/molecules28083342.
10
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Microbiol Spectr. 2023 Jun 15;11(3):e0106623. doi: 10.1128/spectrum.01066-23. Epub 2023 Apr 10.

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