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宿主对分枝杆菌抗原的免疫反应及其对开发控制结核病疫苗的意义。

Host immune responses to mycobacterial antigens and their implications for the development of a vaccine to control tuberculosis.

作者信息

Yuk Jae-Min, Jo Eun-Kyeong

机构信息

Department of Microbiology and Infection Signaling Network Research Center, Chungnam National University School of Medicine, Daejeon, Korea.

出版信息

Clin Exp Vaccine Res. 2014 Jul;3(2):155-67. doi: 10.7774/cevr.2014.3.2.155. Epub 2014 Jun 20.

DOI:10.7774/cevr.2014.3.2.155
PMID:25003089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4083068/
Abstract

Tuberculosis (TB) remains a worldwide health problem, causing around 2 million deaths per year. Despite the bacillus Calmette Guérin vaccine being available for more than 80 years, it has limited effectiveness in preventing TB, with inconsistent results in trials. This highlights the urgent need to develop an improved TB vaccine, based on a better understanding of host-pathogen interactions and immune responses during mycobacterial infection. Recent studies have revealed a potential role for autophagy, an intracellular homeostatic process, in vaccine development against TB, through enhanced immune activation. This review attempts to understand the host innate immune responses induced by a variety of protein antigens from Mycobacterium tuberculosis, and to identify future vaccine candidates against TB. We focus on recent advances in vaccine development strategies, through identification of new TB antigens using a variety of innovative tools. A new understanding of the host-pathogen relationship, and the usefulness of mycobacterial antigens as novel vaccine candidates, will contribute to the design of the next generation of vaccines, and to improving the host protective immune responses while limiting immunopathology during M. tuberculosis infection.

摘要

结核病仍然是一个全球性的健康问题,每年导致约200万人死亡。尽管卡介苗已经问世80多年,但它在预防结核病方面效果有限,试验结果并不一致。这凸显了基于对分枝杆菌感染期间宿主-病原体相互作用和免疫反应的更好理解来开发改进型结核病疫苗的迫切需求。最近的研究揭示了自噬(一种细胞内稳态过程)通过增强免疫激活在结核病疫苗开发中的潜在作用。本综述试图了解结核分枝杆菌的多种蛋白质抗原诱导的宿主固有免疫反应,并确定未来的结核病候选疫苗。我们通过使用各种创新工具鉴定新的结核抗原,关注疫苗开发策略的最新进展。对宿主-病原体关系的新认识以及分枝杆菌抗原作为新型候选疫苗的实用性,将有助于设计下一代疫苗,并在结核分枝杆菌感染期间增强宿主保护性免疫反应的同时限制免疫病理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3034/4083068/64cbeab94e37/cevr-3-155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3034/4083068/64cbeab94e37/cevr-3-155-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3034/4083068/64cbeab94e37/cevr-3-155-g001.jpg

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本文引用的文献

1
Pattern recognition receptors and cytokines in Mycobacterium tuberculosis infection--the double-edged sword?结核分枝杆菌感染中的模式识别受体和细胞因子——双刃剑?
Biomed Res Int. 2013;2013:179174. doi: 10.1155/2013/179174. Epub 2013 Nov 12.
2
Vaccine activation of the nutrient sensor GCN2 in dendritic cells enhances antigen presentation.疫苗激活树突状细胞中的营养传感器 GCN2 可增强抗原呈递。
Science. 2014 Jan 17;343(6168):313-317. doi: 10.1126/science.1246829. Epub 2013 Dec 5.
3
Immunogenic potential of latency associated antigens against Mycobacterium tuberculosis.
结核分枝杆菌特异性ESAT6样蛋白的化学和生物学特性及其在预防结核病和哮喘中的潜力
Med Princ Pract. 2023 Sep 13;32(4-5):217-24. doi: 10.1159/000534002.
4
A Dendritic Cell-Activating Rv1876 Protein Elicits Mycobacterium Bovis BCG-Prime Effect via Th1-Immune Response.一种树突状细胞激活蛋白 Rv1876 可通过 Th1 免疫应答引发牛分枝杆菌卡介苗的增效作用。
Biomolecules. 2021 Sep 3;11(9):1306. doi: 10.3390/biom11091306.
5
Targeting Autophagy as a Strategy for Developing New Vaccines and Host-Directed Therapeutics Against Mycobacteria.靶向自噬作为开发抗分枝杆菌新疫苗和宿主导向疗法的策略。
Front Microbiol. 2021 Jan 14;11:614313. doi: 10.3389/fmicb.2020.614313. eCollection 2020.
6
Fusion of Dendritic Cells Activating Rv2299c Protein Enhances the Protective Immunity of Ag85B-ESAT6 Vaccine Candidate against Tuberculosis.激活Rv2299c蛋白的树突状细胞融合增强了候选疫苗Ag85B-ESAT6对结核病的保护性免疫。
Pathogens. 2020 Oct 22;9(11):865. doi: 10.3390/pathogens9110865.
7
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Afr J Infect Dis. 2019 Jul 3;13(2):13-20. doi: 10.21010/ajid.v13i2.2. eCollection 2019.
8
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Proc Natl Acad Sci U S A. 2019 Mar 26;116(13):6371-6378. doi: 10.1073/pnas.1811380116. Epub 2019 Mar 8.
9
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J Biol Chem. 2018 Jun 29;293(26):10287-10302. doi: 10.1074/jbc.RA118.001696. Epub 2018 May 8.
10
Next generation sequencing reveals changes of the γδ T cell receptor repertoires in patients with pulmonary tuberculosis.下一代测序揭示了肺结核患者 γδ T 细胞受体库的变化。
Sci Rep. 2018 Mar 2;8(1):3956. doi: 10.1038/s41598-018-22061-x.
潜伏相关抗原对结核分枝杆菌的免疫原性。
Vaccine. 2014 Feb 3;32(6):712-6. doi: 10.1016/j.vaccine.2013.11.065. Epub 2013 Dec 2.
4
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Front Immunol. 2013 Oct 11;4:335. doi: 10.3389/fimmu.2013.00335.
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Vaccine. 2013 Dec 2;31(49):5848-55. doi: 10.1016/j.vaccine.2013.09.069. Epub 2013 Oct 10.
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Vaccine. 2013 Oct 1;31(42):4867-73. doi: 10.1016/j.vaccine.2013.07.051. Epub 2013 Aug 17.
8
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J Control Release. 2013 Nov 28;172(1):190-200. doi: 10.1016/j.jconrel.2013.07.030. Epub 2013 Aug 9.
9
Multiple antigen-presenting system (MAPS) to induce comprehensive B- and T-cell immunity.多重抗原呈递系统(MAPS)诱导全面的 B 细胞和 T 细胞免疫。
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10
Mycobacterium tuberculosis RpfB drives Th1-type T cell immunity via a TLR4-dependent activation of dendritic cells.结核分枝杆菌 RpfB 通过 TLR4 依赖性树突状细胞激活驱动 Th1 型 T 细胞免疫。
J Leukoc Biol. 2013 Oct;94(4):733-49. doi: 10.1189/jlb.0912435. Epub 2013 Jul 3.