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结核病疫苗:超越卡介苗。

Tuberculosis vaccines: beyond bacille Calmette-Guerin.

机构信息

The Jenner Institute, University of Oxford, Old Road Campus Research Building, Oxford OX3 7DQ, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2011 Oct 12;366(1579):2782-9. doi: 10.1098/rstb.2011.0097.


DOI:10.1098/rstb.2011.0097
PMID:21893541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3146779/
Abstract

Tuberculosis (TB) disease caused by Mycobacterium tuberculosis (M. tb) remains one of the leading infectious causes of death and disease throughout the world. The only licensed vaccine, Mycobacterium bovis bacille Calmette-Guérin (BCG) confers highly variable protection against pulmonary disease. An effective vaccination regimen would be the most efficient way to control the epidemic. However, BCG does confer consistent and reliable protection against disseminated disease in childhood, and most TB vaccine strategies being developed incorporate BCG to retain this protection. Cellular immunity is necessary for protection against TB and all the new vaccines in development are focused on inducing a strong and durable cellular immune response. There are two main strategies being pursued in TB vaccine development. The first is to replace BCG with an improved whole organism mycobacterial priming vaccine, which is either a recombinant BCG or an attenuated strain of M. tb. The second is to develop a subunit boosting vaccine, which is designed to be administered after BCG vaccination, and to enhance the protective efficacy of BCG. This article reviews the leading candidate vaccines in development and considers the current challenges in the field with regard to efficacy testing.

摘要

结核病(TB)是由结核分枝杆菌(M. tb)引起的疾病,仍然是全球主要的传染病死因和疾病之一。唯一获得许可的疫苗,牛分枝杆菌卡介苗(BCG)对肺部疾病的保护作用差异很大。有效的疫苗接种方案将是控制该流行病的最有效方法。然而,BCG 确实在儿童期对传播性疾病提供一致且可靠的保护,并且正在开发的大多数结核病疫苗策略都包含 BCG 以保留这种保护。细胞免疫是预防结核病所必需的,所有正在开发的新型疫苗都专注于诱导强烈和持久的细胞免疫反应。在结核病疫苗开发中有两种主要策略。第一种是用改良的全菌体分枝杆菌初免疫苗替代 BCG,该疫苗是重组 BCG 或减毒的结核分枝杆菌菌株。第二种是开发亚单位增强疫苗,旨在在 BCG 接种后使用,以增强 BCG 的保护效果。本文综述了正在开发的主要候选疫苗,并考虑了该领域在功效测试方面的当前挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df1/3146779/09ac4487d6e7/rstb20110097-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df1/3146779/09ac4487d6e7/rstb20110097-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9df1/3146779/09ac4487d6e7/rstb20110097-g1.jpg

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Tuberculosis vaccines: beyond bacille Calmette-Guerin.

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[4]
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[6]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Evaluation of the safety and immunogenicity of two antigen concentrations of the Mtb72F/AS02(A) candidate tuberculosis vaccine in purified protein derivative-negative adults.

Clin Vaccine Immunol. 2010-11

[2]
Specific T cell frequency and cytokine expression profile do not correlate with protection against tuberculosis after bacillus Calmette-Guérin vaccination of newborns.

Am J Respir Crit Care Med. 2010-6-17

[3]
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Vaccine. 2010-3-11

[4]
The novel tuberculosis vaccine, AERAS-402, induces robust and polyfunctional CD4+ and CD8+ T cells in adults.

Am J Respir Crit Care Med. 2010-2-18

[5]
Prevention of tuberculosis in Bacille Calmette-Guérin-primed, HIV-infected adults boosted with an inactivated whole-cell mycobacterial vaccine.

AIDS. 2010-3-13

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Vaccine. 2010-1-20

[7]
Modified vaccinia Ankara-expressing Ag85A, a novel tuberculosis vaccine, is safe in adolescents and children, and induces polyfunctional CD4+ T cells.

Eur J Immunol. 2010-1

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Hum Vaccin. 2009-7

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PLoS One. 2009-6-16

[10]
Efficacy and safety of live attenuated persistent and rapidly cleared Mycobacterium tuberculosis vaccine candidates in non-human primates.

Vaccine. 2009-7-23

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