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IL-17 and Th17 cells in tuberculosis.结核中的白细胞介素-17 和 Th17 细胞。
Cytokine Growth Factor Rev. 2010 Dec;21(6):455-62. doi: 10.1016/j.cytogfr.2010.10.004. Epub 2010 Nov 12.
2
Mycobacterium bovis BCG-specific Th17 cells confer partial protection against Mycobacterium tuberculosis infection in the absence of gamma interferon.牛分枝杆菌卡介苗特异性 Th17 细胞在缺乏γ干扰素的情况下对结核分枝杆菌感染提供部分保护。
Infect Immun. 2010 Oct;78(10):4187-94. doi: 10.1128/IAI.01392-09. Epub 2010 Aug 2.
3
Expanded polyfunctional T cell response to mycobacterial antigens in TB disease and contraction post-treatment.在结核病发病时和治疗后,针对分枝杆菌抗原的扩展多功能 T 细胞反应。
PLoS One. 2010 Jun 21;5(6):e11237. doi: 10.1371/journal.pone.0011237.
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Human T cell epitopes of Mycobacterium tuberculosis are evolutionarily hyperconserved.结核分枝杆菌的人类 T 细胞表位具有进化上的高度保守性。
Nat Genet. 2010 Jun;42(6):498-503. doi: 10.1038/ng.590. Epub 2010 May 23.
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Tuberculosis: what we don't know can, and does, hurt us.结核病:我们不知道的,确实会伤害我们。
Science. 2010 May 14;328(5980):852-6. doi: 10.1126/science.1184784.
6
Essential role of IL-17A in the formation of a mycobacterial infection-induced granuloma in the lung.IL-17A 在肺中分枝杆菌感染诱导的肉芽肿形成中的重要作用。
J Immunol. 2010 Apr 15;184(8):4414-22. doi: 10.4049/jimmunol.0903332. Epub 2010 Mar 8.
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TB: screening for responses to a vile visitor.TB:对恶劣访客的反应进行筛查。
Cell. 2010 Mar 5;140(5):615-8. doi: 10.1016/j.cell.2010.02.030.
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Chemotherapy rescues tumor-driven aberrant CD4+ T-cell differentiation and restores an activated polyfunctional helper phenotype.化疗挽救肿瘤驱动的异常 CD4+ T 细胞分化,并恢复活化的多功能辅助表型。
Blood. 2010 Mar 25;115(12):2397-406. doi: 10.1182/blood-2009-11-253336. Epub 2010 Jan 29.
9
Cyclophosphamide induces dynamic alterations in the host microenvironments resulting in a Flt3 ligand-dependent expansion of dendritic cells.环磷酰胺可诱导宿主微环境发生动态变化,导致树突状细胞在Flt3配体依赖的情况下扩增。
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10
Mapping the global use of different BCG vaccine strains.绘制全球不同卡介苗菌株使用情况的图谱。
Tuberculosis (Edinb). 2009 Jul;89(4):248-51. doi: 10.1016/j.tube.2009.03.002. Epub 2009 Jun 18.

体外培养基会影响牛分枝杆菌卡介苗的疫苗效力。

In vitro culture medium influences the vaccine efficacy of Mycobacterium bovis BCG.

机构信息

Department of Microbiology and Immunology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Vaccine. 2012 Feb 1;30(6):1038-49. doi: 10.1016/j.vaccine.2011.12.044. Epub 2011 Dec 18.

DOI:10.1016/j.vaccine.2011.12.044
PMID:22189700
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3269512/
Abstract

The varied rates of protection induced by Mycobacterium bovis BCG vaccine against tuberculosis has been attributed to many factors such as genetic variability among BCG strains, rapid clearance of BCG in some populations, and different levels of previous exposure of vaccinated populations to environmental mycobacteria. However, the methods and conditions employed to prepare this vaccine for human usage by various manufacturers have not been investigated as potential factors contributing to the variation in vaccine efficacy. A review of the literature indicates discrepancies between the approach for growing BCG vaccine in the laboratory to assess immune responses and protective ability in animal models, and that employed for production of the vaccine for administration to humans. One of the major differences is in the growth medium used for routine propagation in the laboratory and the one used for bulk vaccine production by manufacturers. Here we compared the immunogenicity of the BCG vaccine grown in Middlebrook 7H9 medium, the most commonly used medium in laboratory studies, against that grown in Sauton medium, which is used for growing BCG by most manufacturers. Our results showed clear differences in the behavior of BCG grown in these different culture media. Compared to BCG grown in Middlebrook 7H9 medium, BCG grown in Sauton media was more persistent inside macrophages, more effective at inhibiting apoptosis of infected cells, induced stronger inflammatory responses and stimulated less effective immunity against aerosol challenge with a virulent Mtb strain. These findings suggested that the growth medium used for producing BCG vaccine is an important factor that deserves increased scrutiny in ongoing efforts to produce more consistently effective vaccines against Mtb.

摘要

牛型结核分枝杆菌卡介苗(BCG)疫苗对结核病的保护率存在差异,其原因有很多,如 BCG 菌株的遗传变异性、某些人群中 BCG 的快速清除、以及接种人群对环境分枝杆菌的既往暴露程度不同等。然而,不同制造商用于制备人类 BCG 疫苗的方法和条件尚未被视为导致疫苗效力差异的潜在因素。文献综述表明,实验室中用于评估免疫反应和动物模型保护能力的 BCG 疫苗培养方法与用于向人类接种疫苗的生产方法之间存在差异。其中一个主要区别是在实验室中常规繁殖中使用的生长培养基与制造商用于批量生产疫苗的培养基之间的差异。在这里,我们比较了在最常用于实验室研究的 Middlebrook 7H9 培养基中生长的 BCG 疫苗与在大多数制造商用于生长 BCG 的 Sauton 培养基中生长的 BCG 的免疫原性。我们的结果表明,在这些不同的培养基中生长的 BCG 行为存在明显差异。与在 Middlebrook 7H9 培养基中生长的 BCG 相比,在 Sauton 培养基中生长的 BCG 在巨噬细胞内更持久,更有效地抑制感染细胞的凋亡,诱导更强的炎症反应,并刺激对有活力的 Mtb 菌株气溶胶挑战的免疫应答效果较差。这些发现表明,用于生产 BCG 疫苗的生长培养基是一个重要因素,值得在生产更一致有效的 Mtb 疫苗的持续努力中进一步研究。