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本文引用的文献

1
Mycobacterium bovis BCG-mediated protection against W-Beijing strains of Mycobacterium tuberculosis is diminished concomitant with the emergence of regulatory T cells.牛分枝杆菌卡介苗介导的针对北京基因型结核分枝杆菌菌株的保护作用会随着调节性T细胞的出现而减弱。
Clin Vaccine Immunol. 2011 Sep;18(9):1527-35. doi: 10.1128/CVI.05127-11. Epub 2011 Jul 27.
2
A multistage tuberculosis vaccine that confers efficient protection before and after exposure.一种多阶段结核疫苗,可在暴露前后提供高效保护。
Nat Med. 2011 Feb;17(2):189-94. doi: 10.1038/nm.2285. Epub 2011 Jan 23.
3
A defined tuberculosis vaccine candidate boosts BCG and protects against multidrug-resistant Mycobacterium tuberculosis.一种有明确特征的结核候选疫苗可增强卡介苗的效果,并预防耐多药结核分枝杆菌。
Sci Transl Med. 2010 Oct 13;2(53):53ra74. doi: 10.1126/scitranslmed.3001094.
4
The Achilles heel of BCG.卡介苗的阿喀琉斯之踵。
Tuberculosis (Edinb). 2010 Nov;90(6):329-32. doi: 10.1016/j.tube.2010.06.002. Epub 2010 Jul 24.
5
Pulmonary immunization using antigen 85-B polymeric microparticles to boost tuberculosis immunity.使用抗原 85-B 聚合体微球进行肺部免疫接种以增强结核病免疫力。
AAPS J. 2010 Sep;12(3):338-47. doi: 10.1208/s12248-010-9193-1. Epub 2010 Apr 27.
6
Neonatal BCG immunization followed by DNAhsp65 boosters: highly immunogenic but not protective against tuberculosis - a paradoxical effect of the vector?新生儿卡介苗免疫接种后再用 DNAhsp65 加强免疫:具有高度免疫原性,但不能预防结核病——载体的矛盾作用?
Scand J Immunol. 2010 Feb;71(2):63-9. doi: 10.1111/j.1365-3083.2009.02352.x.
7
Highly persistent and effective prime/boost regimens against tuberculosis that use a multivalent modified vaccine virus Ankara-based tuberculosis vaccine with interleukin-15 as a molecular adjuvant.使用基于多价修饰安卡拉疫苗病毒并以白细胞介素-15作为分子佐剂的高效持久抗结核初免/加强免疫方案。
Clin Vaccine Immunol. 2010 May;17(5):793-801. doi: 10.1128/CVI.00006-10. Epub 2010 Mar 31.
8
Non-clinical efficacy and safety of HyVac4:IC31 vaccine administered in a BCG prime-boost regimen.卡介苗初免-加强免疫程序中接种 HyVac4:IC31 疫苗的非临床疗效和安全性。
Vaccine. 2010 Jan 22;28(4):1084-93. doi: 10.1016/j.vaccine.2009.10.114. Epub 2009 Nov 5.
9
Boosting with a DNA vaccine expressing ESAT-6 (DNAE6) obliterates the protection imparted by recombinant BCG (rBCGE6) against aerosol Mycobacterium tuberculosis infection in guinea pigs.用表达 ESAT-6 的 DNA 疫苗(DNAE6)进行增强会消除重组卡介苗(rBCGE6)对豚鼠气溶胶分枝杆菌感染的保护作用。
Vaccine. 2009 Dec 10;28(1):63-70. doi: 10.1016/j.vaccine.2009.09.121. Epub 2009 Oct 15.
10
Mycobacterium tuberculosis culture filtrate proteins plus CpG Oligodeoxynucleotides confer protection to Mycobacterium bovis BCG-primed mice by inhibiting interleukin-4 secretion.结核分枝杆菌培养滤液蛋白加CpG寡脱氧核苷酸通过抑制白细胞介素-4分泌对卡介苗致敏小鼠起到保护作用。
Infect Immun. 2009 Dec;77(12):5311-21. doi: 10.1128/IAI.00580-09. Epub 2009 Sep 14.

结核病疫苗策略实施的临床前证据。

Preclinical evidence for implementing a prime-boost vaccine strategy for tuberculosis.

机构信息

Aeras, Rockville, MD 20850, USA.

出版信息

Vaccine. 2012 Apr 16;30(18):2811-23. doi: 10.1016/j.vaccine.2012.02.036. Epub 2012 Mar 3.

DOI:10.1016/j.vaccine.2012.02.036
PMID:22387630
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3335191/
Abstract

In this review, published peer-reviewed preclinical studies using prime-boost tuberculosis (TB) vaccine regimens in animal challenge models for tuberculosis have been evaluated. These studies have been divided into groups that describe prime-boost vaccine combinations that performed better than, equivalent to, or worse than the currently used BCG vaccine. Review of the data has revealed interesting findings, including that more than half of the published studies using BCG as a prime combined with a novel boost vaccine give better efficacy than BCG alone and that the greatest reduction in Mycobacterium tuberculosis (M.tb.) colonization of animal tissues is provided by viral vectored vaccines delivered intranasally. Careful evaluation of these data should assist in defining the value of prime-boost regimens for advancement into human TB vaccine trials and stimulate the development of criteria for choosing which vaccine candidates should be studied further.

摘要

在这篇综述中,评估了已发表的使用在动物挑战模型中针对结核病的加强型结核(TB)疫苗方案的同行评审临床前研究。这些研究分为描述加强型疫苗组合的组,这些疫苗组合在效果上优于、等同于或劣于目前使用的卡介苗(BCG)疫苗。对数据的审查揭示了有趣的发现,包括超过一半的使用卡介苗作为初始疫苗并结合新型加强疫苗的已发表研究比单独使用卡介苗的效果更好,并且通过鼻腔内给予病毒载体疫苗可以最大程度地减少动物组织中结核分枝杆菌(M.tb.)的定植。对这些数据的仔细评估应该有助于确定加强型疫苗方案在推进人类结核病疫苗试验中的价值,并激发制定选择应进一步研究哪些疫苗候选物的标准。