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2
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本文引用的文献

1
Macrophage arginase-1 controls bacterial growth and pathology in hypoxic tuberculosis granulomas.巨噬细胞精氨酸酶-1控制缺氧结核肉芽肿中的细菌生长和病理状况。
Proc Natl Acad Sci U S A. 2014 Sep 23;111(38):E4024-32. doi: 10.1073/pnas.1408839111. Epub 2014 Sep 8.
2
Graded levels of IRF4 regulate CD8+ T cell differentiation and expansion, but not attrition, in response to acute virus infection.IRF4 呈梯度水平调节 CD8+T 细胞分化和扩增,但不影响其在急性病毒感染时的耗竭。
J Immunol. 2014 Jun 15;192(12):5881-93. doi: 10.4049/jimmunol.1303187. Epub 2014 May 16.
3
Characterization of a novel necrotic granuloma model of latent tuberculosis infection and reactivation in mice.小鼠潜伏性结核感染和再激活的新型坏死性肉芽肿模型的特征描述。
Am J Pathol. 2014 Jul;184(7):2045-55. doi: 10.1016/j.ajpath.2014.03.008. Epub 2014 May 9.
4
Early Changes by (18)Fluorodeoxyglucose positron emission tomography coregistered with computed tomography predict outcome after Mycobacterium tuberculosis infection in cynomolgus macaques.(18)F 氟代脱氧葡萄糖正电子发射断层扫描与计算机断层扫描融合早期改变预测猕猴结核分枝杆菌感染的结局。
Infect Immun. 2014 Jun;82(6):2400-4. doi: 10.1128/IAI.01599-13. Epub 2014 Mar 24.
5
Clonotype-specific avidity influences the dynamics and hierarchy of virus-specific regulatory and effector CD4(+) T-cell responses.克隆型特异性亲和力影响病毒特异性调节性和效应性CD4(+) T细胞反应的动力学和层次结构。
Eur J Immunol. 2014 Apr;44(4):1058-68. doi: 10.1002/eji.201343766. Epub 2014 Feb 8.
6
CD4+ T cells contain early extrapulmonary tuberculosis (TB) dissemination and rapid TB progression and sustain multieffector functions of CD8+ T and CD3- lymphocytes: mechanisms of CD4+ T cell immunity.CD4+ T 细胞含有早期肺外结核(TB)传播和快速 TB 进展,并维持 CD8+ T 和 CD3- 淋巴细胞的多效性功能:CD4+ T 细胞免疫的机制。
J Immunol. 2014 Mar 1;192(5):2120-32. doi: 10.4049/jimmunol.1301373. Epub 2014 Jan 31.
7
A review of preclinical animal models utilised for TB vaccine evaluation in the context of recent human efficacy data.对近期人类疗效数据背景下用于结核病疫苗评估的临床前动物模型的综述。
Tuberculosis (Edinb). 2014 Mar;94(2):105-10. doi: 10.1016/j.tube.2013.11.003. Epub 2013 Dec 1.
8
Sterilization of granulomas is common in active and latent tuberculosis despite within-host variability in bacterial killing.尽管宿主内细菌杀伤存在变异性,但在活动性和潜伏性结核中,肉芽肿的灭菌很常见。
Nat Med. 2014 Jan;20(1):75-9. doi: 10.1038/nm.3412. Epub 2013 Dec 15.
9
Is tuberculosis a lymphatic disease with a pulmonary portal?肺结核是一种具有肺门淋巴结的淋巴系统疾病吗?
Lancet Infect Dis. 2014 Mar;14(3):250-5. doi: 10.1016/S1473-3099(13)70253-6. Epub 2013 Nov 22.
10
Essential yet limited role for CCR2⁺ inflammatory monocytes during Mycobacterium tuberculosis-specific T cell priming.CCR2⁺ 炎性单核细胞在结核分枝杆菌特异性T细胞启动过程中起重要但有限的作用。
Elife. 2013 Nov 12;2:e01086. doi: 10.7554/eLife.01086.

结核病非人灵长类动物模型的免疫学研究

Immunology studies in non-human primate models of tuberculosis.

作者信息

Flynn JoAnne L, Gideon Hannah P, Mattila Joshua T, Lin Philana Ling

机构信息

Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

出版信息

Immunol Rev. 2015 Mar;264(1):60-73. doi: 10.1111/imr.12258.

DOI:10.1111/imr.12258
PMID:25703552
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4339213/
Abstract

Non-human primates, primarily macaques, have been used to study tuberculosis for decades. However, in the last 15 years, this model has been refined substantially to allow careful investigations of the immune response and host-pathogen interactions in Mycobacterium tuberculosis infection. Low-dose challenge with fully virulent strains in cynomolgus macaques result in the full clinical spectrum seen in humans, including latent and active infection. Reagents from humans are usually cross-reactive with macaques, further facilitating the use of this model system to study tuberculosis. Finally, macaques develop the spectrum of granuloma types seen in humans, providing a unique opportunity to investigate bacterial and host factors at the local (lung and lymph node) level. Here, we review the past decade of immunology and pathology studies in macaque models of tuberculosis.

摘要

几十年来,非人类灵长类动物,主要是猕猴,一直被用于研究结核病。然而,在过去15年中,该模型得到了大幅改进,以便能够仔细研究结核分枝杆菌感染中的免疫反应和宿主-病原体相互作用。用完全有毒力的菌株对食蟹猴进行低剂量攻击会导致出现人类中所见的完整临床谱,包括潜伏感染和活动性感染。来自人类的试剂通常与猕猴具有交叉反应性,这进一步促进了利用该模型系统来研究结核病。最后,猕猴会形成人类中所见的各种肉芽肿类型,这为在局部(肺和淋巴结)水平研究细菌和宿主因素提供了独特的机会。在此,我们回顾过去十年在猕猴结核病模型中的免疫学和病理学研究。