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全血模型。

Whole-blood model.

作者信息

Ison C A

机构信息

Department of Infectious Diseases ⇐p; Microbiology, Imperial College School of Medicine, London, UK.

出版信息

Methods Mol Med. 2001;66:317-29. doi: 10.1385/1-59259-148-5:317.

DOI:10.1385/1-59259-148-5:317
PMID:21336764
Abstract

Neisseria meningitidis is an obligate human pathogen. When it interacts with the host, it can establish a commensal relationship or can, on a minority of occasions, invade and cause systemic disease. Protection against systemic disease, particularly for serogroup A and C infections, has been equated with the presence of bactericidal antibody directed against the capsular polysaccharide (CPS) (1). In serogroup B infections, the CPS resembles host-cell moieties, is non-immunogenic, and does not induce protection (2). Hence other components of the bacterial-cell envelope, such as outer-membrane proteins (OMPs), and cellular mechanisms of host defense, such as phagocytosis, have been implicated in immunity to serogroup B infections (3,4).

摘要

脑膜炎奈瑟菌是一种专性人类病原体。当它与宿主相互作用时,它可以建立共生关系,或者在少数情况下,侵入并引起全身性疾病。预防全身性疾病,特别是针对A群和C群感染,已等同于存在针对荚膜多糖(CPS)的杀菌抗体(1)。在B群感染中,CPS类似于宿主细胞成分,无免疫原性,不诱导保护作用(2)。因此,细菌细胞膜的其他成分,如外膜蛋白(OMPs),以及宿主防御的细胞机制,如吞噬作用,已被认为与B群感染的免疫有关(3,4)。

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1
Whole-blood model.全血模型。
Methods Mol Med. 2001;66:317-29. doi: 10.1385/1-59259-148-5:317.
2
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引用本文的文献

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Analysis of the regulated transcriptome of Neisseria meningitidis in human blood using a tiling array.利用基因芯片分析脑膜炎奈瑟菌在人血中的调控转录组。
J Bacteriol. 2012 Nov;194(22):6217-32. doi: 10.1128/JB.01055-12. Epub 2012 Sep 14.
2
A cyanobacterial lipopolysaccharide antagonist inhibits cytokine production induced by Neisseria meningitidis in a human whole-blood model of septicemia.一种蓝藻脂多糖拮抗剂在人类败血症全血模型中可抑制脑膜炎奈瑟菌诱导的细胞因子产生。
Infect Immun. 2008 Jul;76(7):3156-63. doi: 10.1128/IAI.00110-08. Epub 2008 Apr 28.