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C反应蛋白对肺炎链球菌的血液清除作用。

Blood clearance of Streptococcus pneumoniae by C-reactive protein.

作者信息

Horowitz J, Volanakis J E, Briles D E

出版信息

J Immunol. 1987 Apr 15;138(8):2598-603.

PMID:3559209
Abstract

C-reactive protein (CRP) has long been known to be an acute phase protein associated with infection and various forms of tissue damage. Recent studies have shown that human CRP can be used to passively protect mice from lethal infection with Streptococci pneumoniae. In this study we have undertaken a detailed examination of the ability of human CRP and rabbit CRP (CxRP) to mediate the blood clearance of pneumococci in mice. We have shown that the optimal activity of these acute-phase proteins requires a functioning complement system, and it can take place even in the xid mouse, which has virtually no naturally occurring anti-pneumococcal antibody in its serum. These studies provide additional evidence that CRP may play a protective role in pneumococcal infections, and it may help postpone the development of fatal levels of pneumococci in the blood, long enough for an effective anti-pneumococcal antibody response to be generated.

摘要

长期以来,人们一直认为C反应蛋白(CRP)是一种与感染及各种组织损伤形式相关的急性期蛋白。最近的研究表明,人CRP可用于被动保护小鼠免受肺炎链球菌致死性感染。在本研究中,我们详细考察了人CRP和兔CRP(CxRP)介导小鼠体内肺炎球菌血液清除的能力。我们发现,这些急性期蛋白的最佳活性需要一个功能正常的补体系统,并且即使在血清中几乎没有天然抗肺炎球菌抗体的xid小鼠中也能发生。这些研究提供了额外的证据,表明CRP可能在肺炎球菌感染中发挥保护作用,并且它可能有助于延缓血液中肺炎球菌达到致死水平的发展,时间足够长以产生有效的抗肺炎球菌抗体反应。

相似文献

1
Blood clearance of Streptococcus pneumoniae by C-reactive protein.C反应蛋白对肺炎链球菌的血液清除作用。
J Immunol. 1987 Apr 15;138(8):2598-603.
2
Blood clearance by anti-phosphocholine antibodies as a mechanism of protection in experimental pneumococcal bacteremia.抗磷酸胆碱抗体介导的血液清除作为实验性肺炎球菌菌血症的一种保护机制。
J Immunol. 1984 Dec;133(6):3308-12.
3
Human C-reactive protein is protective against fatal Streptococcus pneumoniae infection in mice.人C反应蛋白对小鼠致命性肺炎链球菌感染具有保护作用。
J Immunol. 1982 May;128(5):2374-6.
4
Human C-reactive protein is protective against fatal Streptococcus pneumoniae infection in transgenic mice.人C反应蛋白对转基因小鼠的致命性肺炎链球菌感染具有保护作用。
J Immunol. 1995 Sep 1;155(5):2557-63.
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Binding of C-reactive protein to the pneumococcal capsule or cell wall results in differential localization of C3 and stimulation of phagocytosis.C反应蛋白与肺炎球菌荚膜或细胞壁的结合导致C3的不同定位并刺激吞噬作用。
J Immunol. 1984 Sep;133(3):1424-30.
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Nitric oxide exerts distinct effects in local and systemic infections with Streptococcus pneumoniae.一氧化氮在肺炎链球菌局部感染和全身感染中发挥不同作用。
Microb Pathog. 2004 Jun;36(6):303-10. doi: 10.1016/j.micpath.2004.02.001.
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Immunization of humans with recombinant pneumococcal surface protein A (rPspA) elicits antibodies that passively protect mice from fatal infection with Streptococcus pneumoniae bearing heterologous PspA.用重组肺炎球菌表面蛋白A(rPspA)对人类进行免疫接种可引发抗体,这些抗体可被动保护小鼠免受携带异源PspA的肺炎链球菌的致命感染。
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Protection from Streptococcus pneumoniae infection by C-reactive protein and natural antibody requires complement but not Fc gamma receptors.C反应蛋白和天然抗体对肺炎链球菌感染的保护作用需要补体,但不需要Fcγ受体。
J Immunol. 2002 Jun 15;168(12):6375-81. doi: 10.4049/jimmunol.168.12.6375.
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C-reactive protein protects mice against pneumococcal infection via both phosphocholine-dependent and phosphocholine-independent mechanisms.C反应蛋白通过磷酸胆碱依赖性和非磷酸胆碱依赖性机制保护小鼠免受肺炎球菌感染。
Infect Immun. 2015 May;83(5):1845-52. doi: 10.1128/IAI.03058-14. Epub 2015 Feb 17.
10
Establishment of a Streptococcus pneumoniae nasopharyngeal colonization model in adult mice.在成年小鼠中建立肺炎链球菌鼻咽定植模型。
Microb Pathog. 1997 Sep;23(3):127-37. doi: 10.1006/mpat.1997.0142.

引用本文的文献

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2
Therapeutic Lowering of C-Reactive Protein.C 反应蛋白的治疗性降低
Front Immunol. 2021 Jan 29;11:619564. doi: 10.3389/fimmu.2020.619564. eCollection 2020.
3
Treatment of Pneumococcal Infection by Using Engineered Human C-Reactive Protein in a Mouse Model.利用工程化人 C 反应蛋白在小鼠模型中治疗肺炎球菌感染。
Front Immunol. 2020 Oct 7;11:586669. doi: 10.3389/fimmu.2020.586669. eCollection 2020.
4
Complement Activation by C-Reactive Protein Is Critical for Protection of Mice Against Pneumococcal Infection.C 反应蛋白通过补体激活对保护小鼠免受肺炎球菌感染至关重要。
Front Immunol. 2020 Aug 13;11:1812. doi: 10.3389/fimmu.2020.01812. eCollection 2020.
5
Animal models of C-reactive protein.C反应蛋白的动物模型
Mediators Inflamm. 2014;2014:683598. doi: 10.1155/2014/683598. Epub 2014 Apr 24.
6
Pentraxins: structure, function, and role in inflammation.五聚体蛋白:结构、功能及在炎症中的作用
ISRN Inflamm. 2013 Sep 14;2013:379040. doi: 10.1155/2013/379040.
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Epidemiology and long-term clinical and biologic risk factors for pneumonia in community-dwelling older Americans: analysis of three cohorts.美国社区居住的老年人肺炎的流行病学和长期临床及生物学危险因素:三个队列的分析。
Chest. 2013 Sep;144(3):1008-1017. doi: 10.1378/chest.12-2818.
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The phosphocholine-binding pocket on C-reactive protein is necessary for initial protection of mice against pneumococcal infection.C 反应蛋白上的磷酸胆碱结合口袋对于最初保护小鼠免受肺炎球菌感染是必要的。
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Respirology. 2010 Jan;15(1):160-4. doi: 10.1111/j.1440-1843.2009.01661.x. Epub 2009 Nov 23.