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M(+)组A群链球菌在全血中被C5a激活的多形核白细胞吞噬并杀死。

M(+) group a streptococci are phagocytized and killed in whole blood by C5a-activated polymorphonuclear leukocytes.

作者信息

DeMaster Eric, Schnitzler Norbert, Cheng Qi, Cleary Patrick

机构信息

Department of Microbiology, University of Minnesota, Minneapolis, Minnesota 55455, USA.

出版信息

Infect Immun. 2002 Jan;70(1):350-9. doi: 10.1128/IAI.70.1.350-359.2002.

Abstract

Historically, resistance to phagocytosis has been determined by incubating group A streptococci in human blood and comparing the numbers of CFU before and after incubation. Utilizing a flow cytometry-based technique, we have investigated the phagocytosis of M(+) group A streptococci by polymorphonuclear leukocytes (PMNs) in heparinized human peripheral whole blood. Intracellular labeling of streptococci with a nontoxic fluorescent dye allowed us to quantify the association and phagocytosis of M(+) streptococci by PMNs in whole blood in the presence or absence of C5a, a physiologically important chemotactic activator of PMNs. We found that wild-type strains of group A streptococci that are resistant to phagocytosis (determined by the classical Lancefield method) readily associate with C5a-activated whole-blood PMNs. In the absence of opsonizing M-type-specific antibodies, the M(+) streptococci associated with PMNs are phagocytized and killed. In addition, blockade of the beta(2) integrin, CD11b/CD18, with anti-human CD11b monoclonal antibody inhibited association between M(+) streptococci and C5a-activated PMNs. These findings establish a new relationship between M(+) streptococci and PMNs, in which C5a-activated PMNs have the capacity to kill M(+) streptococci in whole blood through a receptor-mediated phagocytic mechanism.

摘要

从历史上看,对吞噬作用的抗性是通过将A组链球菌在人血液中孵育,并比较孵育前后的菌落形成单位(CFU)数量来确定的。利用基于流式细胞术的技术,我们研究了肝素化人外周全血中多形核白细胞(PMN)对M(+)A组链球菌的吞噬作用。用无毒荧光染料对链球菌进行细胞内标记,使我们能够在有或没有C5a(PMN一种重要的生理趋化激活剂)存在的情况下,定量全血中PMN对M(+)链球菌的结合和吞噬作用。我们发现,对吞噬作用有抗性的A组链球菌野生型菌株(通过经典的兰斯菲尔德方法确定)很容易与C5a激活的全血PMN结合。在没有调理素M型特异性抗体的情况下,与PMN结合的M(+)链球菌会被吞噬并杀死。此外,用抗人CD11b单克隆抗体阻断β2整合素CD11b/CD18可抑制M(+)链球菌与C5a激活的PMN之间的结合。这些发现建立了M(+)链球菌与PMN之间的新关系,其中C5a激活的PMN有能力通过受体介导的吞噬机制在全血中杀死M(+)链球菌。

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