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血清杀菌活性及多形核白细胞化学发光的诱导:防御脑膜炎奈瑟菌时补体激活途径的要求

Serum bactericidal activity and induction of chemiluminescence of polymorphonuclear leukocytes: complement activation pathway requirements in defense against Neisseria meningitidis.

作者信息

Fredlund H, Sjöholm A G, Selander B, Holmström E, Olcén P, Danielsson D

机构信息

Department of Clinical Microbiology and Immunology, Orebro Medical Center Hospital, Sweden.

出版信息

Int Arch Allergy Immunol. 1993;100(2):135-43. doi: 10.1159/000236400.

Abstract

Serum bactericidal activity and chemiluminescence (CL) responses of polymorphonuclear leukocytes (PMNL) to pathogenic Neisseria meningitidis serogroups B and W-135 and to nonpathogenic serogroup 29E were examined with pooled normal human serum depleted of the complement proteins C1q, factor D, properdin and C5. Purified C1q, factor D, properdin and C5 were added alone or in combination. For investigation of serogroup W-135 meningococci, a C1q, factor D and properdin-depleted postvaccination serum with high concentrations of anticapsular antibodies was also used. Serogroup B and W-135 cultured to log phase were resistant to the bactericidal activity of pooled normal human serum but were efficiently killed through the classical pathway alone when the bacteria were cultured to stationary phase. Nonpathogenic serogroup 29E meningococci in log or stationary growth phases were efficiently killed in serum, predominantly through the classical pathway. Serogroup W-135 meningococci grown to log phase were resistant to classical pathway-mediated bactericidal activity in postvaccination serum but were killed on addition of alternative pathway proteins. Stationary phase serogroup W-135 meningococci were killed through both pathways in the postvaccination serum. In the pooled normal human serum CL responses of PMNL were consistently more pronounced with fully reconstituted C1q, factor D, properdin, C5-depleted serum than with serum reconstituted with C1q, factor D and properdin suggesting contribution of actions related to terminal components. In the absence of C1q, serogroup W-135 meningococci in postvaccination serum induced a significant but delayed alternative pathway-mediated CL response. CL responses induced by serum-opsonized meningococci, in contrast to serum bactericidal activity, were not influenced by culture conditions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用去除补体蛋白C1q、因子D、备解素和C5的混合正常人血清,检测多形核白细胞(PMNL)对致病性B群和W-135群脑膜炎奈瑟菌以及非致病性29E群脑膜炎奈瑟菌的血清杀菌活性和化学发光(CL)反应。单独或组合添加纯化的C1q、因子D、备解素和C5。为研究W-135群脑膜炎球菌,还使用了含有高浓度抗荚膜抗体的去除C1q、因子D和备解素的疫苗接种后血清。培养至对数期的B群和W-135群对混合正常人血清的杀菌活性具有抗性,但当细菌培养至稳定期时,仅通过经典途径就可被有效杀灭。处于对数期或稳定期生长的非致病性29E群脑膜炎球菌在血清中主要通过经典途径被有效杀灭。生长至对数期的W-135群脑膜炎球菌对疫苗接种后血清中经典途径介导的杀菌活性具有抗性,但添加替代途径蛋白后可被杀死。稳定期的W-135群脑膜炎球菌在疫苗接种后血清中可通过两条途径被杀死。在混合正常人血清中,与用C1q、因子D和备解素重构的血清相比,完全重构C1q、因子D、备解素、C5缺失血清时PMNL的CL反应始终更明显,提示与终末成分相关的作用有贡献。在缺乏C1q的情况下,疫苗接种后血清中的W-135群脑膜炎球菌诱导了显著但延迟的替代途径介导的CL反应。与血清杀菌活性相反,血清调理的脑膜炎球菌诱导的CL反应不受培养条件影响。(摘要截短至250字)

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