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淋病奈瑟菌的血清杀菌作用及经典和替代补体途径的激活

Serum bactericidal action and activation of the classic and alternate complement pathways by Neisseria gonorrhoeae.

作者信息

Ingwer I, Petersen B H, Brooks G

出版信息

J Lab Clin Med. 1978 Aug;92(2):211-20.

PMID:98602
Abstract

In order to more fully understand the host defense mechanisms against gonococcal infections, we decided to define the role of the classic and alternate complement pathways in gonococcal BA. Sera and infecting isolates were collected from several patients with genital and disseminated gonococcal infections. Sera from two never-infected subjects and a hypogammaglobulinemic patient were also collected. Sera from patients with genital gonorrhea and never-infected controls demonstrated marked BA for gonococci after 30 min incubation. Chelation of these sera with MgEGTA delayed the expression of BA. Consumption of C3, but not C4, was observed in chelated samples. BA could not be demonstrated in any of the sera from DGI patients or the patient with hypogammaglobulinemia. Aliquots of fresh and chelated hypogammaglobulinemic serum to which IgM or IgG antigonococcal antibodies were added showed marked BA by 30 and 60 min, respectively. Absorption of chelated serum with a serum-sensitive isolate eliminated the previously observed delayed BA. The findings suggest that gonococcal serum BA is primarily associated with activation of the classic complement pathway. Activation of the alternate pathway also occurs; however, its expression is delayed and appears to be antibody-dependent.

摘要

为了更全面地了解宿主针对淋球菌感染的防御机制,我们决定确定经典补体途径和替代补体途径在淋球菌杀菌活性(BA)中的作用。从数名患有生殖器和播散性淋球菌感染的患者身上采集了血清和感染菌株。还采集了两名从未感染过的受试者以及一名低丙种球蛋白血症患者的血清。生殖器淋病患者和未感染对照的血清在孵育30分钟后对淋球菌显示出明显的杀菌活性。用MgEGTA螯合这些血清会延迟杀菌活性的表达。在螯合样本中观察到C3的消耗,但未观察到C4的消耗。在任何播散性淋球菌感染(DGI)患者或低丙种球蛋白血症患者的血清中均未显示出杀菌活性。分别向添加了IgM或IgG抗淋球菌抗体的新鲜和螯合的低丙种球蛋白血症血清等分试样中,在30分钟和60分钟时显示出明显的杀菌活性。用血清敏感菌株吸收螯合血清消除了先前观察到的延迟杀菌活性。这些发现表明,淋球菌血清杀菌活性主要与经典补体途径的激活有关。替代途径的激活也会发生;然而,其表达延迟,并且似乎是抗体依赖性的。

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