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一种链球菌抗原在急性链球菌感染后肾小球肾炎发病机制中的作用。该抗原的特性及疾病的一种推测机制。

Role of a streptococcal antigen in the pathogenesis of acute poststreptococcal glomerulonephritis. Characterization of the antigen and a proposed mechanism for the disease.

作者信息

Yoshizawa N, Oshima S, Sagel I, Shimizu J, Treser G

机构信息

Second Department of Medicine, National Defense Medical College, Tokorozawa, Japan.

出版信息

J Immunol. 1992 May 15;148(10):3110-6.

PMID:1578137
Abstract

We studied the significance of a streptococcal protein (preabsorbing Ag) (PA-Ag) in the pathogenesis of acute poststreptococcal glomerulonephritis (APSGN). This protein was isolated from nephritogenic streptococci. Purification of PA-Ag was achieved by chromatography, followed by Sephadex IEF. A single protein band at pH 4.7 was identified as PA-Ag. The m.w. was 43,000. Rabbit antisera against PA-Ag and sera of patients with APSGN showed identical precipitation lines by immunodiffusion. Antibodies to PA-Ag were found to be present in 30 of 31 patients with APSGN, in 1 of 36 patients with uncomplicated group A streptococcal upper respiratory tract infections, and in 1 of 36 normal adults. By using immunoelectrophoresis, it was found that PA-Ag activates the alternate pathway of C. Other water-soluble streptococcal fractions, used as controls, did not activate the C system. The demonstration that PA-Ag is present in the glomeruli in the early phase of APSGN and its ability to activate C3 and factor B suggest that PA-Ag may be involved in the pathogenesis of APSGN, via in situ C activation.

摘要

我们研究了一种链球菌蛋白(预吸附抗原)(PA-Ag)在急性链球菌感染后肾小球肾炎(APSGN)发病机制中的意义。这种蛋白是从致肾炎性链球菌中分离出来的。PA-Ag通过层析法进行纯化,随后进行Sephadex等电聚焦。在pH 4.7处的单一蛋白条带被鉴定为PA-Ag。其分子量为43,000。抗PA-Ag的兔抗血清与APSGN患者的血清在免疫扩散试验中显示出相同的沉淀线。在31例APSGN患者中有30例、36例无并发症的A组链球菌上呼吸道感染患者中有1例以及36例正常成年人中有1例检测到抗PA-Ag抗体。通过免疫电泳发现,PA-Ag激活补体的替代途径。用作对照的其他水溶性链球菌组分未激活补体系统。PA-Ag在APSGN早期存在于肾小球中,并且具有激活C3和B因子的能力,这表明PA-Ag可能通过原位补体激活参与APSGN的发病机制。

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