Yoshizawa N, Oshima S, Takeuchi A, Kondo S, Oda T, Shimizu J, Nishiyama J, Ishida A, Nakabayashi I, Tazawa K, Sakurai Y
Department of Public Health, National Defence Medical College, Tokorozawa, Japan.
Clin Exp Immunol. 1997 Jan;107(1):61-7. doi: 10.1046/j.1365-2249.1997.d01-897.x.
FITC-labelled IgG obtained from patients convalescing from acute poststreptococcal glomerulonephritis (APSGN) stains glomeruli of patients with early APSGN. We previously reported a streptococcal antigen (preabsorbing antigen (PA-Ag)) that preabsorbed the stain out of sera from the convalescent patients and thus prevented glomerular staining. To confirm the nephritogenicity of PA-Ag, we administered up to 40 mg of this antigen to rabbits for 8 days and observed them for up to 9 weeks. Immunohistological analysis showed diffuse and global glomerular staining for C3 without notable staining for gamma-globulin. Light microscopic examinations revealed slight to moderate proliferative glomerulonephritis with exudative change. Control rabbits, which received similar doses of bovine serum albumin, did not show significant staining for C3. A transient and significant decrease in CH50 was observed from weeks 3 to 7 (9.7 +/- 0.3 U/ml at week 3; normal range 12.9 +/- 0.6 U/ml). This experimental model showed a resemblance to immunological and immunohistological features of APSGN in humans. Although the precise mechanisms are yet to be determined, complement activation by PA-Ag seems to hold a key position in this model and in the human disease.
从急性链球菌感染后肾小球肾炎(APSGN)恢复期患者获得的异硫氰酸荧光素标记的IgG可使早期APSGN患者的肾小球染色。我们之前报道过一种链球菌抗原(预吸收抗原(PA-Ag)),它能从恢复期患者的血清中去除染色,从而防止肾小球染色。为了证实PA-Ag的致肾炎性,我们给兔子注射高达40mg的这种抗原,持续8天,并对它们观察长达9周。免疫组织学分析显示C3呈弥漫性全肾小球染色,而γ-球蛋白无明显染色。光镜检查显示有轻度至中度增生性肾小球肾炎伴渗出性改变。接受相似剂量牛血清白蛋白的对照兔子,C3无明显染色。在第3至7周观察到CH50有短暂且显著的下降(第3周时为9.7±0.3U/ml;正常范围为12.9±0.6U/ml)。该实验模型显示出与人类APSGN的免疫学和免疫组织学特征相似。尽管确切机制尚待确定,但PA-Ag激活补体似乎在该模型和人类疾病中起着关键作用。