Coppo R, Mazzucco G, Martina G, Roccatello D, Amore A, Novara R, Bargoni A, Piccoli G, Sena L M
Department of Biomedical Sciences, University of Turin, Italy.
Lab Invest. 1989 Apr;60(4):499-506.
The effect of alimentary gluten and of its lectin-like fraction gliadin in inducing IgA mesangial deposits in BALB/c mice was investigated. In the pilot study G1 (4 mice), G2 (4 mice) and G3 (6 mice) received ovalbumin, human gamma-globulins, and crude gluten, respectively. The antigens, 1 mg/ml, were given in drinking water for 14 weeks. G4 (20 mice) were fed with standard mouse fodder. Gluten, as well as other alimentary antigens, induced IgA mesangial deposits with intense IgA staining in each animal, however a positive IgA staining was also observed in 10 of 20 adult controls. Antigliadin IgA antibodies were detected in renal tissue eluates from gluten-immunized mice but were found in eluates from control animals too. IgA deposits and antigliadin IgA in renal tissue were also observed in 3 of 7 adult mice (G7) fed for 30 weeks with standard fodder, then for 1 month with a protein-free diet supplemented with 20% amino acids. Conversely, there were no IgA mesangial deposits or IgA anti-gliadin antibodies in renal eluates of 1- or 2-week-old mice (G5 and G6). For the definitive protocol, 4-week-old BALB/c mice were selected and fed with basal glutenfree diet. G8 (14 mice) did not receive any alimentary immunogen in the drinking water, whereas G9 (15 mice) and G10 (15 mice) received ovalbumin and gliadin, respectively. G11 (15 mice) had standard gluten-containing diet. IgA deposits semiquantified by immunofluorescence scores were found to be significantly greater in G9 and G10 than in G8 (Student' t-test p1 less than 0.003, Mann-Whitney test p2 less than 0.001 and p1 less than 0.01, p2 less than 0.007, respectively), and in G11 than in G8 (p1 and p2 less than 0.05). The presence of positive IgA staining (greater than or equal to 2/6 scores) was significantly less frequent in G8 in comparison to G9 (chi-square test p3 less than 0.002), G10 (p3 less than 0.02) and G11 (p3 less than 0.04). Total serum IgA were significantly higher in orally immunized G9 and G10 than in G8 control mice (p1 less than 0.005, p2 less than 0.002). Anti-gliadin IgA in circulation as well as in renal deposit eluates were significantly increased in gluten-eating mice (G10 and G11) as compared with the gluten-free control group G8. These observations indicate that gliadin does induce IgA immune deposits in BALB/c mice.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了食物性谷蛋白及其类凝集素部分麦醇溶蛋白在诱导BALB/c小鼠IgA系膜沉积中的作用。在预实验中,G1组(4只小鼠)、G2组(4只小鼠)和G3组(6只小鼠)分别接受卵清蛋白、人γ球蛋白和粗谷蛋白。将浓度为1mg/ml的抗原加入饮用水中,持续给予14周。G4组(20只小鼠)喂食标准小鼠饲料。谷蛋白以及其他食物性抗原在每只动物中均诱导出IgA系膜沉积且IgA染色强烈,然而在20只成年对照小鼠中的10只也观察到了阳性IgA染色。在谷蛋白免疫小鼠的肾组织洗脱液中检测到了抗麦醇溶蛋白IgA抗体,但在对照动物的洗脱液中也发现了该抗体。在7只成年小鼠(G7组)中,3只小鼠先喂食30周标准饲料,然后喂食1个月补充20%氨基酸的无蛋白饮食,其肾组织中也观察到了IgA沉积和抗麦醇溶蛋白IgA。相反,1周龄或2周龄小鼠(G5和G6组)的肾洗脱液中未发现IgA系膜沉积或IgA抗麦醇溶蛋白抗体。在确定方案中,选择4周龄的BALB/c小鼠,喂食基础无谷蛋白饮食。G8组(14只小鼠)在饮用水中未接受任何食物性免疫原,而G9组(15只小鼠)和G10组(15只小鼠)分别接受卵清蛋白和麦醇溶蛋白。G11组(15只小鼠)给予标准含谷蛋白饮食。通过免疫荧光评分半定量的IgA沉积在G9组和G10组中显著高于G8组(学生t检验p1小于0.003,曼-惠特尼检验p2小于0.001且p1小于0.01,p2小于0.007),在G11组中高于G8组(p1和p2小于0.0