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Oral feeding of renal tubular antigen abrogates interstitial nephritis and renal failure in Brown Norway rats

机译:口服饲喂肾小管抗原可消除挪威布朗大鼠的间质性肾炎和肾功能衰竭

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Oral feeding of renal tubular antigen abrogates interstitial nephritis and renal failure in Brown Norway rats. We have examined whether oral feeding of antigen can regulate the expression of autoimmune interstitial nephritis induced by antigen-in-adjuvant (RTA/CFA) immunization of Brown Norway rats. Male rats were divided into six experimental groups: Group I, RTA/CFA immunization alone; Groups II, III, and IV were pretreated with 1 mg (Group II), 5 mg (Group III), and 25 mg (Group IV) of oral tubular antigen every other day for ten days, followed by RTA/CFA immunization; Group V was pretreated with a control antigen, followed by RTA/CFA immunization; and Group VI was immunized with CFA alone. Renal histology, inulin clearance, DTH responses to RTA, and IgG antibody responses to RTA were monitored as endpoints of the study. Our results demonstrated that Group III and IV animals had significantly less severe renal injury, as assessed by inulin clearance and extent of renal cortical involvement by mononuclear cells. Group II and IV animals had suppressed DTH responses, and only Group IV animals had significantly depressed antigen-specific IgG serum titers. Group III animals had neither suppressed DTH responses or IgG titers. We conclude that oral administration of tubular antigen can modulate the intensity of interstitial nephritis produced by immunization, but that the regulatory mechanism is not dependent (at all doses of fed antigen) on suppressed DTH reactivity to RTA or suppressed antigen-specific IgG.
机译:口服饲喂肾小管抗原可消除布朗挪威大鼠的间质性肾炎和肾功能衰竭。我们检查了口服抗原是否可以调节布朗挪威大鼠佐剂抗原(RTA / CFA)免疫诱导的自身免疫性间质性肾炎的表达。将雄性大鼠分为六个实验组:第一组,单独进行RTA / CFA免疫; II,III和IV组每隔一天用1 mg(II组),5 mg(III组)和25 mg(IV组)口服小管抗原预处理10天,然后进行RTA / CFA免疫。 V组用对照抗原预处理,然后进行RTA / CFA免疫;第六组仅用CFA免疫。监测肾脏组织学,菊粉清除率,对RTA的DTH反应和对RTA的IgG抗体反应作为研究的终点。我们的结果表明,通过菊粉清除率和单核细胞对肾皮质的侵袭程度评估,第三组和第四组动物的肾损伤明显较少。 II组和IV组动物抑制了DTH反应,只有IV组动物具有显着降低的抗原特异性IgG血清滴度。第三组动物均未抑制DTH反应或IgG效价。我们得出的结论是,口服肾小管抗原可以调节免疫接种所产生的间质性肾炎的强度,但是调节机制并不依赖于DTH对RTA的反应性或抗原特异性IgG的抑制(在所有剂量的饲喂抗原中)。

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