Intranasal Administration of Denatured Type II Collagen and Its Fragments Can Delay the Onset of Collagen-Induced Arthritis

Takashi Matsumoto , Akio Ametani , Satoshi Hachimura , Amane Iwaya , Yasuki Taguchi , Kohtaro Fujita , Tamotsu Shigehisa , Shuichi Kaminogawa
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引用次数: 19

Abstract

Collagen-induced arthritis (CIA) is an autoimmune animal model for some types of human rheumatoid arthritis (RA). We have evaluated the effectiveness of intranasal administration of antigen in inhibiting CIA in DBA/1 mice. The intranasal administration of heat-denatured or trypsin-digested bovine type II collagen (CII) before immunization with CII strongly delayed the onset of CIA, whereas administration of native CII did not do so. The mice administered denatured or digested CII possessed much lower titers of anti-CII IgG2a than the control mice, whereas titers of anti-CII IgG1 and IgG2b were unchanged or slightly decreased. Responding to CII and peptides containing immunodominant T cell determinants, lymph node cells from mice administered denatured CII produced less IFN-gamma. These results suggest that intranasal administration of antigen downregulated preferentially Th1-type responses, whereas an enhanced Th2-type response was not observed. We demonstrate that the methods shown here are a possible treatment for rheumatoid arthritis.
鼻内给药变性II型胶原及其碎片可以延缓胶原诱导关节炎的发作
胶原诱导关节炎(CIA)是人类类风湿关节炎(RA)的一种自身免疫动物模型。我们已经评估了经鼻给药抗原抑制DBA/1小鼠CIA的有效性。在用CII免疫前,鼻内给予热变性或胰蛋白酶消化的牛II型胶原(CII),可显著延迟CIA的发生,而给予天然CII则没有这种作用。给予变性或消化的CII小鼠的抗CII IgG2a滴度远低于对照小鼠,而抗CII IgG1和IgG2b滴度不变或略有下降。对CII和含有免疫显性T细胞决定因子的肽作出反应,给予变性CII的小鼠淋巴结细胞产生较少的IFN-γ。这些结果表明,鼻内给药抗原优先下调th1型反应,而th2型反应没有增强。我们证明,这里显示的方法是一种可能的治疗类风湿关节炎。
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