Manoury-Schwartz B, Chiocchia G, Bessis N, Abehsira-Amar O, Batteux F, Muller S, Huang S, Boissier M C, Fournier C
National Institute of Health and Medical Research (INSERM), Unit 283, René Descartes University, Paris, France.
J Immunol. 1997 Jun 1;158(11):5501-6.
Collagen-induced arthritis (CIA), an animal model for rheumatoid arthritis, is induced in DBA/1 (H-2q) mice following immunization with type II collagen (CII) in CFA. Since we have previously shown that IFN-gamma exerts a biphasic effect during the evolution of CIA in DBA/1 mice, we analyzed the development of this disease in mice with a disruption of the IFN-gamma receptor gene (IFN-gammaR(0/0)). Mutant mice were interbred with the DBA/1 strain to yield IFN-gammaR(0/0) mice expressing the H-2q haplotype. In three consecutive experiments, IFN-gammaR(0/0) male mice were found to exhibit severe clinical and histologic arthritis with an average incidence of 88.5 vs 94.1% for the wild DBA/1 strain. Notably, onset of clinical symptoms occurred significantly earlier than in DBA/1 mice. Although of a lower magnitude than in males, CIA also developed early in IFN-gammaR(0/0) female mice and with higher clinical severity than in control DBA/1 females. Immunization of knockout mice with CII resulted in the generation of CII-specific T cells belonging to the Th1 phenotype that recognize the same immunodominant peptides as do DBA/1 mice. CIA in IFN-gammaR(0/0) mice was associated with a down-regulation of the CII-specific IgG response, and this impairment was essentially due to a strong reduction of Abs of the IgG2a isotype. Taken together, our findings provide evidence that IFN-gammaR deficiency in DBA/1 mice leads to the occurrence of severe CIA with an accelerated onset compared with that in wild-type mice, indicating that the proinflammatory action of IFN-gamma has been bypassed in the IFN-gammaR(0/0) mice.
胶原诱导性关节炎(CIA)是类风湿性关节炎的一种动物模型,在用完全弗氏佐剂(CFA)中的II型胶原(CII)免疫后,DBA/1(H-2q)小鼠会诱发该疾病。由于我们之前已经表明,在DBA/1小鼠的CIA病程中,干扰素-γ发挥双相作用,因此我们分析了干扰素-γ受体基因(IFN-γR(0/0))缺失小鼠中这种疾病的发展情况。将突变小鼠与DBA/1品系杂交,以产生表达H-2q单倍型的IFN-γR(0/0)小鼠。在连续三个实验中,发现IFN-γR(0/0)雄性小鼠表现出严重的临床和组织学关节炎,平均发病率为88.5%,而野生DBA/1品系为94.1%。值得注意的是,临床症状的发作明显早于DBA/1小鼠。虽然程度低于雄性,但CIA在IFN-γR(0/0)雌性小鼠中也较早出现,且临床严重程度高于对照DBA/1雌性小鼠。用CII免疫敲除小鼠会产生属于Th1表型的CII特异性T细胞,这些T细胞识别与DBA/1小鼠相同的免疫显性肽。IFN-γR(0/0)小鼠中的CIA与CII特异性IgG反应的下调有关,这种损害主要是由于IgG2a同种型抗体的强烈减少。综上所述,我们的研究结果表明,DBA/1小鼠中的IFN-γR缺陷导致严重CIA的发生,与野生型小鼠相比发病加速,这表明在IFN-γR(0/0)小鼠中,干扰素-γ的促炎作用被绕过了。