Bakker N P, van Erck M G, Botman C A, Jonker M, 't Hart B A
ITRI-TNO Primate Center, Rijswijk, The Netherlands.
Arthritis Rheum. 1991 May;34(5):616-24. doi: 10.1002/art.1780340514.
It is speculated that the autoimmune response to type II collagen (CII) is a driving force in the pathogenesis of human rheumatoid arthritis (RA). In this report, we describe the relationship between the induction of collagen arthritis and the CII-specific humoral, as well as cellular, immune response in rhesus monkeys. Ten of 14 monkeys immunized with bovine type II collagen (B-CII) developed polyarthritis. Susceptible animals showed a T cell response to B-CII; resistant animals did not. After the primary immunization, the humoral response to B-CII, as well as to rhesus monkey type II collagen, was dominated by antibodies of the IgM isotype in the susceptible animals and by antibodies of the IgG isotype in the resistant animals. Because of the close phylogenic relationship between the rhesus monkey and humans, these data contribute valuable information about the role of CII-specific immunity in the pathogenesis of human RA.
据推测,对II型胶原(CII)的自身免疫反应是人类类风湿性关节炎(RA)发病机制中的一个驱动力。在本报告中,我们描述了恒河猴胶原性关节炎的诱导与CII特异性体液免疫以及细胞免疫反应之间的关系。14只用牛II型胶原(B-CII)免疫的猴子中有10只发生了多关节炎。易感动物对B-CII表现出T细胞反应;抗性动物则没有。初次免疫后,易感动物对B-CII以及恒河猴II型胶原的体液反应以IgM同种型抗体为主,而抗性动物则以IgG同种型抗体为主。由于恒河猴与人类之间存在密切的系统发育关系,这些数据为CII特异性免疫在人类RA发病机制中的作用提供了有价值的信息。