Bakker N P, van Erck M G, Otting N, Lardy N M, Noort R C, 't Hart B A, Jonker M, Bontrop R E
Institute for Applied Radiobiology and Immunology, Rijswijk, The Netherlands.
J Exp Med. 1992 Apr 1;175(4):933-7. doi: 10.1084/jem.175.4.933.
Type II collagen-induced arthritis (CIA) is an experimentally inducible autoimmune disorder that is, just like several forms of human arthritis, influenced by a genetic background. Immunization of young rhesus monkeys (Macaca mulatta) with type II collagen (CII) induced CIA in about 70% of the animals. One major histocompatibility complex (MHC) class I allele was present only in young animals resistant to CIA and absent in arthritic animals. This strong association suggests that the MHC class I allele itself, or a closely linked gene, determines resistance to CIA. The mechanism controlling the resistance to CIA becomes less efficient in aged animals since older rhesus monkeys, which were positive for the resistance marker, developed a mild form of arthritis. At the cellular level it is demonstrated that resistance to CIA is reflected by a low responsiveness of T cells to CII. This association between a specified MHC class I allele and resistance to an autoimmune disease points at the importance of the MHC class I region in the regulation of the immune response to an autoantigen.
II型胶原诱导的关节炎(CIA)是一种实验性诱导的自身免疫性疾病,与几种人类关节炎形式一样,受遗传背景影响。用II型胶原(CII)免疫幼年恒河猴(猕猴)可在约70%的动物中诱导出CIA。一个主要组织相容性复合体(MHC)I类等位基因仅存在于对CIA有抗性的幼年动物中,而在患关节炎的动物中不存在。这种强关联表明,MHC I类等位基因本身或紧密连锁的基因决定了对CIA的抗性。由于对CIA抗性的控制机制在老年动物中效率降低,因为对抗性标记呈阳性的老年恒河猴会发展出轻度关节炎。在细胞水平上表明,对CIA的抗性表现为T细胞对CII的低反应性。特定的MHC I类等位基因与自身免疫性疾病抗性之间的这种关联表明MHC I类区域在调节对自身抗原的免疫反应中的重要性。