Department of Endocrinology, The Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Medical Inflammation Research, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm, Sweden.
Front Immunol. 2021 Feb 23;12:631249. doi: 10.3389/fimmu.2021.631249. eCollection 2021.
The most commonly used strains in experimental research, including genetically modified strains, are C57BL/6 mice. However, so far, no reliable model for rheumatoid arthritis is available, mainly due to the restriction by the MHC class II haplotype H-2. Collagen-induced arthritis (CIA) is the most widely used animal model of rheumatoid arthritis, but C57BL/6 strain is resistant to CIA because there is no collagen II peptide associated with H-2. To establish a rheumatoid arthritis model in C57BL/6 mice, we immunized C57BL/6NJ (B6N) mice with human cartilage oligomeric matrix protein (COMP), which induced severe arthritis with high incidence, accompanied by a strong auto-antibody response. Native COMP was required, as denatured COMP lost its ability to induce arthritis in B6N mice. An immunodominant COMP peptide was identified as the key T cell epitope, with a perfect fit into the A class II peptide binding pocket. A critical amino acid in this peptide was found to be phenylalanine at position 95. Recombinant COMP mutated at position 95 (COMP_F95S) lost its ability to induce arthritis or a strong immune response in the B6N mice. In conclusion, A new model for RA has been established using C57BL/6 mice through immunization with COMP, which is dependent on a COMP specific peptide binding A, thus in similarity with CIA in A expressing strains.
最常用于实验研究的菌株,包括基因修饰菌株,是 C57BL/6 小鼠。然而,到目前为止,还没有可靠的类风湿关节炎模型,主要是由于 MHC Ⅱ类单倍型 H-2 的限制。胶原诱导关节炎(CIA)是最广泛应用的类风湿关节炎动物模型,但 C57BL/6 品系对 CIA 有抗性,因为没有与 H-2 相关的胶原 II 肽。为了在 C57BL/6 小鼠中建立类风湿关节炎模型,我们用软骨寡聚基质蛋白(COMP)免疫 C57BL/6NJ(B6N)小鼠,诱导出高发病率的严重关节炎,并伴有强烈的自身抗体反应。天然 COMP 是必需的,因为变性 COMP 丧失了在 B6N 小鼠中诱导关节炎的能力。鉴定出一个免疫优势 COMP 肽是关键的 T 细胞表位,与 A 类 II 肽结合口袋完美匹配。该肽中的一个关键氨基酸是位置 95 的苯丙氨酸。位置 95 突变的重组 COMP(COMP_F95S)丧失了在 B6N 小鼠中诱导关节炎或强烈免疫反应的能力。总之,通过用 COMP 免疫 C57BL/6 小鼠建立了一种新的 RA 模型,该模型依赖于 COMP 特异性肽结合 A,因此与 A 表达品系中的 CIA 相似。