Kimura M, Mohri H, Shimada K, Wakabayashi T, Kanai Y, Matsuzawa A
Department of Internal Medicine, University of Tokyo, Japan.
Clin Exp Immunol. 1990 Jan;79(1):123-9. doi: 10.1111/j.1365-2249.1990.tb05138.x.
CBA/KlJms-lprcg/lprcg mice with a novel mutation producing systemic lymphoproliferation were investigated for their serological and histological characteristics. The mutant mice showed elevated levels of serum immunoglobulin, C1q-binding immune complexes and antibodies to nuclear antigens such as dsDNA and ssDNA and poly(ADP-ribose). In contrast, histopathological lesions, e.g. glomerulonephritis, vasculitis or interstitial pneumonitis, were not revealed by histological and immunofluorescent examinations, except for lymphocytic infiltration in various organs. These results suggest that this mutant mouse strain may provide a new animal model for autoimmunity. However, further investigations are required to clarify whether this strain is unique as compared with other well-known lupus-prone strains of mice with respect to serological and histological abnormalities and become to be a new model of systemic autoimmune disease.
对具有导致全身性淋巴细胞增殖的新突变的CBA/KlJms-lprcg/lprcg小鼠的血清学和组织学特征进行了研究。突变小鼠的血清免疫球蛋白、C1q结合免疫复合物以及针对核抗原(如双链DNA、单链DNA和聚(ADP-核糖))的抗体水平升高。相比之下,组织学和免疫荧光检查未发现组织病理学病变,如肾小球肾炎、血管炎或间质性肺炎,只是在各个器官中有淋巴细胞浸润。这些结果表明,这种突变小鼠品系可能为自身免疫提供一种新的动物模型。然而,需要进一步研究以阐明与其他著名的易患狼疮的小鼠品系相比,该品系在血清学和组织学异常方面是否独特,并成为系统性自身免疫疾病的新模型。