Walker S E, Schnitzer B
Arthritis Rheum. 1980 May;23(5):539-44. doi: 10.1002/art.1780230504.
Inbred Palmerston North (PN) mice are a newly recognized model of systemic lupus erythematosus. In this study PN mice with established autoimmune disease were treated until death with cyclophosphamide (8 mg/kg/day) or hydrocortisone (10 mg/kg/day). These doses had previously been found to prevent or suppress disease in another lupus model, the NZB/NZW mouse. In the PN strain, autoantibodies, severity of glomerulonephritis, and longevity were not influenced by treatment. Furthermore, the incidence of neoplasms was not increased in PN mice receiving prolonged therapy with immunosuppressive drugs. Unlike NZB/NZW mice, PN mice were resistant to the effects of Cyclophosphamide and hydrocortisone.
近交系帕尔默斯顿北(PN)小鼠是一种新发现的系统性红斑狼疮模型。在本研究中,已患自身免疫性疾病的PN小鼠接受环磷酰胺(8毫克/千克/天)或氢化可的松(10毫克/千克/天)治疗直至死亡。这些剂量此前已被发现可预防或抑制另一种狼疮模型——新西兰黑/新西兰白(NZB/NZW)小鼠的疾病。在PN品系中,自身抗体、肾小球肾炎的严重程度和寿命均不受治疗影响。此外,接受免疫抑制药物长期治疗的PN小鼠肿瘤发生率并未增加。与NZB/NZW小鼠不同,PN小鼠对环磷酰胺和氢化可的松的作用具有抗性。