Cheema A, Henson J B, Gorham J R
Am J Pathol. 1972 Mar;66(3):543-56.
Mink that were homozygous recessive for the Aleutian gene (aa) were inoculated with Aleutian disease virus (ADV) and simultaneously treated with cyclophosphamide (Cy). Control mink were inoculated with ADV. All mink were injected with bovine serum albumin (BSA) and their anti-BSA antibody response was measured to monitor the influence of drug therapy on the humoral antibody response. Formation of anti-BSA antibody was markedly suppressed and the hypergammaglobulinemia and development of AD lesions was inhibited in the Cy-treated mink. The non-Cy-treated control mink developed characteristic signs and lesions including glomerulonephritis and arteritis. The nontreated ADV-infected mink, but not the Cy-treated ADV-infected mink, had glomerular deposition of C3 and gamma globulin. Both groups had high titers of virus in their blood. These results indicate that the development of ADV lesions can be prevented by immunosuppressive treatment and further implicate host immune mechanisms in the pathogenesis of Aleutian disease.
对阿留申基因(aa)呈纯合隐性的水貂接种阿留申病病毒(ADV),并同时用环磷酰胺(Cy)进行治疗。对照水貂接种ADV。所有水貂均注射牛血清白蛋白(BSA),并检测其抗BSA抗体反应,以监测药物治疗对体液抗体反应的影响。在经Cy治疗的水貂中,抗BSA抗体的形成明显受到抑制,高球蛋白血症和AD病变的发展也受到抑制。未经Cy治疗的对照水貂出现了包括肾小球肾炎和动脉炎在内的特征性症状和病变。未治疗的ADV感染水貂,但经Cy治疗的ADV感染水貂没有,出现了C3和γ球蛋白在肾小球的沉积。两组水貂血液中的病毒滴度都很高。这些结果表明,免疫抑制治疗可以预防ADV病变的发展,并进一步表明宿主免疫机制在阿留申病发病机制中的作用。