Hahn B H, Knotts L L
Arthritis Rheum. 1979 Mar;22(3):236-42. doi: 10.1002/art.1780220305.
NZB/NZW F1 female mice received levamisole in an attempt to increase suppressor T cell function. Responses varied with dosage of drug and age of mice. When treatment with 25 microgram/gm doses (intermittent or daily) was begun at 12 weeks of age, nephritis was accelerated in spite of transient reduction of anti-DNA antibodies. When treatment was begun at 4 weeks, or when doses of 250 microgram/gm were given, no clinical effects were observed. In the mice with accelerated disease, delayed hypersensitivity and antibody responses to sheep erythrocytes increased; antibody responses to pneumococcal polysaccharide were unaffected. It is possible that some increased immune responses associated with levamisole are undesirable in murine lupus.
NZB/NZW F1雌性小鼠接受左旋咪唑以试图增强抑制性T细胞功能。反应随药物剂量和小鼠年龄而变化。当在12周龄开始用25微克/克剂量(间歇性或每日)治疗时,尽管抗DNA抗体短暂减少,但肾炎仍加速发展。当在4周龄开始治疗,或给予250微克/克剂量时,未观察到临床效果。在疾病加速发展的小鼠中,对绵羊红细胞的迟发型超敏反应和抗体反应增加;对肺炎球菌多糖的抗体反应未受影响。在小鼠狼疮中,一些与左旋咪唑相关的免疫反应增强可能是不良的。