Smith S R, Terminelli C, Kipilman C T, Smith Y
Shering Corporation, Department of Physiology, Bloomfield, New Jersey 07003.
J Immunopharmacol. 1979;1(4):455-81. doi: 10.3109/08923977909040546.
Data is presented comparing the activities of three immunosuppressive agents, cyclosphosphamide, frentizole and azathioprine in models of humoral immunity in mice. Cyclophosphamide and frentizole suppressed the primary and secondary plaque forming cell responses to sheep erythrocytes at lower doses than did azathioprine. Prolonged suppression of serum antibody titers occurred following short-term therapy with cyclophosphamide or frentizole, but not azathioprine. Azathioprine was also the least effective agent in suppressing a primary response to the T-independent antigen, trinitrophenylated lipopolysaccharide. All three agents were found to inhibit the induction and activity of suppressor cells at immunosuppressive doses.
本文呈现了在小鼠体液免疫模型中比较三种免疫抑制剂(环磷酰胺、氟仑替唑和硫唑嘌呤)活性的数据。与硫唑嘌呤相比,环磷酰胺和氟仑替唑在更低剂量时就能抑制对绵羊红细胞的初次和二次斑块形成细胞反应。用环磷酰胺或氟仑替唑进行短期治疗后,血清抗体滴度出现了长期抑制,但硫唑嘌呤没有。硫唑嘌呤在抑制对非T细胞依赖性抗原三硝基苯基化脂多糖的初次反应方面也是效果最差的药物。发现所有三种药物在免疫抑制剂量下均能抑制抑制性细胞的诱导和活性。