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对MRL/1小鼠长期给予环磷酰胺。II. 对脾脏中抗DNA抗体的同种型及免疫球蛋白分泌细胞的影响。

Long term administration of cyclophosphamide into MRL/1 mice. II. The effects on the isotype of anti-DNA antibodies and immunoglobulin secreting cells in the spleen.

作者信息

Shiraki M, Fujiwara M

出版信息

Clin Exp Immunol. 1984 Mar;55(3):519-24.

Abstract

Weekly injections of cyclophosphamide (Cy) at a dose of 20 mg/kg body weight prevented IgM to IgG class switch of serum anti-DNA antibodies and also immunoglobulin secreting cells in the spleen of MRL/Mp-lpr/lpr (MRL/1) mice. Culture experiments revealed that splenic B cells of Cy treated mice gave rise to more IgM and less IgG secreting cells than those of untreated mice in response to lipopolysaccharide. These results suggested that Cy suppressed enhanced differentiation of B cells into IgG secreting cells in MRL/1 mice, which would result in reduction of IgG anti-single stranded DNA antibodies and improvement of murine lupus like syndrome.

摘要

每周以20毫克/千克体重的剂量注射环磷酰胺(Cy)可防止MRL/Mp-lpr/lpr(MRL/1)小鼠血清抗DNA抗体的IgM向IgG类别转换,也可防止脾脏中免疫球蛋白分泌细胞的转换。培养实验表明,与未处理小鼠相比,经Cy处理的小鼠的脾脏B细胞在对脂多糖的反应中产生更多分泌IgM的细胞和更少分泌IgG的细胞。这些结果表明,Cy抑制了MRL/1小鼠中B细胞向分泌IgG细胞的增强分化,这将导致IgG抗单链DNA抗体减少,并改善小鼠狼疮样综合征。

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