Mayus J L, Semper K F, Pisetsky D S
Cell Immunol. 1985 Aug;94(1):195-204. doi: 10.1016/0008-8749(85)90096-6.
The action of the immunosuppressive agent cyclosporine (CsA) on anti-DNA B-cell responses was investigated in an in vitro system. Spleen cells from autoimmune MRL-lpr/lpr or control BALB/c mice, when cultured at high cell density, spontaneously produced significant amounts of IgM and IgG, including anti-DNA. IgG levels, both total and anti-DNA, were much higher for MRL-lpr/lpr cells compared to BALB/c cells, suggesting similarity of this model system to the in vivo response. For cells of both strains, the production of IgM and IgG anti-DNA was 10- to 100-fold more sensitive to the inhibitory activity of CsA than total immunoglobulin production. The effect was not manifest, however, in cultures stimulated with the B-cell mitogen, lipopolysaccharide. These observations suggest that CsA in certain dose ranges preferentially inhibits anti-DNA production, with efficacy determined by the mechanisms promoting B-cell hyperactivity.
在体外系统中研究了免疫抑制剂环孢素(CsA)对抗DNA B细胞反应的作用。来自自身免疫性MRL-lpr/lpr小鼠或对照BALB/c小鼠的脾细胞,在高细胞密度培养时,会自发产生大量的IgM和IgG,包括抗DNA抗体。与BALB/c细胞相比,MRL-lpr/lpr细胞的总IgG水平和抗DNA IgG水平要高得多,这表明该模型系统与体内反应相似。对于这两种品系的细胞,IgM和IgG抗DNA的产生对CsA抑制活性的敏感性比对总免疫球蛋白产生的敏感性高10到100倍。然而,在用B细胞有丝分裂原脂多糖刺激的培养物中,这种作用并不明显。这些观察结果表明,在某些剂量范围内,CsA优先抑制抗DNA的产生,其疗效取决于促进B细胞过度活跃的机制。