Ito S, Ueno M, Arakawa M, Saito T, Aoyagi T, Fujiwara M
Department of Medicine II, Niigata University School of Medicine, Japan.
Clin Exp Immunol. 1990 Sep;81(3):446-53. doi: 10.1111/j.1365-2249.1990.tb05354.x.
The effect of 15-deoxyspergualin (DSP), a newly developed immunosuppressive agent, on the development of spontaneously occurring lupus glomerulonephritis in MRL-lpr mice was examined. Administration of the drug was initiated at the age of 13 or 17 weeks, when polyclonal B cell activation and lupus nephropathy were apparent or became prominent. Treatment with DSP for up to 19 weeks of age at a dose of 2 mg/kg twice a day or 5 mg/kg daily strongly suppressed the increment of IgG-producing cell numbers in the spleen and serum levels of immune complexes and anti-DNA antibodies. Glomerular histological score estimated by light microscopy and IgG and C3 deposition in renal glomeruli were improved, compared with untreated control mice. Thus, DSP was shown to suppress the progression of polyclonal B cell activation and lupus nephropathy in MRL/lpr mice. These results suggest that DSP may be used as a therapeutic agent for systemic lupus erythematosus.
研究了新开发的免疫抑制剂15-脱氧精胍菌素(DSP)对MRL-lpr小鼠自发性狼疮性肾小球肾炎发展的影响。在13或17周龄时开始给药,此时多克隆B细胞活化和狼疮性肾病明显或变得突出。以2mg/kg的剂量每天两次或5mg/kg的剂量每天对DSP进行治疗,直至19周龄,强烈抑制了脾脏中产生IgG的细胞数量的增加以及免疫复合物和抗DNA抗体的血清水平。与未治疗的对照小鼠相比,通过光学显微镜估计的肾小球组织学评分以及肾小球中IgG和C3的沉积得到改善。因此,DSP被证明可抑制MRL/lpr小鼠多克隆B细胞活化和狼疮性肾病的进展。这些结果表明,DSP可能用作系统性红斑狼疮的治疗剂。