普鲁卡因胺治疗患者和系统性红斑狼疮患者血清对Con A有丝分裂发生的抑制作用。

R H Tannen, S Cunningham-Rundles
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引用次数: 6

摘要

自发性系统性红斑狼疮患者或接受普鲁卡因胺治疗至少3个月的患者血清可特异性抑制普鲁卡因胺治疗患者或正常供者培养的外周血单个核细胞的Con A有丝分裂发生。将普鲁卡因胺治疗的患者转移到n -乙酰普鲁卡因胺可消除血清中的阻断因子。阻断因子不是普鲁卡因酰胺本身,因为将该药加入正常血清中,对正常外周血单核细胞有丝分裂仅有轻微影响。这些数据表明,系统性红斑狼疮和普鲁卡因酰胺诱导的狼疮在与Con a应答性外周血单核细胞(PBM)相关的调节缺陷的相对可逆性上可能不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of Con A mitogenesis by serum from procainamide-treated patients and patients with systemic lupus erythematosus.

Serum obtained from patients with spontaneous systemic lupus erythematosus or from patients treated at least 3 months with procainamide could specifically inhibit Con A mitogenesis of cultured peripheral blood mononuclear cells obtained from procainamide-treated patients or from normal donors. Transfer of procainamide treated patients to N-acetylprocainamide eliminated the blocking factor from their serum. The blocking factor is not procainamide itself since adding the drug to normal serum and only slight effects on mitogenesis of normal peripheral blood mononuclear cells. These data suggest that systemic lupus erythematosus and procainamide-induced lupus may differ in the relative reversibility of a regulatory defect associated with a Con A responsive population of peripheral blood mononuclear (PBM) cells.

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