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The effect of a new antirheumatic drug, triethylphosphine gold (auranofin), on in vitro lymphocyte and monocyte cytotoxicity.

作者信息

Russell A S, Davis P, Miller C

出版信息

J Rheumatol. 1982 Jan-Feb;9(1):30-5.

PMID:6806471
Abstract

Therapeutic serum concentrations of auranofin, expressed as elemental gold, range from 0.25 - 1.0 micrograms/ml. Monocyte antibody dependent cellular cytotoxicity (ADCC) could be reduced by up to 50% at a gold concentration of 0.125 micrograms/ml. Lymphocyte ADCC was much less dramatically affected although 2.5 micrograms/ml produced virtually complete inhibition. The most surprising finding is a marked stimulation of natural killer (NK) cell activity using a variety of targets. NK activity was markedly enhanced by concentrations of 0.125 to 0.5 micrograms/ml (range 2-500%). This is a biphasic dose dependent response. 1.0 micrograms/ml was depressive and 2.5 micrograms/ml completely abolished NK cell activity. Whether these selected in vitro responses play a role in modulating tissue damage in vivo is yet to be determined.

摘要

相似文献

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引用本文的文献

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Auranofin. A preliminary review of its pharmacological properties and therapeutic use in rheumatoid arthritis.金诺芬。其药理特性及在类风湿性关节炎治疗中的应用的初步综述。
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3
A comparison of the effects of two gold-containing therapeutic agents on articular chondrocyte growth in vitro.两种含金治疗剂对体外关节软骨细胞生长影响的比较。
Rheumatol Int. 1983;3(2):49-56. doi: 10.1007/BF00541144.
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In vitro boost of human NK activity by a triethylphosphine gold derivative.三乙膦金衍生物对人自然杀伤细胞活性的体外增强作用。
Clin Exp Immunol. 1984 Jul;57(1):207-10.