Indometacin farnesilのヒトB細胞免疫グロブリン産生に対する抑制作用  特にbucillamine・注射金剤との相互作用

DOI

書誌事項

タイトル別名
  • Inhibition of human B cell activation by indometacin farnesil: Its additive effects to the inhibitory influences of bucillamine or gold compounds.
  • <I>Its additive effects to the inhibitory influences of bucillamine or gold compounds</I>
  • ―特にbucillamine・注射金剤との相互作用―

抄録

Indometacin farnesil (IMF) is a prodrug of indomethacin (IND) designed to reduce the occurrence of side-effects by esterification of the carboxyl group on IND with farnesol (FAR) . Previous studies have shown that IMF has characteristics of disease modifying anti-rheumatic drug in that it has a component of slow acting effect in treatment of rheumatoid arthritis patients. We therefore examined the effects of IMF on human B cells. Ig production was induced from highly purified B cells obtained from healthy donors by stimulation with Staphylococcus aureus Cowan I (SA) plus IL-2. At pharmacologically attainable concentrations, IMF, but not IND, suppressed the production of IgM and IgG. Of note, IMF, but not IND, showed additive suppressive effects on the B cell Ig production in the presence of either intramolecular disulfide form of bucillamine (SA-981) or gold sodium thiomalate. FAR showed similar suppressive effects on B cells to those of IMF.<BR>These results indicate that IMF suppresses the human B cell functions by a different mechanism from that of bucillamine or gold sodium thiomalate. Thus, the data suggest that IMF may enhance the antirheumatic effects of bucillamine or gold sodium thiomalate.

収録刊行物

  • 炎症

    炎症 17 (6), 565-571, 1997

    日本炎症・再生医学会

詳細情報 詳細情報について

  • CRID
    1390001204785944832
  • NII論文ID
    130003709524
  • DOI
    10.2492/jsir1981.17.565
  • ISSN
    18844006
    03894290
  • 本文言語コード
    ja
  • データソース種別
    • JaLC
    • Crossref
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

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