Giampietri A, Puccetti P, Contessa A R
J Immunopharmacol. 1981;3(2):251-64. doi: 10.3109/08923978109026430.
Administration of BCG and Corynebacterium parvum is known to cause depression of the hepatic microsomal enzyme system (HMES) in mice. In the present study we explored the effects on HMES of two chemical immunoadjuvants, one of which (pyran copolymer) with peculiarly long-lasting biological activities. The two synthetic immunoadjuvants proved to be potent HMES inhibitors and, for pyran copolymer, peak levels of inhibition concurred with maximal macrophage activation. The inhibition was largely dose-dependent and could not be prevented by immunopharmacologic maneuvers that are known to block the C. parvum effect on HMES. The possibility is discussed that common mechanism(s) underlie the depression of HMES by immunoactive substances of both bacterial and chemical origin.
已知接种卡介苗(BCG)和短小棒状杆菌会导致小鼠肝脏微粒体酶系统(HMES)受到抑制。在本研究中,我们探究了两种化学免疫佐剂对HMES的影响,其中一种(聚吡喃共聚物)具有特别持久的生物活性。这两种合成免疫佐剂被证明是强效的HMES抑制剂,对于聚吡喃共聚物而言,抑制的峰值水平与巨噬细胞的最大激活同时出现。这种抑制在很大程度上是剂量依赖性的,并且已知能阻断短小棒状杆菌对HMES作用的免疫药理操作无法预防这种抑制。本文讨论了细菌和化学来源的免疫活性物质导致HMES抑制的共同机制的可能性。