Van Pham T, Kreis B, Corradin-Betz S, Bauer J, Mauël J
Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.
J Biol Response Mod. 1990 Apr;9(2):231-40.
OM-89, a proteinaceous extract from Escherichia coli with very low endotoxin content, was tested for its capacity to stimulate in vitro cells involved in the immune response. OM-89 induced a marked proliferation of mouse spleen cells; E. coli lipopolysaccharide (LPS) at the same concentration as present in OM-89 was totally ineffective. Passage through nylon wool strongly decreased the OM-89-induced effect, suggesting that the responding lymphocytes were of the B lineage. Exposure of bone marrow-derived macrophages to OM-89 promoted glucose oxidation through the hexose monophosphate shunt pathway and the capacity to generate superoxide upon phorbol myristate acetate (PMA) stimulation. These effects were not blocked by polymyxin B, whereas this compound completely prevented induction of similar metabolic activation by E. coli lipopolysaccharide. In addition, OM-89 treatment induced marked PMA-dependent superoxide and hydrogen peroxide release by macrophages from the LPS low responder mouse strain C3H/HeJ. Incubation with recombinant murine interferon-gamma and OM-89, but not with either compound alone, led to functional activation, as shown by the killing of tumor target cells, and by the destruction of the intracellular parasite Leishmania enrietti by macrophages of both LPS-responsive and unresponsive mouse strains. These experiments indicate that OM-89 can stimulate metabolic and functional activities of lymphocytes and macrophages that are important for host defense.
OM-89是一种来自大肠杆菌的蛋白质提取物,内毒素含量极低,其刺激参与免疫反应的体外细胞的能力得到了测试。OM-89能显著诱导小鼠脾细胞增殖;与OM-89中相同浓度的大肠杆菌脂多糖(LPS)则完全无效。通过尼龙毛柱过滤后,OM-89诱导的效应显著降低,这表明产生反应的淋巴细胞属于B细胞系。将骨髓来源的巨噬细胞暴露于OM-89中,可通过磷酸己糖途径促进葡萄糖氧化,并增强在佛波酯(PMA)刺激下产生超氧化物的能力。这些效应不受多粘菌素B的阻断,而该化合物能完全抑制大肠杆菌脂多糖诱导的类似代谢激活。此外,OM-89处理可诱导LPS低反应性小鼠品系C3H/HeJ的巨噬细胞显著释放依赖PMA的超氧化物和过氧化氢。与重组鼠γ干扰素和OM-89共同孵育(而非单独使用任何一种化合物)可导致功能激活,这表现为对肿瘤靶细胞的杀伤,以及LPS反应性和无反应性小鼠品系的巨噬细胞对细胞内寄生虫恩氏利什曼原虫的破坏。这些实验表明,OM-89可刺激淋巴细胞和巨噬细胞的代谢及功能活动,而这些活动对宿主防御至关重要。