Masihi K N, Brehmer W, Lange W, Ribi E, Schwartzman S
J Biol Response Mod. 1984 Dec;3(6):663-71.
The effects of two aminobutyryl and four seryl analogs of the synthetic muramyl dipeptide (MDP) against aerosol infections with influenza virus and Mycobacterium tuberculosis were studied. Regardless of the MDP analog employed, there was no evidence that the resistance against viral and bacterial aerosol infections was enhanced in the treated mice. In parallel studies, significant protection against influenza virus and M. tuberculosis infections was induced by the combination of MDP or analogs with the mycobacterial glycolipid trehalose dimycolate (TDM). Resistance conferred by the MDP + TDM combination against influenza virus was present 1 week after pretreatment and could be abrogated by macrophage inhibitory agents silica, dextran sulfate, and carrageenan. Splenic cells from MDP + TDM-pretreated animals generated markedly enhanced levels of luminol-dependent chemiluminescence in response to influenza A and B viruses.
研究了合成的胞壁酰二肽(MDP)的两种氨基丁酰类似物和四种丝氨酰类似物对流感病毒和气溶胶感染结核分枝杆菌的影响。无论使用哪种MDP类似物,均没有证据表明经治疗的小鼠对病毒和细菌气溶胶感染的抵抗力增强。在平行研究中,MDP或其类似物与分枝杆菌糖脂海藻糖二霉菌酸酯(TDM)联合使用可诱导对流感病毒和结核分枝杆菌感染的显著保护作用。MDP + TDM组合赋予的抗流感病毒能力在预处理1周后出现,并且可被巨噬细胞抑制剂二氧化硅、硫酸葡聚糖和角叉菜胶消除。来自MDP + TDM预处理动物的脾细胞在对甲型和乙型流感病毒的反应中产生明显增强的鲁米诺依赖性化学发光水平。