Jiang X, Khursigara G, Rubin R L
W. M. Keck Autoimmune Disease Center, Department of Molecular and Experimental Medicine, Scripps Research Institute, La Jolla, CA 92037.
Science. 1994 Nov 4;266(5186):810-3. doi: 10.1126/science.7973636.
Drug-induced lupus is a serious side effect of certain medications, but the chemical features that confer this property and the underlying pathogenesis are puzzling. Prototypes of all six therapeutic classes of lupus-inducing drugs were highly cytotoxic only in the presence of activated neutrophils. Removal of extracellular hydrogen peroxide before, but not after, exposure of the drug to activated neutrophils prevented cytotoxicity. Neutrophil-dependent cytotoxicity required the enzymatic action of myeloperoxidase, resulting in the chemical transformation of the drug to a reactive product. The capacity of drugs to serve as myeloperoxidase substrates in vitro was associated with the ability to induce lupus in vivo.
药物性狼疮是某些药物的一种严重副作用,但赋予这种特性的化学特征及其潜在发病机制仍令人困惑。所有六类诱发狼疮药物的原型仅在存在活化中性粒细胞的情况下具有高度细胞毒性。在药物暴露于活化中性粒细胞之前而非之后去除细胞外过氧化氢可防止细胞毒性。中性粒细胞依赖性细胞毒性需要髓过氧化物酶的酶促作用,导致药物化学转化为反应性产物。药物在体外作为髓过氧化物酶底物的能力与在体内诱发狼疮的能力相关。