MRC Centre for Drug Safety Science, Department of Pharmacology, University of Liverpool, Sherrington Building, Ashton Street, Liverpool, L69 3GE, England.
Chem Res Toxicol. 2011 Jun 20;24(6):791-3. doi: 10.1021/tx2001256. Epub 2011 May 3.
Pathways of drug-specific T-cell stimulation have not been fully defined. The aim of this study was to use T-cell clones from a patient hypersensitive to the drug trimethoprim to characterize the involvement of drug metabolism and processing in antigen presentation and cross-reactivity patterns. The MHC-restricted CD4+ and CD8+ T-cell response was dependent on the presence of antigen-presenting cells, and both processing-dependent and -independent pathways of antigen presentation were detected. Stimulation of certain clones was blocked through inhibition of drug-metabolizing enzyme activity. Trimethoprim clones were additionally stimulated with diaveridine and pyrimethamine but not other closely related structures.
药物特异性 T 细胞刺激的途径尚未完全确定。本研究的目的是使用对药物甲氧苄啶过敏的患者的 T 细胞克隆来描述药物代谢和处理在抗原呈递和交叉反应模式中的参与情况。MHC 限制性 CD4+和 CD8+T 细胞反应依赖于抗原呈递细胞的存在,并且检测到了依赖和不依赖于处理的抗原呈递途径。通过抑制药物代谢酶的活性,阻断了某些克隆的刺激。二甲氧苄啶和乙胺嘧啶还可刺激甲氧苄啶克隆,但不能刺激其他密切相关的结构。