Department of Molecular & Clinical Pharmacology, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool L69 3GE, UK.
Toxicol Sci. 2021 Aug 30;183(1):139-153. doi: 10.1093/toxsci/kfab084.
Drug rash with eosinophilia with systemic symptoms (DRESS) is a serious adverse event associated with use of the glycopeptide antibiotic vancomycin. Vancomycin-induced drug rash with eosinophilia with systemic symptoms is associated with the expression of human leukocyte antigen (HLA)-A32:01, suggesting that the drug interacts with this HLA to activate CD8+ T cells. The purpose of this study was to utilize peripheral blood mononuclear cell from healthy donors to: (1) investigate whether expression of HLA-A32:01 is critical for the priming naïve of T cells with vancomycin and (2) generate T-cell clones (TCC) to determine whether vancomycin exclusively activates CD8+ T cells and to define cellular phenotype, pathways of drug presentation and cross-reactivity. Dendritic cells were cultured with naïve T cells and vancomycin for 2 weeks. On day 14, cells were restimulated with vancomycin and T-cell proliferation was assessed by [3H]-thymidine incorporation. Vancomycin-specific TCC were generated by serial dilution and repetitive mitogen stimulation. Naïve T cells from HLA-A02:01 positive and negative donors were activated with vancomycin; however the strength of the induced response was significantly stronger in donors expressing HLA-A32:01. Vancomycin-responsive CD4+ and CD8+ TCC from HLA-A32:01+ donors expressed high levels of CXCR3 and CCR4, and secreted IFN-γ, IL-13, and cytolytic molecules. Activation of CD8+ TCC was HLA class I-restricted and dependent on a direct vancomycin HLA binding interaction with no requirement for processing. Several TCC displayed cross-reactivity with teicoplanin and daptomycin. To conclude, this study provides evidence that vancomycin primes naïve T cells from healthy donors expressing HLA-A32:01 through a direct pharmacological binding interaction. Cross-reactivity of CD8+ TCC with teicoplanin provides an explanation for the teicoplanin reactions observed in vancomycin hypersensitive patients.
药物超敏反应伴嗜酸性粒细胞增多和全身症状(DRESS)是一种严重的不良反应,与糖肽类抗生素万古霉素的使用有关。万古霉素诱导的药物超敏反应伴嗜酸性粒细胞增多和全身症状与人类白细胞抗原(HLA)-A32:01 的表达有关,表明该药物与该 HLA 相互作用以激活 CD8+T 细胞。本研究的目的是利用健康供者的外周血单核细胞:(1)研究 HLA-A32:01 的表达是否对用万古霉素对幼稚 T 细胞的启动至关重要;(2)生成 T 细胞克隆(TCC),以确定万古霉素是否仅激活 CD8+T 细胞,并确定细胞表型、药物呈递途径和交叉反应性。树突状细胞与幼稚 T 细胞和万古霉素共培养 2 周。第 14 天,用万古霉素再次刺激细胞,并通过[3H]-胸苷掺入评估 T 细胞增殖。通过连续稀释和重复有丝分裂原刺激生成万古霉素特异性 TCC。用万古霉素激活 HLA-A02:01 阳性和阴性供者的幼稚 T 细胞;然而,在表达 HLA-A32:01 的供者中,诱导反应的强度明显更强。来自 HLA-A32:01+供者的对万古霉素有反应的 CD4+和 CD8+TCC 表达高水平的 CXCR3 和 CCR4,并分泌 IFN-γ、IL-13 和细胞溶解分子。CD8+TCC 的激活受 HLA Ⅰ类限制,并且依赖于与 HLA 结合的万古霉素的直接相互作用,而无需加工。一些 TCC 与替考拉宁和达托霉素显示交叉反应性。总之,本研究提供了证据表明,万古霉素通过与 HLA-A32:01 的直接药理结合相互作用,从表达 HLA-A*32:01 的健康供者中启动幼稚 T 细胞。CD8+TCC 与替考拉宁的交叉反应性解释了在万古霉素超敏患者中观察到的替考拉宁反应。