Ariza Adriana, Fernández-Santamaría Rubén, Meng Xiaoli, Salas María, Ogese Monday O, Tailor Arun, Bogas Gádor, Torres María José, Naisbitt Dean J
Allergy Research Group, Instituto de Investigación Biomédica de Málaga-IBIMA, Málaga, Spain.
Department of Molecular and Clinical Pharmacology, MRC Centre for Drug Safety Science, University of Liverpool, Liverpool, UK.
Allergy. 2020 Oct;75(10):2562-2573. doi: 10.1111/all.14298. Epub 2020 May 27.
Betalactam (BL) antibiotics are the most common cause of drug hypersensitivity. Amoxicillin (AX), which is often prescribed alongside clavulanic acid (Clav), is the most common elicitor. The aim of this study was to determine whether AX and Clav-responsive T-cells are detectable in patients with immediate hypersensitivity to AX-Clav, to assess whether these T-cells display the same specificity as that detected in skin and provocation testing, and to explore T-cell activation pathways.
Drug-specific T-cell clones were generated from immediate hypersensitive patients´ blood by serial dilution and repetitive mitogen stimulation. Antigen specificity was assessed by measurement of proliferation and cytokine release. CD4 /CD8 phenotype and chemokine receptor expression were analyzed by flow cytometry.
110 AX-specific and 96 Clav-specific T-cell clones were generated from seven patients with positive skin test to either AX or Clav. Proliferation of AX- and Clav-specific clones was dose-dependent, and no cross-reactivity was observed. AX- and Clav-specific clones required antigen-presenting cells to proliferate, and drugs were presented to CD4 and CD8 T-cells by MHC class-II and I, respectively. A higher secretion of IL-13 and IL-5 was detected in presence of the culprit drug compared with the alternative drug. Clones expressed CD69, CCR4, CXCR3, and CCR10.
Our study details the antigen specificity and phenotype of T-cell clones generated from patients with AX-Clav-induced immediate hypersensitivity diagnosed by positive skin test. AX- and Clav-specific clones were generated from patients irrespective of whether AX or Clav was the culprit, although differences in cytokine secretion were observed.
β-内酰胺(BL)类抗生素是药物超敏反应最常见的病因。常与克拉维酸(Clav)联合使用的阿莫西林(AX)是最常见的诱发因素。本研究的目的是确定在对AX-Clav立即发生超敏反应的患者中是否可检测到对AX和Clav有反应的T细胞,评估这些T细胞是否表现出与皮肤试验和激发试验中检测到的相同特异性,并探索T细胞激活途径。
通过系列稀释和重复丝裂原刺激,从立即发生超敏反应患者的血液中产生药物特异性T细胞克隆。通过测量增殖和细胞因子释放来评估抗原特异性。通过流式细胞术分析CD4/CD8表型和趋化因子受体表达。
从7例对AX或Clav皮肤试验呈阳性的患者中产生了110个AX特异性和96个Clav特异性T细胞克隆。AX和Clav特异性克隆的增殖呈剂量依赖性,未观察到交叉反应。AX和Clav特异性克隆需要抗原呈递细胞才能增殖,药物分别通过MHC-II类和I类呈递给CD4和CD8 T细胞。与替代药物相比,在有致病药物存在时检测到更高的IL-13和IL-5分泌。克隆表达CD69、CCR4、CXCR3和CCR10。
我们的研究详细描述了通过阳性皮肤试验诊断为AX-Clav诱导的立即超敏反应患者产生的T细胞克隆的抗原特异性和表型。无论AX还是Clav是致病因素,均从患者中产生了AX和Clav特异性克隆,尽管观察到细胞因子分泌存在差异。