期刊
ALLERGY
卷 75, 期 10, 页码 2562-2573出版社
WILEY
DOI: 10.1111/all.14298
关键词
amoxicillin; clavulanic acid; immediate hypersensitivity; phenotype; T-cell
资金
- Institute of Health Carlos III (ISCIII) of the Ministry of Economy and Competitiveness [PI12/02529, PI15/01206]
- Institute of Health Carlos III (ISCIII) of the Ministry of Economy and Competitiveness: RETICS ARADyAL [RD16/0006/0001, RD16/0006/0021]
- Institute of Health Carlos III (ISCIII) of the Ministry of Economy and Competitiveness: Biobank platform [PT13/0010/0006, PT17/0015/0041]
- Andalusian Regional Ministry of Health [PI-0699-2011, PI-0179-2014, PI-0241-2016]
- Merck-Serono Research Grant from Fundacion Salud 2000
- Andalucia Talent Hub Fellowship Program [TAHUB/II-004]
- Junta de Andalucia
- European Commission, European Union's VII Framework Programme for Research, Technological Development and Demonstration [291780]
- BBSRC [BB/R008108/1]
- MRC [MR/R009635/1]
- ISCIII [JR18/00054]
- European Social Fund
- European Regional Development Fund
- BBSRC [BB/R008108/1] Funding Source: UKRI
- MRC [MR/R009635/1] Funding Source: UKRI
Background 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. Methods 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. Results 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. Conclusions 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.
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