Publication:
Hypersensitivity to fluoroquinolones: The expression of basophil activation markers depends on the clinical entity and the culprit fluoroquinolone.

dc.contributor.authorFernández, Tahia D
dc.contributor.authorAriza, Adriana
dc.contributor.authorPalomares, Francisca
dc.contributor.authorMontañez, María I
dc.contributor.authorSalas, María
dc.contributor.authorMartín-Serrano, Angela
dc.contributor.authorFernández, Rubén
dc.contributor.authorRuiz, Arturo
dc.contributor.authorBlanca, Miguel
dc.contributor.authorMayorga, Cristobalina
dc.contributor.authorTorres, María J
dc.date.accessioned2023-01-25T08:33:15Z
dc.date.available2023-01-25T08:33:15Z
dc.date.issued2016
dc.description.abstractAlthough fluoroquinolones (FQs) are generally well-tolerated antibiotics, increasing numbers of hypersensitivity reactions have been reported. These can be evaluated in vitro by basophil activation tests (BATs); however, sensitivity is not optimal. Many factors could influence sensitivity such as basophil activation markers. The objective of this study was to evaluate the influence of 2 different activations markers, CD63 and CD203c, on the sensitivity of BAT to FQ. We studied 17 patients with immediate allergic reactions to FQ. BAT was performed with moxifloxacin and ciprofloxacin using CD193 (CCR3) for basophil selection and CD203c or CD63 as activation markers. Stimulation with ciprofloxacin induced a significantly higher expression of CD63 in ciprofloxacin-allergic patients compared to moxifloxacin-allergic patients (P = 0.002). In patients allergic to moxifloxacin with anaphylactic shock, we have observed an increase in the percentage of cells that upregulate CD203c, whereas patients with anaphylaxis preferentially upregulate CD63. The best sensitivity-specificity was obtained using a cutoff of 3 and the culprit FQ, using CD203c for moxifloxacin-allergic patients (sensitivity = 36.4%; specificity = 94.4%), and CD63 for ciprofloxacin-allergic patients (sensitivity = 83.3%; specificity = 88.9%). A negative correlation was found between the upregulation of CD63 and CD203c and the time interval between the reaction occurrence and the performance of the test (Spearman r = -0.446; P 
dc.identifier.doi10.1097/MD.0000000000003679
dc.identifier.essn1536-5964
dc.identifier.pmcPMC4907647
dc.identifier.pmid27281069
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4907647/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1097/md.0000000000003679
dc.identifier.urihttp://hdl.handle.net/10668/10162
dc.issue.number23
dc.journal.titleMedicine
dc.journal.titleabbreviationMedicine (Baltimore)
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.organizationHospital Universitario Regional de Málaga
dc.page.numbere3679
dc.pubmedtypeJournal Article
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshBasophils
dc.subject.meshBiomarkers
dc.subject.meshFemale
dc.subject.meshFlow Cytometry
dc.subject.meshFluoroquinolones
dc.subject.meshFollow-Up Studies
dc.subject.meshHumans
dc.subject.meshHypersensitivity, Immediate
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshRetrospective Studies
dc.subject.meshTime Factors
dc.titleHypersensitivity to fluoroquinolones: The expression of basophil activation markers depends on the clinical entity and the culprit fluoroquinolone.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number95
dspace.entity.typePublication

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