<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-30T17:26:40Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/45417" metadataPrefix="mods">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/45417</identifier><datestamp>2026-04-10T09:19:47Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><mods:mods xmlns:doc="http://www.lyncode.com/xoai" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Tesfaye Ayane, Amene</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Salas, María</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Benede, Sara</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Rodríguez-Sánchez, Maria J.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Rodríguez-Sojo, María J.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Jiménez-Sánchez, Isabel M.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Bogas, Gador</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Pérez-de-Inestrosa-Villatoro, Ezequiel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Mayorga, Cristobalina</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Paris, Juan L.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Rodríguez-Nogales, Alba</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Torres-Jaén, María Josefa</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Montañez-Vega, María Isabel</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2026-02-12T12:23:12Z</mods:dateAvailable>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2026</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">A. T. Ayane, M. Salas, S. Benede, et al., “ Dendrimeric Antigens for Passive Mast Cell Activation in the Evaluation of Amoxicillin Allergy,” Allergy (2026): 1–12, https://doi.org/10.1111/all.70250.</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/10630/45417</mods:identifier>
   <mods:identifier type="doi">https://doi.org/10.1111/all.70250</mods:identifier>
   <mods:abstract>Background: Amoxicillin (AX) is frequently implicated in immediate IgE-mediated allergic reactions. Diagnosis is challenging,highlighting the need for new approaches enhancing in vitro sensitivity and specificity. Engineered nanostructures can mimicimmunological recognition of hapten-carrier conjugates, offering a strategy to improve diagnostic accuracy.Methods: Dendrimeric Antigens (DeAns), with controlled size (1st–5th generation) and multivalent AX determinants (8–128 units, respectively), were synthesized for in vitro immunological evaluation. In vitro IgE recognition was studied by com-petitive radio-immunoassay. Allergenic activity was evaluated in mouse bone marrow-derived mast cells (MC) sensitized withmouse anti-AX IgE monoclonal antibody and humanized RBL-2H3 (huRBL-2H3) and LUVA cells sensitized with sera fromβ-lactam-allergic subjects and tolerant controls, measuring degranulation in response to DeAns stimulation.Results: Five different DeAns were obtained as pure compounds. All DeAns were recognized by AX-sIgE. A clear size-dependent activation pattern was observed in the three cell models: lower-generation (1st–2nd) DeAns failed to induce degranu-lation, whereas DeAns of bigger size (3rd–5th generation) triggered significant, dose-dependent activation. Notably, no activationwas observed in tolerants and unsensitized cells or with blank dendrimers. In patient-sera assays, the passive MC activation test(pMAT) with DeAns provided complete diagnostic discrimination, with activation restricted to AX-allergic patients.Conclusions: DeAns are effective platforms for investigating effector cell activation in AX allergy. By fine-tuning structuralattributes—size and multivalence—we reveal the promising utility of DeAns in pMAT that leverage commercial cell lines andpatient sera. This approach could address key limitations of β-lactam allergy diagnostics, enabling more reliable and standard-ized in vitro testing.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">http://creativecommons.org/licenses/by-nc-nd/4.0/</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 International</mods:accessCondition>
   <mods:subject>
      <mods:topic>Antibióticos</mods:topic>
   </mods:subject>
   <mods:subject>
      <mods:topic>Alergia a los medicamentos</mods:topic>
   </mods:subject>
   <mods:subject>
      <mods:topic>Antibióticos betalactámicos</mods:topic>
   </mods:subject>
   <mods:subject>
      <mods:topic>Amoxicilina</mods:topic>
   </mods:subject>
   <mods:titleInfo>
      <mods:title>Dendrimeric antigens for passive mast cell activation in the evaluation of amoxicillin allergy</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods>
</metadata></record></GetRecord></OAI-PMH>