<?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>2026-04-13T01:39:34Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2072/485383" metadataPrefix="mets">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2072/485383</identifier><datestamp>2025-10-27T13:36:30Z</datestamp><setSpec>com_2072_98</setSpec><setSpec>col_2072_378192</setSpec></header><metadata><mets xmlns="http://www.loc.gov/METS/" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" ID="&#xa;&#x9;&#x9;&#x9;&#x9;DSpace_ITEM_2072-485383" TYPE="DSpace ITEM" PROFILE="DSpace METS SIP Profile 1.0" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd" OBJID="&#xa;&#x9;&#x9;&#x9;&#x9;hdl:2072/485383">
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                  <mods:namePart>Pesqué, David</mods:namePart>
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                  <mods:namePart>Andrades, Evelyn</mods:namePart>
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                  <mods:namePart>Berenguer-Molins, Pau</mods:namePart>
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                  <mods:namePart>Perera-Bel, Júlia</mods:namePart>
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                  <mods:namePart>Clarós, Miquel</mods:namePart>
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                  <mods:namePart>Bódalo-Torruella, Marta</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Gonzàlez-Farré, Mònica</mods:namePart>
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               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Gallardo, Fernando</mods:namePart>
               </mods:name>
               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Pujol Vallverdú, Ramón M.</mods:namePart>
               </mods:name>
               <mods:name>
                  <mods:role>
                     <mods:roleTerm type="text">author</mods:roleTerm>
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                  <mods:namePart>Giménez-Arnau, Ana M</mods:namePart>
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                  <mods:dateIssued encoding="iso8601">2025</mods:dateIssued>
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               <mods:abstract>Altres ajuts: acords transformatius de la UABAltres ajuts: LEO Foundation (LF-OC-23-001209)Background: Immune mechanisms underlying elicitation in allergic contact dermatitis (ACD) have yet to be fully elucidated. Previous studies have shown a double-faceted nature of ACD with both common biomarkers among different allergens and allergen73 specific imprinting, albeit with discordance in terms of relevant pathways involved. Several factors, including co-existing atopic dermatitis, may influence immune reactions. We aim to characterize molecular signatures and their immune mechanisms of different relevant allergens (nickel, 2-hydroxyethylmethacrylate [2-HEMA], methylisothiazolinone [MIT], formaldehyde) in strong and extreme positive (2/3+) patch test reactions of patients without atopic dermatitis. Methods: A transcriptomic analysis of 40 skin biopsies of ACD reactions (11 nickel, 10 MIT, 10 2-HEMA, 9 formaldehyde) and 19 controls (petrolatum-occluded skin) was performed using RNA sequencing. Differentially-expressed genes (DEG) were assessed and enriched functional pathways were obtained with an over-representation analysis for allergens. Results: ACD molecular profiling revealed a strong, common imprinting of DEG among allergens versus controls (n=814), with further partially-shared DEG among allergens (n=664) and allergen-specific DEG (n=430). The most relevant shared pathways were associated with immune adaptive and innate responses. All allergens exhibited mixed effector immune responses, mainly type 1 and 3 immunity, and, to a lesser extent, type 2 immunity. Furthermore, partially-shared and unique DEG were associated with further inflammatory pathways, particularly for nickel and 2-HEMA. Conclusions: This study confirms shared ACD imprinting among different allergens and shared pathways' predominant role in ACD elicitation in patients without atopic dermatitis, alongside allergen-specific immune processes and mixed effector responses (type 1, 3 and 2).</mods:abstract>
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               <mods:accessCondition type="useAndReproduction">open access Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, sempre que no sigui amb finalitats comercials, i sempre que es reconegui l'autoria de l'obra original. https://creativecommons.org/licenses/by-nc/4.0/</mods:accessCondition>
               <mods:subject>
                  <mods:topic>Contact dermatitis</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Allergic</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Transcriptomic</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Immune</mods:topic>
               </mods:subject>
               <mods:subject>
                  <mods:topic>Patch test</mods:topic>
               </mods:subject>
               <mods:titleInfo>
                  <mods:title>Transcriptomic analysis of allergic patch test reactions in non-atopic patients: a comparative study across multiple allergens</mods:title>
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               <mods:genre>Article</mods:genre>
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