<?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>2026-04-13T18:26:37Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2117/21281" metadataPrefix="qdc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2117/21281</identifier><datestamp>2026-02-07T11:54:29Z</datestamp><setSpec>com_2072_1033</setSpec><setSpec>col_2072_452950</setSpec></header><metadata><qdc:qualifieddc xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://purl.org/dc/elements/1.1/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dc.xsd http://purl.org/dc/terms/ http://dublincore.org/schemas/xmls/qdc/2006/01/06/dcterms.xsd http://dspace.org/qualifieddc/ http://www.ukoln.ac.uk/metadata/dcmi/xmlschema/qualifieddc.xsd">
   <dc:title>Amygdalin analogues inhibit INF-gamma signalling reducing inflammatory response in human keratinocytes (HaCat)</dc:title>
   <dc:creator>Paoletti, Iole</dc:creator>
   <dc:creator>De Gregorio, Vicenza</dc:creator>
   <dc:creator>Baroni, Adone</dc:creator>
   <dc:creator>Tufano, Maria Antonieta</dc:creator>
   <dc:creator>Donnarumma, Giovanna</dc:creator>
   <dc:creator>Pérez González, Juan Jesús</dc:creator>
   <dc:subject>Àrees temàtiques de la UPC::Enginyeria química</dc:subject>
   <dc:subject>Peptides</dc:subject>
   <dc:subject>Psoriasis</dc:subject>
   <dc:subject>peptide T</dc:subject>
   <dc:subject>amygdalin analogues</dc:subject>
   <dc:subject>NHEK cells</dc:subject>
   <dc:subject>psoriasis</dc:subject>
   <dc:subject>Pèptids</dc:subject>
   <dc:subject>Psoriasi</dc:subject>
   <dcterms:abstract>Peptide T (PT), an octapeptide fragment located in the V2 region of the HIV-1 gp120-&#xd;
coating protein, appears to be bene&#xd;
fi&#xd;
cial in the treatment of psoriasis. Our previous investigations&#xd;
suggest that keratinocytes play a key role in conditioning the therapeutic effects of PT in psoriasis.&#xd;
The aim of this study was to explore the effects of PT and the peptidomimetic natural products,&#xd;
Dhurrin and Prunasin, on the expression of the IL-6, IL-8, IL-23, HSP70 and ICAM-1 on IFN-&#xd;
γ&#xd;
and TNF-&#xd;
α&#xd;
-NHEK activated cells. Moreover, we analysed the interference of PT and its analogues&#xd;
through STAT-3 activation. Our results show that the analogues tested exhibit the bene&#xd;
fi&#xd;
cial biol-&#xd;
ogical effects of PT, suggesting the primary role of keratinocytes upon which PT and the peptido-&#xd;
mimetics act directly, by reducing proin&#xd;
fl&#xd;
ammatory responses. Its reduction appears to be important&#xd;
for therapeutic approach in psoriasis pathogenesis</dcterms:abstract>
   <dcterms:abstract>Peer Reviewed</dcterms:abstract>
   <dcterms:abstract>Postprint (published version)</dcterms:abstract>
   <dcterms:issued>2013-12-02</dcterms:issued>
   <dc:type>Article</dc:type>
   <dc:relation>http://link.springer.com/article/10.1007%2Fs10753-013-9670-7</dc:relation>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/3.0/es/</dc:rights>
   <dc:rights>Restricted access - publisher's policy</dc:rights>
   <dc:rights>Attribution-NonCommercial-NoDerivs 3.0 Spain</dc:rights>
</qdc:qualifieddc></metadata></record></GetRecord></OAI-PMH>