<?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>2026-06-27T10:18:12Z</responseDate><request verb="GetRecord" identifier="oai:docta.ucm.es:20.500.14352/94459" metadataPrefix="mods">https://docta.ucm.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:docta.ucm.es:20.500.14352/94459</identifier><datestamp>2025-03-18T15:11:15Z</datestamp><setSpec>com_20.500.14352_14</setSpec><setSpec>col_20.500.14352_15</setSpec></header><metadata><mods:mods xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>Lamana Domínguez, Amalia</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Ortiz, Ana</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Alvaro-Gracia, José</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Díaz-Sánchez, Belén </mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Novalbos, Jesús</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>García-Vicuña, Rosario</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>González-Alvaro, Isodoro</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2024-01-22T15:30:56Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2024-01-22T15:30:56Z</mods:dateAccessioned>
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   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2010</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Amalia Lamana, Ana M Ortiz, José M Alvaro-Gracia, Belén Díaz-Sánchez, Jesús Novalbos, Rosario García-Vicuña, Isidoro González-Álvaro . Characterization of serum interleukin-15 in healthy volunteers and patients with early arthritis to assess its potential use as a biomarker. European Cytokine Network. 2010;21(3):186-194. doi:10.1684/ecn.2010.0203</mods:identifier>
   <mods:identifier type="issn">1148-5493</mods:identifier>
   <mods:identifier type="doi">10.1684/ecn.2010.0203</mods:identifier>
   <mods:identifier type="uri">https://hdl.handle.net/20.500.14352/94459</mods:identifier>
   <mods:identifier type="essn">1952-4005</mods:identifier>
   <mods:identifier type="officialurl">https://www.jle.com/10.1684/ecn.2010.0203</mods:identifier>
   <mods:abstract>As interleukin-15 (IL-15) has been implicated in the pathophysiology of rheumatoid arthritis, we analysed the serum IL-15 (sIL-15) levels in healthy subjects and patients with early arthritis to establish a cut-off point that might serve to define elevated sIL-15. This is an initial step to determine whether sIL-15 has the potential for use as a biomarker for patients with early arthritis. The IL-15 concentration was measured in serum obtained from 161 healthy controls and from 174 patients with early arthritis, and the relationship between the expression of the two IL-15 mRNA variants and the sIL-15 levels was also assessed. In healthy controls, the median sIL-15 value was 0.83 [interquartile range (IQR) 0-8.68] pg/mL; there was no significant difference in the sIL-15 values according to gender [median level in males was 1.99 (IQR: 0-8.68) pg/mL and in females 0.50 (0-8.25) pg/mL: p = 0.821]. Moreover, sIL-15 levels did not correlate with age (r = 0.033, p = 0.685), and they did not display a clear circadian rhythm in healthy donors, with the median values for IL-15 close to zero at each time tested. In the light of these findings, we considered that sIL-15 was elevated if its concentration was above 20 pg/mL, since this cut-off point corresponded to the 90th percentile for this healthy population. We found that 30% of the patients with early arthritis had sIL-15 values > 20 pg/mL. The levels of sIL-15 did not correlate with disease duration in early arthritis patients, nor did they fluctuate with changes in disease activity over the follow-up period. In addition, the high level of sIL15 in patients was not associated with alterations in the alternative splicing of the IL-15 mRNA, favouring the variant that produces the protein with a long signal peptide for secretion. Serum IL-15 levels were increased in a subpopulation of patients with early arthritis, indicating that this measure may serve as a biomarker for this condition. Further studies will be necessary to determine whether the clinical evolution or response to treatment of patients with high sIL-15 levels differs.</mods:abstract>
   <mods:language>
      <mods:languageTerm>eng</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">restricted access</mods:accessCondition>
   <mods:titleInfo>
      <mods:title>Characterization of serum interleukin-15 in healthy volunteers and patients with early arthritis to assess its potential use as a biomarker</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
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