<?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>2026-06-02T15:21:16Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/32582" metadataPrefix="qdc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/32582</identifier><datestamp>2026-02-03T10:59:56Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><qdc:qualifieddc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:qdc="http://dspace.org/qualifieddc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" 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>Study of binding and neutralising antibodies to interferon-β in two groups of relapsing-remitting multiple sclerosis patients.</dc:title>
   <dc:creator>Fernández Fernández, Óscar</dc:creator>
   <dc:creator>Mayorga Mayorga, Cristobalina</dc:creator>
   <dc:creator>Luque, Gloria</dc:creator>
   <dc:creator>Guerrero, Miguel</dc:creator>
   <dc:creator>Guerrero, Rocío</dc:creator>
   <dc:creator>Leyva-Fernández, Laura</dc:creator>
   <dc:creator>León-Martín, Antonio</dc:creator>
   <dc:creator>Blanca, Miguel</dc:creator>
   <dc:subject>Esclerosis múltiple - Tratamiento</dc:subject>
   <dcterms:abstract>Interferon (IFN)-β is generally considered an effective treatment for multiple sclerosis (MS); however, some patients do not respond to this therapy, possibly due to the production of neutralising antibodies (NAB) which can prevent the biological effect of IFN-β. We compared the two types of IFN-β, the glycosylated IFN-β1a and the non-glycosylated IFN-β1b, as their chemical differences may entail differing immunogenic capacities.&#xd;
We studied 22 relapsing-remitting MS patients treated with IFN-β1a and 31 treated with IFN-β1b for 1 year, using the same assay and criteria, to compare the two types of IFN-β in their ability to induce binding and neutralising antibodies and examined the correlation of the findings with the clinical data. Binding antibodies to IFN-β1a and IFN-β1b were determined by enzyme-linked immunosorbent assay. A bioassay was used to detect and quantify the NABs to IFN-β, measuring the capacity of NABs to block the antiviral resistance induced by IFNs. Binding antibodies were found in 32% of those treated with IFN-β1a and in 52% of those treated with IFN-β1b; NABs were found in 14% and 24%, respectively. Both groups showed a significant decrease in relapse rate during the first year of treatment. These results demonstrate that the IFN-β1b molecule is more immunogenic than the IFN-β1a molecule. This may be due to the non-glycosylated, chemical structure of the former, which can produce aggregates and enhance antibody production. No association was found between the presence of NABs and the clinical status of the patients.</dcterms:abstract>
   <dcterms:dateAccepted>2024-09-17T11:22:18Z</dcterms:dateAccepted>
   <dcterms:available>2024-09-17T11:22:18Z</dcterms:available>
   <dcterms:created>2024-09-17T11:22:18Z</dcterms:created>
   <dcterms:issued>2001</dcterms:issued>
   <dc:type>journal article</dc:type>
   <dc:identifier>Fernández O, Mayorga C, Luque G, Guerrero M, Guerrero R, Leyva L, León A, Blanca M. Study of binding and neutralising antibodies to interferon-beta in two groups of relapsing-remitting multiple sclerosis patients. J Neurol. 2001 May;248(5):383-8.</dc:identifier>
   <dc:identifier>https://hdl.handle.net/10630/32582</dc:identifier>
   <dc:identifier>10.1007/s004150170178</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:rights>open access</dc:rights>
   <dc:publisher>Springer Nature</dc:publisher>
</qdc:qualifieddc>
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