<?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>2026-04-17T05:45:31Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/7490" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/7490</identifier><datestamp>2024-06-06T14:03:15Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>com_2072_378071</setSpec><setSpec>col_2072_378092</setSpec><setSpec>col_2072_378097</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" 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://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Walo-Delgado, Paulette Esperanza</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Medina, Silvia</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Quintana, Ester</subfield>
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      <subfield code="a">Fernández-Velasco, José Ignacio</subfield>
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      <subfield code="a">Montalban Gairín, Xavier</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Midaglia Fernandez, Luciana</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Sainz de la Maza, Susana</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Comabella Lopez, Manuel</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Monreal, Enric</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2022-05-06T12:35:00Z</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2022-05-06T12:35:00Z</subfield>
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      <subfield code="c">2021-10</subfield>
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   <datafield ind2=" " ind1=" " tag="520">
      <subfield code="a">Células B; Alemtuzumab; Autoinmunidad</subfield>
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   <datafield ind2=" " ind1=" " tag="520">
      <subfield code="a">Limfòcits B; Alemtuzumab; Autoimmunitat</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="520">
      <subfield code="a">B cells; Alemtuzumab; Autoimmunity</subfield>
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      <subfield code="a">Objective: To explore if baseline blood lymphocyte profile could identify relapsing remitting multiple sclerosis (RRMS) patients at higher risk of developing secondary autoimmune adverse events (AIAEs) after alemtuzumab treatment.&#xd;
Methods: Multicenter prospective study including 57 RRMS patients treated with alemtuzumab followed for 3.25 [3.5-4.21] years, (median [interquartile range]). Blood samples were collected at baseline, and leukocyte subsets determined by flow cytometry. We had additional samples one year after the first cycle of alemtuzumab treatment in 39 cases.&#xd;
Results: Twenty-two patients (38.6%) developed AIAEs during follow-up. They had higher B-cell percentages at baseline (p=0.0014), being differences mainly due to plasmablasts/plasma cells (PB/PC, p=0.0011). Those with no AIAEs had higher percentages of CD4+ T cells (p=0.013), mainly due to terminally differentiated (TD) (p=0.034) and effector memory (EM) (p=0.031) phenotypes. AIAEs- patients also showed higher values of TNF-alpha-producing CD8+ T cells (p=0.029). The percentage of PB/PC was the best variable to differentiate both groups of patients. Baseline values >0.10% closely associated with higher AIAE risk (Odds ratio [OR]: 5.91, 95% CI: 1.83-19.10, p=0.004). When excluding the 12 patients with natalizumab, which decreases blood PB/PC percentages, being the last treatment before alemtuzumab, baseline PB/PC >0.1% even predicted more accurately the risk of AIAEs (OR: 11.67, 95% CI: 2.62-51.89, p=0.0007). The AIAEs+ group continued having high percentages of PB/PC after a year of alemtuzumab treatment (p=0.0058).&#xd;
Conclusions: A PB/PC percentage &lt;0.1% at baseline identifies MS patients at low risk of secondary autoimmunity during alemtuzumab treatment.​</subfield>
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      <subfield code="a">This work was supported by grants from Red Española de Esclerosis Múltiple (REEM) (RD16/0015/0001; RD16/0015/0004; RD16/0015/0006; RD16/0015/0013) and PI18/00572 integrated in the Plan Estatal I+D+I and co-funded by ISCIII-Subdirección General de Evaluación and Fondo Europeo de Desarrollo Regional (FEDER, “Una manera de hacer Europa”).</subfield>
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      <subfield code="a">Esclerosi múltiple - Tractament</subfield>
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      <subfield code="a">Cèl·lules B</subfield>
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      <subfield code="a">Autoimmunitat</subfield>
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      <subfield code="a">DISEASES::Nervous System Diseases::Autoimmune Diseases of the Nervous System::Demyelinating Autoimmune Diseases, CNS::Multiple Sclerosis::Multiple Sclerosis, Relapsing-Remitting</subfield>
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      <subfield code="a">Other subheadings::Other subheadings::Other subheadings::/drug therapy</subfield>
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      <subfield code="a">ANATOMY::Cells::Antibody-Producing Cells::B-Lymphocytes</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">ENFERMEDADES::enfermedades del sistema nervioso::enfermedades autoinmunitarias del sistema nervioso::enfermedades autoinmunes desmielinizantes del SNC::esclerosis múltiple::esclerosis múltiple recurrente-remitente</subfield>
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      <subfield code="a">Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">ANATOMÍA::células::células productoras de anticuerpos::linfocitos B</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Role of B Cell Profile for Predicting Secondary Autoimmunity in Patients Treated With Alemtuzumab</subfield>
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