<?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>2026-04-14T05:23:29Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:20.500.12327/3044" metadataPrefix="marc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:20.500.12327/3044</identifier><datestamp>2025-10-22T11:29:34Z</datestamp><setSpec>com_2072_4428</setSpec><setSpec>com_2072_4427</setSpec><setSpec>col_2072_487898</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">Almolda, Beatriz</subfield>
      <subfield code="e">author</subfield>
   </datafield>
   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Costa, Manuela</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Montoya, Maria</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">González, Berta</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Castellano, Bernardo</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2011-11-07</subfield>
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      <subfield code="a">Experimental autoimmune encephalomyelitis (EAE), a well-established model of multiple sclerosis, is characterised by&#xd;
microglial activation and lymphocyte infiltration. Induction of EAE in Lewis rats produces an acute monophasic disease&#xd;
characterised by a single peak of disability followed by a spontaneous and complete recovery and a subsequent tolerance&#xd;
to further immunizations. In the current study we have performed a detailed analysis of the dynamics of different&#xd;
lymphocyte populations and cytokine profile along the induction, peak, recovery and post-recovery phases in this&#xd;
paradigm. MBP-injected rats were sacrificed attending exclusively to their clinical score, and the different populations of Tlymphocytes as well as the dynamics of different pro- and anti-inflammatory cytokines were analysed in the spinal cord by&#xd;
flow cytometry, immunohistochemistry and ELISA. Our results revealed that, during the induction and peak phases, in&#xd;
parallel to an increase in symptomatology, the number of CD3+ and CD4+ cells increased progressively, showing a Th1&#xd;
phenotype, but unexpectedly during recovery, although clinical signs progressively decreased, the number and proportion&#xd;
of CD3+ and CD4+ populations remained unaltered. Interestingly, during this recovery phase, we observed a marked&#xd;
decrease of Th1 and an important increase in Th17 and T-reg cells. Moreover, our results indicate a specific cytokine&#xd;
expression profile along the EAE course characterized by no changes of IL10 and IL17 levels, decrease of IL21 on the peak,&#xd;
and high IL22 levels during the induction and peak phases that markedly decrease during recovery. In summary, these&#xd;
results revealed the existence of a specific pattern of lymphocyte infiltration and cytokine secretion along the different&#xd;
phases of the acute EAE model in Lewis rat that differs from those already described in chronic or relapsing-remitting mouse&#xd;
models, where Th17-cells were found mostly during the peak, suggesting a specific role of these lymphocytes and cytokines&#xd;
in the evolution of this acute EAE model.</subfield>
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      <subfield code="a">Almolda, Beatriz, Manuela Costa, Maria Montoya, Berta González, and Bernardo Castellano. 2011. “Increase in Th17 and T-reg Lymphocytes and Decrease of IL22 Correlate With the Recovery Phase of Acute EAE IN Rat.” PloS One 6 (11): e27473. doi: 10.1371/journal.pone.0027473</subfield>
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      <subfield code="a">1932-6203</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12327/3044</subfield>
   </datafield>
   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">https://doi.org/10.1371/journal.pone.0027473</subfield>
   </datafield>
   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Increase in Th17 and T-reg Lymphocytes and Decrease of IL22 Correlate with the Recovery Phase of Acute EAE IN Rat</subfield>
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