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               <dc:title>Increase in Th17 and T-reg Lymphocytes and Decrease of IL22 Correlate with the Recovery Phase of Acute EAE IN Rat</dc:title>
               <dc:creator>Almolda, Beatriz</dc:creator>
               <dc:creator>Costa, Manuela</dc:creator>
               <dc:creator>Montoya, Maria</dc:creator>
               <dc:creator>González, Berta</dc:creator>
               <dc:creator>Castellano, Bernardo</dc:creator>
               <dc:contributor>Producció Animal</dc:contributor>
               <dc:contributor>Sanitat Animal</dc:contributor>
               <dc:description>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.</dc:description>
               <dc:date>2025-10-22T11:29:34Z</dc:date>
               <dc:date>2025-10-22T11:29:34Z</dc:date>
               <dc:date>2011-11-07</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:identifier>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</dc:identifier>
               <dc:identifier>1932-6203</dc:identifier>
               <dc:identifier>http://hdl.handle.net/20.500.12327/3044</dc:identifier>
               <dc:identifier>https://doi.org/10.1371/journal.pone.0027473</dc:identifier>
               <dc:language>eng</dc:language>
               <dc:relation>PLoS ONE</dc:relation>
               <dc:relation>MICINN/Programa Nacional de Proyectos de Investigación Fundamental/BFU2008-04407/ES/Caracterización de subpoblaciones de células de microglia/macrófagos del CNS que pueden modular la función linfocitaria en microambientes inflamatorios y antiinflamatorios/BFI</dc:relation>
               <dc:relation>MICINN/Programa Nacional de Proyectos de Investigación Fundamental/BFU2011-27400/ES/Implicación de los astrocitos y la microglia en la terminación de la respuesta inmunitaria y el establecimeinto de la tolerancia en diferentes paradigmas/</dc:relation>
               <dc:rights>http://creativecommons.org/licenses/by/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:rights>Attribution 4.0 International</dc:rights>
               <dc:publisher>Public Library of Science</dc:publisher>
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