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                  <mods:namePart>García-Gasalla, Mercedes</mods:namePart>
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                  <mods:namePart>Berman-Riu, Maria</mods:namePart>
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                  <mods:namePart>Rodríguez, Adrián</mods:namePart>
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                  <mods:namePart>Iglesias, Amanda</mods:namePart>
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                  <mods:namePart>Fraile-Ribot, Pablo</mods:namePart>
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                  <mods:namePart>Toledo Pons, Nuria</mods:namePart>
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                  <mods:namePart>Pol-Pol, Elisabet</mods:namePart>
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                  <mods:namePart>Ferré Beltrán, Adrián</mods:namePart>
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                  <mods:namePart>Artigues Serra, Francisca</mods:namePart>
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                  <mods:namePart>Martin Pena, Maria Luisa</mods:namePart>
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                  <mods:namePart>Pons De Ves, Jaime</mods:namePart>
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                  <mods:namePart>Murillas Angoiti, Javier</mods:namePart>
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                  <mods:namePart>Oliver, Antonio</mods:namePart>
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                  <mods:namePart>Riera, Melchor</mods:namePart>
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                  <mods:namePart>Ferrer Balaguer, Juana Maria</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-10-09T06:34:11Z</mods:dateAccessioned>
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                  <mods:dateAvailable encoding="iso8601">2024-10-09T06:34:11Z</mods:dateAvailable>
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                  <mods:dateIssued encoding="iso8601">2023-09</mods:dateIssued>
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               <mods:identifier type="citation">Garcia-Gasalla M, Berman-Riu M, Rodriguez A, Iglesias A, Fraile-Ribot PA, Toledo-Pons N, et al. Elevated complement C3 and increased CD8 and type 1 helper lymphocyte T populations in patients with post-COVID-19 condition. Cytokine. 2023 Sep;169:156295.</mods:identifier>
               <mods:identifier type="other">https://hdl.handle.net/20.500.13003/19378</mods:identifier>
               <mods:identifier type="uri">https://hdl.handle.net/20.500.12105/23654</mods:identifier>
               <mods:identifier type="pubmedID">37453328</mods:identifier>
               <mods:identifier type="doi">10.1016/j.cyto.2023.156295</mods:identifier>
               <mods:identifier type="e-issn">1096-0023</mods:identifier>
               <mods:identifier type="journal">Cytokine</mods:identifier>
               <mods:identifier type="scopus">2-s2.0-85165026253</mods:identifier>
               <mods:identifier type="wos">1043760700001</mods:identifier>
               <mods:identifier type="pui">L2025720741</mods:identifier>
               <mods:abstract>Background: Biological markers associated to post-COVID-19 condition (PCC) have not been clearly identified. Methods: Eighty-two patients attending our post-COVID-19 outpatient clinic were recruited and classified as fully recovered (40.2%) or presenting with PCC (59.8%). Clinical and radiological data, laboratory markers, cytokines, and lymphocyte populations were analyzed. Results: Median number of days after hospitalization was 78.5 [p25-p75: 60-93] days. PCC was significantly more frequent in women, in patients with a previously critical COVID-19, and in those with two or more comorbidities. No differences were found in lymphocyte counts, ferritin, C-reactive protein, D-dimer or sCD25, IL-1β, IL-1Ra, IL-6, CXCL8, IL-17A, IL-18, IL-22, IFN-γ, TNF-α, and IL-10 cytokines levels. PCC patients showed significantly higher levels of complement factor C3 than fully recovered patients: median C3 128 mg/dL [p25-p75:107-135] vs 111 mg/dL [p25-p75: 100-125] (p =.005), respectively. In the flow cytometry assessment of peripheral blood lymphocyte subpopulations, PCC patients showed significantly increased CD8 populations compared to fully recovered patients: median CD8: 529 [p25-p75: 384-683] vs 370/mm3 [p25-p75:280-523], p =.007. When type 1, 2, 17/22, and 17.1 helper and follicular T lymphocyte subpopulations were analyzed, the frequency of Th1 was significantly higher in PCC patients compared to fully recovered patients (30% vs 38.5%, p =.028). Conclusion: Patients with a post-COVID-19 condition showed significantly increased immunological parameters of inflammation (complement factor C3 and CD8 and Th1 T lymphocyte populations) compared to fully recovered patients. These parameters could be used as biological markers of this condition.</mods:abstract>
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                  <mods:title>Elevated complement C3 and increased CD8 and type 1 helper lymphocyte T populations in patients with post-COVID-19 condition</mods:title>
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               <mods:genre>research article</mods:genre>
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