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               <dc:title>Cytotoxic NK cells phenotype and activated lymphocytes are the main characteristics of patients with alcohol-associated liver disease</dc:title>
               <dc:creator>Zurera Egea, Coral</dc:creator>
               <dc:creator>Teniente Serra, Aina</dc:creator>
               <dc:creator>Fuster, Daniel</dc:creator>
               <dc:creator>Martínez Cáceres, Eva María</dc:creator>
               <dc:creator>Muga, Roberto</dc:creator>
               <dc:creator>Zuluaga Blanco, Yenny Paola</dc:creator>
               <dc:creator>Universitat Autònoma de Barcelona</dc:creator>
               <dc:subject>Cytotoxic NK cells</dc:subject>
               <dc:subject>Activated T cells</dc:subject>
               <dc:subject>NKT-like</dc:subject>
               <dc:subject>Alcohol-associated liver fbrosis</dc:subject>
               <dc:description>Altres ajuts: acords transformatius de la UAB</dc:description>
               <dc:description>T cells, natural killer (NK) and NKT cells have opposing actions in the development of alcohol-associated liver fibrosis. We aimed to evaluate the phenotype of NK cells, NKT cells and activated T cells in patients with alcohol use disorder (AUD) according to the presence of advanced liver fibrosis (ALF). Totally, 79 patients (51-years, 71% males) were admitted to treatment of AUD. ALF was defined as FIB4-score > 2.67. Immunophenotyping of NK cells (CD3CD56CD16, CD3CD56CD16, CD3CD56CD16), NKT-like (CD3CD56), and the activation status of CD4, CD8 and regulatory T cells (Tregs) were evaluated according to the HLA-DR expression. Patients had an AUD duration of 18 ± 11 years with a daily alcohol consumption of 155 ± 77 gr/day prior to hospital admission. The values of absolute cells were 2 ± 0.9 cells/L for total lymphocytes, 1054 ± 501 cells/µL for CD4, 540 ± 335 cells/µL for CD8, 49.3 ± 24.8 cells/µL for Tregs, 150.3 ± 97.5 cells/µL for NK cells and 69.8 ± 78.3 cells/µL for NKT-like. The percentage of total NK cells (11.3 ± 5.5% vs. 7 ± 4.3%, p &lt; 0.01), CD3CD56CD16 regarding total lymphocytes (9.7 ± 5.1% vs. 5.8 ± 3.9%, p &lt; 0.01), activated CD4 cells (5.2 ± 3.2% vs. 3.9 ± 3%, p = 0.04) and activated CD8 cells (15.7 ± 9.1% vs. 12.2 ± 9%, p = 0.05) were significantly higher in patients with ALF. The percentage of CD3CD56CD16 regarding NK cells (5.1 ± 3.4% vs. 7.6 ± 6.2%, p = 0.03) was significantly lower in patients with ALF. Activated Tregs (39.9 ± 11.5 vs. 32.4 ± 9.2, p = 0.06) showed a tendency to be higher in patients with ALF. The proportion of activated CD4 cells (r = 0.40, p &lt; 0.01) and activated CD8 cells (r = 0.51, p &lt; 0.01) was correlated with the proportion of NKT-like in patients without ALF. Patients with ALF presented an increased NK cytotoxic phenotype and activated T cells concomitant with a decreased NK cytokine-secreting phenotype.</dc:description>
               <dc:date>2023</dc:date>
               <dc:type>Article</dc:type>
               <dc:relation>Instituto de Salud Carlos III RD21/0009/0004</dc:relation>
               <dc:relation>Instituto de Salud Carlos III PI20/00883</dc:relation>
               <dc:relation>Clinical and Experimental Medicine ; Vol. 23, Num. 7 (november 2023), p. 3539-3547</dc:relation>
               <dc:rights>open access</dc:rights>
               <dc:rights>Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.</dc:rights>
               <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
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