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dc.contributor.authorGarcia-Broncano, Pilar
dc.contributor.authorMedrano, Luz Maria
dc.contributor.authorBerenguer, Juan
dc.contributor.authorGonzález-García, Juan
dc.contributor.authorJiménez-Sousa, Maria Ángeles
dc.contributor.authorCarrero, Ana
dc.contributor.authorHontañón, Víctor
dc.contributor.authorGuardiola Tey, Josep Maria
dc.contributor.authorCrespo, Manuel
dc.contributor.authorQuereda, Carmen
dc.contributor.authorSanz, José
dc.contributor.authorGarcía-Gómez, Ana Belen
dc.contributor.authorJimenez, Jose Luis
dc.contributor.authorResino, Salvador
dc.contributor.authorGESIDA 3603b Study Group
dc.date.accessioned2021-06-17T16:45:08Z
dc.date.available2021-06-17T16:45:08Z
dc.date.issued2018
dc.identifier.citationGarcia-Broncano, Pilar; Medrano, Luz Maria; Berenguer, Juan [et al.]. Dysregulation of the immune system in HIV/HCV-coinfected patients according to liver stiffness status. Cells, 7(11), 196. Disponible en: <https://www.mdpi.com/2073-4409/7/11/196>. Fecha de acceso: 17 jun, 2021. DOI: 10.3390/cells7110196ca
dc.identifier.issn2073-4409ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/2636
dc.description.abstractBackground: Advanced cirrhosis is related to alterations in immunity. We aimed to evaluate the levels of peripheral CD4+ T cells (Tregs) and plasma cytokine in patients coinfected with human immunodeficiency virus and hepatitis C virus (HIV/HCV) according to liver fibrosis stages [evaluated as liver stiffness measure (LSM)] and their linear relationship. Methods: We performed a cross-sectional study on 238 HIV/HCV-coinfected patients (119 had <12.5 kPa, 73 had 12.5–25 kPa, and 46 had >25 kPa). Peripheral T-cell subsets were phenotyped by flow cytometry, plasma biomarkers were assessed by multiplex immunoassays, and LSM was assessed by transient elastography. Results: We found HIV/HCV-coinfected patients had higher values of CD4+ Tregs (p < 0.001), memory Tregs (p ≤ 0.001), and plasma cytokine levels [IFN-γ (p ≤ 0.05) and IL-10 (p ≤ 0.01)] compared with healthy donors and HIV-monoinfected patients. In the multivariate analysis, higher LSM values were associated with reduced levels of IL-10 (adjusted arithmetic mean ratio (aAMR) = 0.83; p = 0.019), IL-2 (aAMR = 0.78; p = 0.017), TNF-α (aAMR = 0.67; p < 0.001), and IL-17A (aAMR = 0.75; p = 0.006). When we focus on HIV/HCV-coinfected patients analyzed by LSM strata, patients with ≥25 kPa had lower values of IL-2 (aAMR = 0.66; p = 0.021), TNF-α (aAMR = 0.565; p = 0.003), and IL-17A (aAMR = 0.58; p = 0.003) than patients with <12.5 kPa. Conclusion: HIV/HCV-coinfected patients showed an immunosuppressive profile compared to healthy controls and HIV-monoinfected patients. Additionally, HIV/HCV-coinfected patients with advanced cirrhosis (LSM ≥ 25 kPa) had the lowest plasma values of cytokines related to Th1 (IL-2 and TNF-α) and Th17 (IL-17A) response.en
dc.format.extent16ca
dc.language.isoengca
dc.publisherMDPIca
dc.relation.ispartofCellsca
dc.relation.ispartofseries7;11
dc.rights© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open accessarticle distributed under the terms and conditions of the Creative Commons Attribution(CC BY) license (http://creativecommons.org/licenses/by/4.0/).en
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.otherHepatitis C crònicaca
dc.subject.otherVIHca
dc.subject.otherCirrosica
dc.subject.otherCèl·lules Tregca
dc.subject.otherCitocinesca
dc.subject.otherDisfunció immuneca
dc.subject.otherHepatitis C crónicaes
dc.subject.otherVIHes
dc.subject.otherCirrosises
dc.subject.otherCélulas Treges
dc.subject.otherCitocinases
dc.subject.otherDisfunción inmunees
dc.subject.otherChronic hepatitis C.en
dc.subject.otherHIVen
dc.subject.otherCirrhosisen
dc.subject.otherTreg cellsen
dc.subject.otherCytokinesen
dc.subject.otherImmune dysfunctionen
dc.titleDysregulation of the immune system in HIV/HCV-coinfected patients according to liver stiffness statusen
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.subject.udc61ca
dc.subject.udc616.9ca
dc.identifier.doihttps://dx.doi.org/10.3390/cells7110196ca


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© 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open accessarticle distributed under the terms and conditions of the Creative Commons Attribution(CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0/
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