Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease

Autores
Bertot, Gustavo
Año de publicación
2021
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fil: Bertot, Gustavo. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina.
Fil: The immune response is critical in NAFLD pathogenesis, but the liver infiltrate’s composition and the role of each T cell population is still up for debate. To characterize liver pathogenesis in pediatric and adult cases, frequency and localization of immune cell populations [Cytotoxic T Lymphocytes (CD8+), T helper Lymphocytes (CD4+), Regulatory T lymphocytes (Foxp3+) and Th17 (IL-17A+)] were evaluated. In portal/periportal (P/P) tracts, both age groups displayed a similar proportion of CD8+ and CD4+ lymphocytes. However, comparable Foxp3+ and IL-17A+ cell frequencies were observed in pediatric cases, meanwhile, in adults Foxp3+ was higher than IL-17A+ cells. Interestingly, IL-17A+ lymphocytes seemed to be nearly exclusive of P/P area in both age groups. In intralobular areas, both pediatric and adult cases showed CD8+ lymphocytes predominance with lower frequencies of CD4+ lymphocytes followed by Foxp3+ . Severe inflammation was associated with higher intralobular Foxp3+ lymphocytes (p = 0.026) in children, and lower P/P Foxp3+ and higher IL-17A+ lymphocytes in adults. All cases with fibrosis ≥ 2 displayed P/P low Foxp3+ and high IL-17A+ lymphocyte counts. Pediatric cases with worse steatosis showed high P/P CD4+ (p = 0.023) and intralobular CD8+ (p = 0.027) and CD4+ cells (p = 0.012). In NAFLD cases, the lymphocyte liver infiltrate composition differs between histological areas. Treg and Th17 balance seems to condition damage progression, denoting their important role in pathogenesis.
Materia
ARTICULO
MEDICINA
LINFOCITOS HEPATICOS
HIGADO GRASO
Nivel de accesibilidad
acceso abierto
Condiciones de uso
Repositorio
Repositorio Institucional (Fundacion Barceló)
Institución
Fundación H. A. Barceló
OAI Identificador
oai:repositorio.barcelo.edu.ar:123456789/251

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network_name_str Repositorio Institucional (Fundacion Barceló)
spelling Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver diseaseBertot, GustavoARTICULOMEDICINALINFOCITOS HEPATICOSHIGADO GRASOFil: Bertot, Gustavo. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina.Fil: The immune response is critical in NAFLD pathogenesis, but the liver infiltrate’s composition and the role of each T cell population is still up for debate. To characterize liver pathogenesis in pediatric and adult cases, frequency and localization of immune cell populations [Cytotoxic T Lymphocytes (CD8+), T helper Lymphocytes (CD4+), Regulatory T lymphocytes (Foxp3+) and Th17 (IL-17A+)] were evaluated. In portal/periportal (P/P) tracts, both age groups displayed a similar proportion of CD8+ and CD4+ lymphocytes. However, comparable Foxp3+ and IL-17A+ cell frequencies were observed in pediatric cases, meanwhile, in adults Foxp3+ was higher than IL-17A+ cells. Interestingly, IL-17A+ lymphocytes seemed to be nearly exclusive of P/P area in both age groups. In intralobular areas, both pediatric and adult cases showed CD8+ lymphocytes predominance with lower frequencies of CD4+ lymphocytes followed by Foxp3+ . Severe inflammation was associated with higher intralobular Foxp3+ lymphocytes (p = 0.026) in children, and lower P/P Foxp3+ and higher IL-17A+ lymphocytes in adults. All cases with fibrosis ≥ 2 displayed P/P low Foxp3+ and high IL-17A+ lymphocyte counts. Pediatric cases with worse steatosis showed high P/P CD4+ (p = 0.023) and intralobular CD8+ (p = 0.027) and CD4+ cells (p = 0.012). In NAFLD cases, the lymphocyte liver infiltrate composition differs between histological areas. Treg and Th17 balance seems to condition damage progression, denoting their important role in pathogenesis.Nature Portfolio Scientific Reports (2021) 11:5129Cairoli, VictoriaDe Matteo, ElenaRios, DanielaLezama, CarolGaloppo, MarcelaCasciato, PaolaMullen, EduardoGiadans, CeciliaPreciado, Maria VictoriaValva, Pamela2021-07-022025-07-11T23:46:23Zinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttps://repositorio.barcelo.edu.ar/greenstone/collect/investig/index/assoc/HASH37b2.dir/BRC_122_MED_BA.pdfhttp://repositorio.barcelo.edu.ar/greenstone/collect/investig/index/assoc/HASH37b2.dir/BRC_122_MED_BA.pdfenginfo:eu-repo/semantics/openAccessreponame:Repositorio Institucional (Fundacion Barceló)instname:Fundación H. A. Barceló2025-10-23T11:16:34Zoai:repositorio.barcelo.edu.ar:123456789/251instacron:BARCELOInstitucionalhttp://repositorio.barcelo.edu.ar/greenstone/cgi-bin/library.cgiUniversidad privadaNo correspondehttp://repositorio.barcelo.edu.ar/greenstone/cgi-bin/oaiserver.cgilrodriguezares@barcelo.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:a2025-10-23 11:16:34.954Repositorio Institucional (Fundacion Barceló) - Fundación H. A. Barcelófalse
dc.title.none.fl_str_mv Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
title Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
spellingShingle Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
Bertot, Gustavo
ARTICULO
MEDICINA
LINFOCITOS HEPATICOS
HIGADO GRASO
title_short Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
title_full Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
title_fullStr Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
title_full_unstemmed Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
title_sort Hepatic lymphocytes involved in the pathogenesis of pediatric and adult non‑alcoholic fatty liver disease
dc.creator.none.fl_str_mv Bertot, Gustavo
author Bertot, Gustavo
author_facet Bertot, Gustavo
author_role author
dc.contributor.none.fl_str_mv Cairoli, Victoria
De Matteo, Elena
Rios, Daniela
Lezama, Carol
Galoppo, Marcela
Casciato, Paola
Mullen, Eduardo
Giadans, Cecilia
Preciado, Maria Victoria
Valva, Pamela
dc.subject.none.fl_str_mv ARTICULO
MEDICINA
LINFOCITOS HEPATICOS
HIGADO GRASO
topic ARTICULO
MEDICINA
LINFOCITOS HEPATICOS
HIGADO GRASO
dc.description.none.fl_txt_mv Fil: Bertot, Gustavo. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina.
Fil: The immune response is critical in NAFLD pathogenesis, but the liver infiltrate’s composition and the role of each T cell population is still up for debate. To characterize liver pathogenesis in pediatric and adult cases, frequency and localization of immune cell populations [Cytotoxic T Lymphocytes (CD8+), T helper Lymphocytes (CD4+), Regulatory T lymphocytes (Foxp3+) and Th17 (IL-17A+)] were evaluated. In portal/periportal (P/P) tracts, both age groups displayed a similar proportion of CD8+ and CD4+ lymphocytes. However, comparable Foxp3+ and IL-17A+ cell frequencies were observed in pediatric cases, meanwhile, in adults Foxp3+ was higher than IL-17A+ cells. Interestingly, IL-17A+ lymphocytes seemed to be nearly exclusive of P/P area in both age groups. In intralobular areas, both pediatric and adult cases showed CD8+ lymphocytes predominance with lower frequencies of CD4+ lymphocytes followed by Foxp3+ . Severe inflammation was associated with higher intralobular Foxp3+ lymphocytes (p = 0.026) in children, and lower P/P Foxp3+ and higher IL-17A+ lymphocytes in adults. All cases with fibrosis ≥ 2 displayed P/P low Foxp3+ and high IL-17A+ lymphocyte counts. Pediatric cases with worse steatosis showed high P/P CD4+ (p = 0.023) and intralobular CD8+ (p = 0.027) and CD4+ cells (p = 0.012). In NAFLD cases, the lymphocyte liver infiltrate composition differs between histological areas. Treg and Th17 balance seems to condition damage progression, denoting their important role in pathogenesis.
description Fil: Bertot, Gustavo. Instituto Universitario de Ciencias de la Salud. Fundación Barceló; Argentina.
publishDate 2021
dc.date.none.fl_str_mv 2021-07-02
2025-07-11T23:46:23Z
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv https://repositorio.barcelo.edu.ar/greenstone/collect/investig/index/assoc/HASH37b2.dir/BRC_122_MED_BA.pdf
http://repositorio.barcelo.edu.ar/greenstone/collect/investig/index/assoc/HASH37b2.dir/BRC_122_MED_BA.pdf
url https://repositorio.barcelo.edu.ar/greenstone/collect/investig/index/assoc/HASH37b2.dir/BRC_122_MED_BA.pdf
http://repositorio.barcelo.edu.ar/greenstone/collect/investig/index/assoc/HASH37b2.dir/BRC_122_MED_BA.pdf
dc.language.none.fl_str_mv eng
language eng
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Nature Portfolio Scientific Reports (2021) 11:5129
publisher.none.fl_str_mv Nature Portfolio Scientific Reports (2021) 11:5129
dc.source.none.fl_str_mv reponame:Repositorio Institucional (Fundacion Barceló)
instname:Fundación H. A. Barceló
reponame_str Repositorio Institucional (Fundacion Barceló)
collection Repositorio Institucional (Fundacion Barceló)
instname_str Fundación H. A. Barceló
repository.name.fl_str_mv Repositorio Institucional (Fundacion Barceló) - Fundación H. A. Barceló
repository.mail.fl_str_mv lrodriguezares@barcelo.edu.ar
_version_ 1846787622788136960
score 12.471625