Hepatic expression of tumor necrosis factor-α and evaluation of MAPK-p38 and NFκB signaling pathways in autoimmune hepatitis.

Autoimmunity Immunohistochemistry Inflammatory Infiltrate Liver Disease

Journal

Cytokine
ISSN: 1096-0023
Titre abrégé: Cytokine
Pays: England
ID NLM: 9005353

Informations de publication

Date de publication:
17 Feb 2024
Historique:
received: 23 11 2023
revised: 12 01 2024
accepted: 06 02 2024
medline: 19 2 2024
pubmed: 19 2 2024
entrez: 18 2 2024
Statut: aheadofprint

Résumé

Autoimmune hepatitis (AIH) is a necroinflammatory disease that occurs when genetically susceptible individuals are exposed to an environmental trigger. It is a rare disease, and its epidemiological aspects are nearly unknown in Northeast Brazil. In the literature, the activation of components of the inflammatory cascade pathways, including interleukins such as TNF-α and signaling factors like MAPK-p38 and NFκB, in the pathogenesis of AIH is well described in animal models. This study evaluated, for the first time, the immunostaining of TNF-α, MAPK-p38, and NFκB in immunohistochemical analysis of liver biopsies from AIH patients. The activation of the MAPK-p38 pathway was also studied through immunoassay analysis in the peripheral blood of AIH patients. Data from medical records of 25 AIH patients were analyzed. Histological and immunohistochemical analysis of liver tissue obtained from biopsies was performed to detect NFκB, MAPK-p38, and TNF-α. Immunoassay analysis of the MAPK-p38 pathway was performed in peripheral blood from 18 AIH patients and 8 healthy volunteers. Medical record analysis showed an average age of 33.3 years, with a female predominance in a ratio of 7.3:1. Concomitance with other autoimmune diseases was observed in 36 % of patients, with thyroid disorders being the most prominent among them, and an 8 % indication for liver transplantation. In the evaluation of autoantibodies, ANA was detected in 52 %, followed by SMA at 20 %, and Anti-LKM-1 at 16 %. Liver biopsy findings were like the global literature, with interface hepatitis and lymphoplasmacytic infiltration observed. Immunohistochemical analysis showed immunostaining for NFκB, MAPK-p38, and TNF-α, corroborating the inflammatory and immunological characteristics of the disease. Immunoassay analysis in peripheral blood confirmed the activation of the MAPK-p38 signaling pathway, with a statistically significant difference between AIH patients and healthy controls. The epidemiological and histological findings of AIH in this study in Northeast Brazil were like global population data. Immunohistochemical analysis of liver tissue and immunoassay analysis in peripheral blood confirmed the activation of TNF-α and the NFκB and MAPK-p38 signaling pathways in AIH patients.

Identifiants

pubmed: 38368696
pii: S1043-4666(24)00044-9
doi: 10.1016/j.cyto.2024.156541
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

156541

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Márcia Maria Medeiros de Ataides Bezerra (M)

Graduate Program in Applied Cellular and Molecular Biology (BCMA), Brazil.

Isabela Cristina de Farias Andrade (I)

Institute of Biological Sciences, University of Pernambuco (ICB), Brazil.

Júlio Cesar Dias de Melo Silva (J)

Graduate Program in Applied Cellular and Molecular Biology (BCMA), Brazil.

Ana Clara Santos Costa (A)

Institute of Biological Sciences, University of Pernambuco (ICB), Brazil.

Raldney Ricardo Costa da Silva (R)

Department of Parasitology, Aggeu Magalhães Institute (IAM/FIOCRUZ), Brazil.

Luydson Richardison Silva Vasconcelos (L)

Department of Parasitology, Aggeu Magalhães Institute (IAM/FIOCRUZ), Brazil.

Maria de Fátima Cavalcanti Toscano Barreto (M)

Institute of Liver of Pernambuco (IFP), Brazil.

Leila Maria Moreira Beltrão Pereira (L)

Institute of Liver of Pernambuco (IFP), Brazil.

Sura Wanessa Santos Rocha (S)

Graduate Program in Applied Cellular and Molecular Biology (BCMA), Brazil; Institute of Biological Sciences, University of Pernambuco (ICB), Brazil. Electronic address: sura.rocha@upe.br.

Classifications MeSH