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Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view
Objectives: Plasmacytoid dendritic cells (pDCs) have been shown to have a role in autoimmune diseases, but their role in Autoimmune Hepatitis (AIH) is not completely clear. In the present study, we assessed the frequency of pDCs in peripheral blood of AIH patients under long-term standard immunosupp...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9006358/ https://www.ncbi.nlm.nih.gov/pubmed/35404689 http://dx.doi.org/10.1177/20587384211068667 |
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author | dos Santos, Irene P de Assunção, Mayra T Mauch, Renan M Sandy, Natascha Silva Nolasco da Silva, Marcos Tadeu Bellomo-Brandão, Maria Angela Riccetto, Adriana Gut Lopes |
author_facet | dos Santos, Irene P de Assunção, Mayra T Mauch, Renan M Sandy, Natascha Silva Nolasco da Silva, Marcos Tadeu Bellomo-Brandão, Maria Angela Riccetto, Adriana Gut Lopes |
author_sort | dos Santos, Irene P |
collection | PubMed |
description | Objectives: Plasmacytoid dendritic cells (pDCs) have been shown to have a role in autoimmune diseases, but their role in Autoimmune Hepatitis (AIH) is not completely clear. In the present study, we assessed the frequency of pDCs in peripheral blood of AIH patients under long-term standard immunosuppressive therapy. Methods: This cross-sectional analysis enrolled 27 AIH patients and 27 healthy controls. We analyzed and compared their proportion of pDCs, CD4(+), CD8(+), γδ T cells, CD25(+) regulatory T (Treg) cells, FoxP3(+), Foxp3(+)CD39(+) Treg cells, total B (CD19(+)) cells, and plasma cells (CD38(+)) in peripheral blood using flow cytometry immunophenotyping. Results: AIH patients had a lower percentage of pDCs (median frequencies of 0.2% vs. 0.4%; p = .002) and higher expression of CD8 T cells (32.5% vs 28.6%; p = 0.008) in peripheral blood, when compared to healthy controls. We did not find statistically significant differences between the groups regarding the other cell subtypes.Conclusion: Our data suggest a persistent suppression of pDCs in AIH patients, along with increased CD8 T cell activity, years after AIH diagnosis and despite of good clinical response to treatment, thus pointing to a role of pDCs in the AIH pathogenesis. |
format | Online Article Text |
id | pubmed-9006358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-90063582022-04-14 Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view dos Santos, Irene P de Assunção, Mayra T Mauch, Renan M Sandy, Natascha Silva Nolasco da Silva, Marcos Tadeu Bellomo-Brandão, Maria Angela Riccetto, Adriana Gut Lopes Int J Immunopathol Pharmacol Original Research Article Objectives: Plasmacytoid dendritic cells (pDCs) have been shown to have a role in autoimmune diseases, but their role in Autoimmune Hepatitis (AIH) is not completely clear. In the present study, we assessed the frequency of pDCs in peripheral blood of AIH patients under long-term standard immunosuppressive therapy. Methods: This cross-sectional analysis enrolled 27 AIH patients and 27 healthy controls. We analyzed and compared their proportion of pDCs, CD4(+), CD8(+), γδ T cells, CD25(+) regulatory T (Treg) cells, FoxP3(+), Foxp3(+)CD39(+) Treg cells, total B (CD19(+)) cells, and plasma cells (CD38(+)) in peripheral blood using flow cytometry immunophenotyping. Results: AIH patients had a lower percentage of pDCs (median frequencies of 0.2% vs. 0.4%; p = .002) and higher expression of CD8 T cells (32.5% vs 28.6%; p = 0.008) in peripheral blood, when compared to healthy controls. We did not find statistically significant differences between the groups regarding the other cell subtypes.Conclusion: Our data suggest a persistent suppression of pDCs in AIH patients, along with increased CD8 T cell activity, years after AIH diagnosis and despite of good clinical response to treatment, thus pointing to a role of pDCs in the AIH pathogenesis. SAGE Publications 2022-04-11 /pmc/articles/PMC9006358/ /pubmed/35404689 http://dx.doi.org/10.1177/20587384211068667 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Article dos Santos, Irene P de Assunção, Mayra T Mauch, Renan M Sandy, Natascha Silva Nolasco da Silva, Marcos Tadeu Bellomo-Brandão, Maria Angela Riccetto, Adriana Gut Lopes Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view |
title | Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view |
title_full | Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view |
title_fullStr | Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view |
title_full_unstemmed | Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view |
title_short | Patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: A different point of view |
title_sort | patients with treated autoimmune hepatitis and persistent suppression of plasmacytoid dendritic cells: a different point of view |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9006358/ https://www.ncbi.nlm.nih.gov/pubmed/35404689 http://dx.doi.org/10.1177/20587384211068667 |
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