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Multicytokine-producing CD4+ T cells characterize the livers of patients with NASH

Authors :
Anna Woestemeier
Pasquale Scognamiglio
Yu Zhao
Jonas Wagner
Franziska Muscate
Christian Casar
Francesco Siracusa
Filippo Cortesi
Theodora Agalioti
Simone Müller
Adrian Sagebiel
Leonie Konczalla
Ramez Wahib
Karl-Frederick Karstens
Anastasios D. Giannou
Anna Duprée
Stefan Wolter
Milagros N. Wong
Anne K. Mühlig
Agata A. Bielecka
Vikas Bansal
Tianran Zhang
Oliver Mann
Victor G. Puelles
Tobias B. Huber
Ansgar W. Lohse
Jakob R. Izbicki
Noah W. Palm
Stefan Bonn
Samuel Huber
Nicola Gagliani
Source :
JCI Insight, Vol 8, Iss 1 (2023)
Publication Year :
2023
Publisher :
American Society for Clinical investigation, 2023.

Abstract

A role of CD4+ T cells during the progression from nonalcoholic fatty liver disease (NAFLD) to nonalcoholic steatohepatitis (NASH) has been suggested, but which polarization state of these cells characterizes this progression and the development of fibrosis remain unclear. In addition, a gut-liver axis has been suggested to play a role in NASH, but the role of CD4+ T cells in this axis has just begun to be investigated. Combining single-cell RNA sequencing and multiple-parameter flow cytometry, we provide the first cell atlas to our knowledge focused on liver-infiltrating CD4+ T cells in patients with NAFLD and NASH, showing that NASH is characterized by a population of multicytokine-producing CD4+ T cells. Among these cells, only those with a Th17 polarization state were enriched in patients with advanced fibrosis. In parallel, we observed that Bacteroides appeared to be enriched in the intestine of NASH patients and to correlate with the frequency of multicytokine-producing CD4+ T cells. In short, we deliver a CD4+ T cell atlas of NAFLD and NASH, providing the rationale to target CD4+ T cells with a Th17 polarization state to block fibrosis development. Finally, our data offer an early indication to test whether multicytokine-producing CD4+ T cells are part of the gut-liver axis characterizing NASH.

Subjects

Subjects :
Hepatology
Immunology
Medicine

Details

Language :
English
ISSN :
23793708
Volume :
8
Issue :
1
Database :
Directory of Open Access Journals
Journal :
JCI Insight
Publication Type :
Academic Journal
Accession number :
edsdoj.bd1ff2fbaac043e9a2e870f55d257c09
Document Type :
article
Full Text :
https://doi.org/10.1172/jci.insight.153831