Intrahepatic plasma cells, but not atypical memory B cells, associate with clinical phases of chronic hepatitis B

Zgjim Osmani*, Martin Arreola Villanueva, Jasmin Joseph-Chazan, Boris J Beudeker, Robert J de Knegt, Raymond T Chung, Nir Hacohen, Jeroen Aerssens, Jacques Bollekens, Harry L A Janssen, Adam J Gehring, Georg M Lauer, Alex K Shalek, Harmen J G van de Werken, Andre Boonstra*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Studies have traditionally focused on the role of T cells in chronic hepatitis B (CHB), but recent evidence supports a role for B cells. The enrichment of so-called atypical memory (AtM) B cells, which show reduced signaling and impaired differentiation, is believed to be a characteristic feature of CHB, potentially contributing to the observed dysfunctional anti-HBsAg B-cell responses. Our study, involving 62 CHB patients across clinical phases, identified AtM B cells expressing IFNLR1 and interferon-stimulated genes. Contrary to previous reports, we found relatively low frequencies of AtM B cells in the liver, comparable to peripheral blood. However, liver plasma cell frequencies were significantly higher, particularly during phases with elevated viral loads and liver enzyme levels. Liver plasma cells exhibited signs of active proliferation, especially in the immune active phase. Our findings suggest a potential role for plasma cells, alongside potential implications and consequences of local proliferation, within the livers of CHB patients. While the significance of AtM B cells remains uncertain, further investigation is warranted to determine their responsiveness to interferons and their role in CHB.

Original languageEnglish
Article number2451085
JournalEuropean Journal of Immunology
Volume54
Issue number9
Early online date30 May 2024
DOIs
Publication statusPublished - Sept 2024

Bibliographical note

Publisher Copyright:
© 2024 The Author(s). European Journal of Immunology published by Wiley-VCH GmbH.

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