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

Author:

Osmani Zgjim1ORCID,Villanueva Martin Arreola2345,Joseph‐Chazan Jasmin2346,Beudeker Boris J.1,de Knegt Robert J.1,Chung Raymond T.7,Hacohen Nir46,Aerssens Jeroen8ORCID,Bollekens Jacques8,Janssen Harry L. A.1,Gehring Adam J.910,Lauer Georg M.3,Shalek Alex K.234,van de Werken Harmen J. G.11ORCID,Boonstra Andre1

Affiliation:

1. Department of Gastroenterology and Hepatology Erasmus University Medical Center Rotterdam the Netherlands

2. Institute for Medical Engineering and Science (IMES) Department of Chemistry and Koch Institute for Integrative Cancer Research Massachusetts Institute of Technology Cambridge Massachusetts USA

3. The Ragon Institute of Massachusetts General Hospital Massachusetts Institute of Technology and Harvard University Cambridge Massachusetts USA

4. Broad Institute of MIT and Harvard Cambridge Massachusetts USA

5. Department of Biology Massachusetts Institute of Technology Cambridge Massachusetts USA

6. Department of Immunology Harvard Medical School Boston Massachusetts USA

7. Liver Center Division of Gastroenterology and Liver Center Massachusetts General Hospital and Harvard Medical School Boston Massachusetts USA

8. Clinical Translational Science Infectious Diseases Janssen Research and Development Beerse Belgium

9. Toronto Centre for Liver Disease Toronto General Hospital Research Institute University Health Network Toronto Ontario Canada

10. Department of Immunology University of Toronto Toronto Ontario Canada

11. Department of Immunology Erasmus University Medical Center Rotterdam the Netherlands

Abstract

AbstractStudies 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.

Funder

Janssen Pharmaceutica

Stichting voor Lever- en Maag-Darm Onderzoek

Publisher

Wiley

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