4.8 Article

Chronic hepatitis delta virus infection leads to functional impairment and severe loss of MAIT cells

期刊

JOURNAL OF HEPATOLOGY
卷 71, 期 2, 页码 301-312

出版社

ELSEVIER
DOI: 10.1016/j.jhep.2019.04.009

关键词

Hepatitis D; Hepatitis B; Immunology; T lymphocytes

资金

  1. Swedish Research Council
  2. Swedish Cancer Society
  3. Swedish Foundation for Strategic Research
  4. Swedish Society for Medical Research
  5. Cancer Research Foundations of Radiumhemmet
  6. Knut and Alice Wallenberg Foundation
  7. Novo Nordisk Foundation
  8. Center for Innovative Medicine at Karolinska Institutet
  9. Stockholm County Council
  10. National Institutes of Health [R01DK108350]
  11. Karolinska Institutet
  12. German Research Foundation (DFG) [1273]
  13. Federal Ministry of Education and Research (BMBF) [01KI0788]
  14. Deutsches Zentrum fur Infektionsforschung
  15. German Center for Infection Research (TTU Hepatitis)
  16. Fundacao para a Ciencia e a Tecnologia Doctoral Fellowship [SFRH/BD/85290/2012]
  17. Programa Operacional Potencial Humano-Quadro de Referencia Estrategico Nacional
  18. European Social Fund
  19. Fundação para a Ciência e a Tecnologia [SFRH/BD/85290/2012] Funding Source: FCT

向作者/读者索取更多资源

Background & Aims: Hepatitis delta virus (HDV) infection is the most severe form of viral hepatitis. Although HDV-associated liver disease is considered immune-mediated, adaptive immune responses against HDV are weak. Thus, the role of several other cell-mediated mechanisms such as those driven by mucosa-associated invariant T (MAIT) cells, a group of innate-like T cells highly enriched in the human liver, has not been extensively studied in clinical HDV infection. Methods: MAIT cells from a sizeable cohort of patients with chronic HDV were analyzed ex vivo and in vitro after stimulation. Results were compared with MAIT cells from hepatitis B virus (HBV) monoinfected patients and healthy controls. Results: Circulating MAIT cells were dramatically decreased in the peripheral blood of HDV-infected patients. Signs of decline were also observed in the liver. In contrast, only a modest decrease of circulating MAIT cells was noted in HBV monoinfection. Unsupervised high-dimensional analysis of residual circulating MAIT cells in chronic HDV infection revealed the appearance of a compound phenotype of CD38(hi)PD-1(hi)CD28(lo)-CD127(lo)PLZF(lo)Eomes(lo)Helios(lo) cells indicative of activation. Corroborating these results, MAIT cells exhibited a functionally impaired responsiveness. In parallel to MAIT cell loss, HDV-infected patients exhibited signs of monocyte activation and increased levels of proinflammatory cytokines IL-12 and IL-18. In vitro, IL-12 and IL-18 induced an activated MAIT cell phenotype similar to the one observed ex vivo in HDV-infected patients. These cytokines also promoted MAIT cell death, suggesting that they may contribute to MAIT cell activation and subsequent loss during HDV infection. Conclusions: These results suggest that chronic HDV infection engages the MAIT cell compartment causing activation, functional impairment, and subsequent progressive loss of MAIT cells as the HDV-associated liver disease progresses. Lay summary: Hepatitis delta virus (HDV) infection is the most severe form of viral hepatitis. We found that in patients with HDV, a subset of innate-like T cells called mucosa-associated invariant T cells (or MAIT cells), which are normally abundant in peripheral blood and the liver, are activated, functionally impaired and severely depleted. (C) 2019 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

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