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Updated: Feb 23, 2026

Stem Cell-Derived Viral Ag-Specific T Lymphocytes Suppress HBV Replication in Mice
Published on: September 25, 2019
Hepatitis E virus-induced primary cutaneous CD30(+) T cell lymphoproliferative disorder
Vincent Mallet1, Julie Bruneau2, Julien Zuber3
1Université Paris Descartes-Sorbonne Paris Cité, Paris, France; Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpital Cochin - Port Royal, Hepatology Service, Paris, France; Institut National de la Santé et de la Recherche Médicale, Unité 1223, Institut Pasteur, Paris, France.
Hepatitis E virus (HEV) can infect skin blood vessels, causing T cell lymphoproliferative disorders. Antiviral treatment led to remission, suggesting HEV’s role in these conditions.
Area of Science:
- Virology
- Immunology
- Dermatology
Background:
- Hepatitis E virus (HEV) infection is linked to unexplained extra-hepatic manifestations, including hematological disorders.
- The mechanisms behind these HEV-associated manifestations remain unclear.
- This study investigates HEV's potential extra-hepatic tropism and its role in cutaneous T cell lymphoproliferative disorders (T-LPD).
Observation:
- A patient with CD30(+) T-LPD and chronic HEV infection was treated with ribavirin.
- HEV was detected in dermal microvascular endothelial cells of the patient's skin lesions.
- T cell analysis revealed an oligoclonal CD8(+) T cell infiltrate with a tissue-resident memory phenotype.
Findings:
- Antiviral therapy resulted in remission of the T-LPD, which was sustained after achieving a virologic response.
- HEV exhibits extra-hepatic tropism, specifically infecting dermal endothelium.
- The infiltrating T cells showed a skewed Vβ signature and an oligoclonal profile, suggesting a clonal expansion driven by HEV.
Implications:
- HEV should be considered a potential cause of lymphoproliferative disorders, particularly T-LPD involving the skin.
- HEV's extra-hepatic endothelial tropism is a key factor in its pathogenesis of T-LPD.
- Antiviral treatment may be a viable first-line therapy for HEV-associated T-LPD, offering an alternative to chemotherapy.
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