Rituximab-Containing Treatment Regimens May Imply a Long-Term Risk for Difficult-To-Treat Chronic Hepatitis E
Bibliographic Data
| ID | 15505757 |
|---|---|
| Authors | Marten Schulz (0000-0003-0298-0156, Charité - Universitätsmedizin Berlin, corresponding author), Paula Biedermann (Robert Koch Institute), C –Thomas Bock (0000-0002-2773-486X, Robert Koch Institute), Jörg Hofmann (0000-0003-3966-515X, Charité - Universitätsmedizin Berlin), Mira Choi (0000-0002-0286-1491, Charité - Universitätsmedizin Berlin), Frank Tacke (0000-0001-6206-0226, Charité - Universitätsmedizin Berlin), Leif G Hanitsch (0000-0002-8181-0093, Charité - Universitätsmedizin Berlin), Tobias Mueller (0000-0003-3426-5421, Charité - Universitätsmedizin Berlin) |
| Year | 2020 |
| Volume | 17 |
| Issue | 1 |
| Pages | 341-341 |
| Publication date | 2020-01-03 |
| Open Access | Yes |
| Type | ARTICLE |
| Venue | International Journal of Environmental Research and Public Health (JOURNAL) |
| Journal identifiers | ISSN: 1661-7827 • E-ISSN: 1660-4601 |
| Publisher | Multidisciplinary Digital Publishing Institute (PUBLISHER • CH) |
| DOI | 10.3390/ijerph17010341 |
| PMID | 31947836 |
| OpenAlex | W2997168386 |
| Language | EN |
| References cited | 37 |
Hepatitis E virus (HEV) infection is an emerging disease in industrialized countries which is usually characterized by a self-limited course. However, there is an increased risk of HEV persistence in immunocompromised risk populations, comprising patients following solid organ transplantation or hematological malignancies. Recently, chronic HEV infection following rituximab-containing treatment regimens has been described. Here we report five patients with chronic hepatitis E after prior rituximab therapy for various indications. We determined the immunological characteristics of these patients and analyzed the development of ribavirin (RBV) treatment failure-associated mutations in the HEV genome. One patient became chronically HEV-infected 110 months after administration of rituximab (RTX). Immunological characterization revealed that all patients exhibited significant hypogammaglobulinemia and CD4+ T cell lymphopenia. One patient permanently cleared HEV following weight-based ribavirin treatment while three patients failed to reach a sustained virological response. In depth mutational analysis confirmed the presence of specific mutations associated with RBV treatment failure in these patients. Our cases indicate that rituximab-containing treatment regimens might imply a relevant risk for persistent HEV infection even years after the last rituximab application. Moreover, we provide further evidence to prior observations suggesting that chronically HEV infected patients following RTX-containing treatment regimens might be difficult to treat
Antibody · Hepatitis C virus · Hypogammaglobulinemia · Ribavirin · Rituximab · Virus · Hepatitis B Virus Studies · Hepatitis Viruses Studies and Epidemiology · Liver Disease and Transplantation · Medicine · Immunology · Internal Medicine
| Highly cited | No |
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