Hepatitis C virus entry and glucocorticosteroids

Samira Fafi-Kremer 1,2,3, François Habersetzer 1,2,4, Thomas F. Baumert 1,2,4

Received 5 July 2010; accepted 8 July 2010. published online 18 August 2010.
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COMMENT ON:
Ciesek S, Steinmann E, Iken M, Ott M, Helfritz FA, Wappler I et al. Glucocorticosteroids increase cell entry by hepatitis C virus. Gastroenterology 2010;138:1875–84.

Background & Aims
Corticosteroids are used as immunosuppressants in patients with autoimmune disorders and transplant recipients. However, these drugs worsen hepatitis C virus (HCV) recurrence after liver transplantation, suggesting that they may directly exacerbate HCV infection.

Methods
The influence of immunosuppressive drugs on HCV replication, assembly, and entry was assessed in Huh-7.5 cells and primary human hepatocytes using cell culture- and patient-derived HCV. Replication was quantified by immunofluorescence, luciferase assays, quantitative reverse-transcriptase polymerase chain reaction, or core enzyme-linked immunosorbent assays. Expression of HCV entry factors was evaluated by cell sorting and immunoblot analyses.

Results
Glucocorticosteroids slightly reduced HCV RNA replication but increased efficiency of HCV entry by up to 10-fold. This was independent of HCV genotype but specific to HCV because vesicular stomatitis virus glycoprotein-dependent infection was not affected by these drugs. The increase in HCV entry was accompanied by up-regulation of messenger RNA and protein levels of occludin and the scavenger receptor class B type I – 2 host cell proteins required for HCV infection; increase of entry by glucocorticosteroids was ablated by RU-486, an inhibitor of glucocorticosteroid signaling. Glucocorticosteroids increased propagation of cell culture-derived HCV approximately 5- to 10-fold in partially differentiated human hepatoma cells and increased infection of primary human hepatocytes by cell culture- and patient-derived HCV.

Conclusions
Glucocorticosteroids specifically increase HCV entry by up-regulating the cell entry factors occludin and scavenger receptor class B type I. Our data suggest that the potential effects of high-dose glucocorticosteroids on HCV infection in vivo may be due to increased HCV dissemination [Reprinted with permission of the publisher].

Abbreviations: CLDN1, claudin-1, HCV, hepatitis C virus, HCVcc, cell culture-derived HCV, HCVpp, HCV pseudoparticles, LDLR, low-density lipoprotein receptor, OCLN, occludin, SR-BI, scavenger receptor class B type I

1 Inserm, U748, Strasbourg, France
2 Université de Strasbourg, Strasbourg, France
3 Laboratoire de Virologie, Hôpitaux Universitaires de Strasbourg, Strasbourg, France
4 Pôle Hépato-digestif, Hôpitaux Universitaires de Strasbourg, Strasbourg, France

Corresponding author. Address: Inserm U748, Université de Strasbourg, 3 rue Koeberlé, F-67000 Strasbourg, France. Tel.: +33 3 68 85 37 03; fax: +33 3 68 85 37 24.

PII: S0168-8278(10)00701-4
doi:10.1016/j.jhep.2010.07.007
© 2010 Published by Elsevier Inc.

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