ORIGINAL ARTICLE
Development and specificities of anti-interferon neutralizing antibodies in patients with chronic hepatitis C treated with pegylated interferon-α
Article first published online: 22 DEC 2011
DOI: 10.1111/j.1469-0691.2011.03729.x
© 2011 The Authors. Clinical Microbiology and Infection © 2011 European Society of Clinical Microbiology and Infectious Diseases
Additional Information
How to Cite
Scagnolari, C., Trombetti, S., Soldà, A., Milella, M., Gaeta, G. B., Angarano, G., Scotto, G., Caporaso, N., Morisco, F., Cozzolongo, R., Giannelli, G., Fasano, M., Santantonio, T. and Antonelli, G. (2012), Development and specificities of anti-interferon neutralizing antibodies in patients with chronic hepatitis C treated with pegylated interferon-α. Clinical Microbiology and Infection, 18: 1033–1039. doi: 10.1111/j.1469-0691.2011.03729.x
Publication History
- Issue published online: 10 SEP 2012
- Article first published online: 22 DEC 2011
- Accepted manuscript online: 16 NOV 2011 10:16AM EST
- Original Submission: 26 July 2011; Revised Submission: 26 October 2011; Accepted: 10 November 2011 Editor: L. Kaiser Article published online: 17 November 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- Hepatitis C virus;
- interferon;
- neutralizing antibodies;
- seroconversion;
- sustained virological response
Clin Microbiol Infect 2012; 18: 1033–1039
Abstract
Only limited data are available on the development of neutralizing antibodies (NAB) in patients with chronic hepatitis C (CHC) treated with pegylated interferon-α (PEG-IFN-α). The aim of this study was to evaluate the immunogenicity of PEG-IFN-α when administered to CHC patients who had or had not previously received standard IFN-α therapy. In addition, the specificities of NAB, together with the ability of leucocyte (LE) -IFN-α to re-establish therapeutic responsiveness in NAB-positive patients, were evaluated. NAB were assessed using a quantitative, standardized, virus-induced cytopathic effect assay. The seroconversion rate to PEG-IFN-α was higher in patients who had received previous standard IFN-α treatment than in those treated exclusively with PEG-IFN-α. Also, NAB produced during PEG-IFN-α therapy were unable to neutralize LE-IFN-α entirely, even though they can neutralize several IFN-α subtypes. In addition, the results indicate that a change to LE-IFN-α therapy can be associated with restoration of clinical responses in NAB-positive patients who had become resistant after showing an initial response to PEG-IFN-α treatment. This study emphasizes the importance of evaluating NAB development in CHC patients who become resistant to PEG-IFN-α treatment, and suggests management alternatives for patients who develop NAB.

1469-0691/asset/bannerforeground.jpg?v=1&s=d64312ac8b913a4f04c6e0a755daba751d8d8d8d)
