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.

Development and specificities of anti-interferon neutralizing antibodies in patients with chronic hepatitis C treated with pegylated interferon-α / Scagnolari, C; Trombetti, S; Soldà, A; Milella, M; Gaeta, Gb; Angarano, G; Scotto, G; Caporaso, Nicola; Morisco, Filomena; Cozzolongo, R; Giannelli, G; Fasano, M; Santantonio, T; Antonelli, G.. - In: CLINICAL MICROBIOLOGY AND INFECTION. - ISSN 1198-743X. - STAMPA. - (2011), pp. doi: 10.1111/j.1469-0691.2011.03729.x. [Epub ahead of print]-doi: 10.1111/j.1469-0691.2011.03729.x. [Epub ahead of print]. [10.1111/j.1469-0691.2011.03729.x]

Development and specificities of anti-interferon neutralizing antibodies in patients with chronic hepatitis C treated with pegylated interferon-α.

CAPORASO, NICOLA;MORISCO, FILOMENA;
2011

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.
2011
Development and specificities of anti-interferon neutralizing antibodies in patients with chronic hepatitis C treated with pegylated interferon-α / Scagnolari, C; Trombetti, S; Soldà, A; Milella, M; Gaeta, Gb; Angarano, G; Scotto, G; Caporaso, Nicola; Morisco, Filomena; Cozzolongo, R; Giannelli, G; Fasano, M; Santantonio, T; Antonelli, G.. - In: CLINICAL MICROBIOLOGY AND INFECTION. - ISSN 1198-743X. - STAMPA. - (2011), pp. doi: 10.1111/j.1469-0691.2011.03729.x. [Epub ahead of print]-doi: 10.1111/j.1469-0691.2011.03729.x. [Epub ahead of print]. [10.1111/j.1469-0691.2011.03729.x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/456435
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