The current standard therapy for the treatment of Chronic Hepatitis C is the combination of peginterferon and ribavirin, although many patients fail to clear the virus and their retreatment options are still unsatisfactory. Thymosin 1 (T1) is an immunomodulating agent which has been proposed as complementary therapy for chronic HCV especially in the setting of difficult-to-treat patients. The aim of this study was to evaluate, in patients non responders to previous Peg-based therapy, the effect of standard antiviral therapy with or without T1 on peripheral lymphocytes subsets. Twenty-four patients, 12 receiving T1 and 12 standard therapy, were enrolled. Peripheral subpopulations were analyzed by flow cytometry. While the addition of T1 did not seem to significantly modify the T lymphocyte subpopulations, since comparable behaviors were observed in the CD4 and CD8 longitudinal evaluation, T1 produced an earlier increase of NK cells. An accurate selection of HCV patients who can benefit from immunomodulation is needed.

Immunological modifications during treatment with tymosin alpha 1 plus antiviral therapy in chronic hepatitis C

FORTINI, Cinzia;
2010

Abstract

The current standard therapy for the treatment of Chronic Hepatitis C is the combination of peginterferon and ribavirin, although many patients fail to clear the virus and their retreatment options are still unsatisfactory. Thymosin 1 (T1) is an immunomodulating agent which has been proposed as complementary therapy for chronic HCV especially in the setting of difficult-to-treat patients. The aim of this study was to evaluate, in patients non responders to previous Peg-based therapy, the effect of standard antiviral therapy with or without T1 on peripheral lymphocytes subsets. Twenty-four patients, 12 receiving T1 and 12 standard therapy, were enrolled. Peripheral subpopulations were analyzed by flow cytometry. While the addition of T1 did not seem to significantly modify the T lymphocyte subpopulations, since comparable behaviors were observed in the CD4 and CD8 longitudinal evaluation, T1 produced an earlier increase of NK cells. An accurate selection of HCV patients who can benefit from immunomodulation is needed.
2010
Grandini, E.; Cannoletta, F.; Scuteri, A.; Fortini, Cinzia; Loggi, E.; Cursaro, C.; Riili, A.; Di Donato, R.; Gramenzi, A.; Bernardi, M.; Andreone, P....espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1396077
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