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Open Access

Treatment of chronic HBV hepatitis – between immune control and virological control

  • Cristina Popescu1, 2Email author,
  • Alina Lobodan1,
  • Mihaela Rădulescu1, 2,
  • Anca Negru1,
  • Violeta Molagic1,
  • Adriana Hristea1, 2,
  • Roxana Petre1,
  • Daniela Munteanu1,
  • Ruxandra Moroti1, 2,
  • Raluca Năstase1,
  • Raluca Dulamă1,
  • Cătălin Tilişcan1, 2,
  • Raluca Mihăilescu1,
  • Irina Lăpădat1,
  • Ligia Ionescu1,
  • Liliana Ion1 and
  • Victoria Aramă1, 2
BMC Infectious Diseases201414(Suppl 7):O10

https://doi.org/10.1186/1471-2334-14-S7-O10

Published: 15 October 2014

Keywords

Viral LoadVirological FailureUndetectable Viral LoadImmune ControlBase Regimen

Background

According to international guidelines, the treatment of HBV hepatitis can use both pegylated interferon (IFN) and nucleoside/nucleotide analogues with high genetic barrier (NNA). The main advantage of IFN based regimen is the possibility of immune control after a therapy with finite duration. The main advantage of NNA is the virological control during lifelong therapy. Objectives: To estimate the level of immune control after IFN therapy and the level of virological control during NNA.

Methods

Retrospective analysis of HBV infected patients treated in Third Department of Matei Bals Institute, between 2008 and 2014: group 1 – patients who finished IFN therapy and group 2 – patients who received more than 6 months of NNA.

Results

Of more than 1500 HBV infected patients monitored in our Department, 213 patients received antiviral therapy: 64 patients IFN and 149 patients, NNA. Fifty-six patients in group 1 and 129 patients from group 2 met the inclusion criteria. The demographic characteristics were: in group 1 mean age – 38.51year-old and sex ratio M:F = 1.4:1 and in group 2 mean age – 47.32 and sex ratio M:F=2.2:1. The rate of immune control (defined as HBV viral load <2000 IU/mL) in group 1 was 41%, the mean duration of follow-up was 41.21 months. Thirty-two patients from group 1 had a viral load >2000 IU/mL during the follow-up period and were subsequently treated with NNA after a mean period of 14.15 months. HBsAg loss was obtained in 6 patients (10.71%) and anti-HBs seroconversion in 3 patients (23.21%). Thirteen patients were HBeAg positive and 5 of them developed anti-HBe antibodies (38.46%). Other 2 patients had HBsAg negative at EOT but after 6 months, HBsAg was positive again. In group 2 the rate of virological control (defined as undetectable viral load) was 77.34%. In 3 cases virological failure was recorded. Of 29 patients without virological control, 24 had viral load >LLQ. The mean duration of NNA therapy was 32 months. Nineteen patients had HBeAg positive and in 5 cases (26.31%) anti-HBe seroconversion was obtained, after a mean period of 36.4 months. The mean duration until viral load was undetectable was 32 months. Only one patient registered HBsAg loss, without anti-HBs seroconversion (0.77%).

Conclusion

After IFN therapy more than 40% patients obtained immune control. This rate could be higher if response guided therapy is used. During NNA therapy the rate of virological control is almost 80% but lifelong therapy is necessary.

Authors’ Affiliations

(1)
National Institute for Infectious Diseases "Prof. Dr. Matei Balş", Bucharest, Romania
(2)
Carol Davila University of Medicine and Pharmacy, Bucharest, Romania

Copyright

© Popescu et al; licensee BioMed Central Ltd. 2014

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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