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Abstract Details
Changes in serum hepatitis B surface and e antigen, IP-10, and aminotransferase levels during combination therapy of immune tolerant chronic hepatitis B
Hepatology. 2022 Feb 21. doi: 10.1002/hep.32400. Online ahead of print.
Robert P Perrillo1, Hsing-Hua S Lin2, Kathleen B Schwarz3, Philip Rosenthal4, Mauricio Lisker-Melman5, Raymond T Chung6, Ludmila Prokunina-Olsson7, Gavin Coherty8, Jordan Feld9, Hepatitis B Research Network (HBRN)
Author information
Baylor Scott and White Medical Center, Dallas, TX, USA.
Department of Epidemiology, University of Pittsburgh, Pittsburgh, PA, USA.
Johns Hopkins University School of Medicine, Baltimore, MD, USA.
University of California, San Francisco, CA, USA.
Washington University School of Medicine, St. Louis, MO, USA.
Massachusetts General Hospital, Boston, MA, USA.
National Cancer Institute, Rockville, MD, USA.
Abbott Diagnostics, Abbott Park, IL, USA.
Toronto Centre for Liver Disease, University of Toronto University Health Network, Toronto.
Abstract
Background: Treatment of immune tolerant (IT) children and adults with combined peginterferon alfa-2a and entecavir results in a decline in serum hepatitis B e antigen (HBeAg) and hepatitis B surface antigen (HBsAg) concentrations but rarely results in loss of HBeAg or sustained off-treatment response. Factors associated with declines in these viral antigens during treatment remain unexplored.
Methods: We investigated the pattern of virologic and biochemical response in 86 participants (59 children, 27 adults) by serial quantitative measurement of HBsAg (qHBsAg), quantitative HBeAg (qHBeAg), HBV RNA, interferon-inducible protein (IP-10), interleukin-18, and alanine aminotransferase (ALT). Each individual had previously been treated with 8 weeks of entecavir followed by 40 weeks of combined peginteferon and entecavir. We defined the interrelationships between these parameters and virologic response measured as nadir declines from baseline for HBeAg and HBsAg.
Results: The pattern of HBsAg and HBeAg decline were similar in pediatric and adult participants. Higher levels of IP-10 were observed during treatment in participants with greater ALT elevations and greater reductions of qHBsAg and qHBeAg. Individuals with peak ALT values exceeding 3 times the upper limit of normal were significantly more likely to have > 1 log10 decline in both viral antigens. HBV DNA became undetectable in 21 of 86 (24%) and HBV RNA in 4 of 77 (5%) during therapy, but both markers remained negative only in those who became HBsAg negative all of whom also had ALT elevations.
Conclusions: Induction of IP-10 during peginterferon treatment in adults and children in the IT phase of chronic HBV infection is associated with ALT elevations and decline in viral antigens suggesting a degree of interferon-inducible viral control.