Treatment of chronic delta infection with recombinant human interferon alpha 2c at high doses

Superinfection by hepatitis delta virus (HDV) in hepatitis B virus chronic carriers is normally associated with a progressive liver injury. For this reason, the aim of the present study was to determine the efficacy of recombinant interferon alpha (rIFN-α) treatment of chronic delta hepatitis, by gi...

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Veröffentlicht in:Journal of hepatology 1989-11, Vol.9 (3), p.338-344
Hauptverfasser: Porres, Juan Carlos, Carreño, Vicente, Bartolomé, Javier, Moreno, Alberto, Galiana, Fernando, Quiroga, Juan Antonio
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Sprache:eng
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Zusammenfassung:Superinfection by hepatitis delta virus (HDV) in hepatitis B virus chronic carriers is normally associated with a progressive liver injury. For this reason, the aim of the present study was to determine the efficacy of recombinant interferon alpha (rIFN-α) treatment of chronic delta hepatitis, by giving high doses of rIFN-α2c during a prolonged period. A total of 20 HBsAg, anti-HD carriers with a chronic active hepatitis were randomly allocated in two groups: (I) n = 10, control and (II) n = 10, treated with 10 MU/m 2 body surface of rIFN-α, twice weekly, intramuscularly (im) during 6 months. Basally, all patients presented HDAg in the liver and serum IgM anti-HD. Serum HDV-RNA was positive in 8 and 7 patients from groups I and II, respectively. The interferon therapy was well tolerated and all patients finished the treatment period. During the first 6 months, a decrease in ALT levels among treated patients (255 ± 98 vs. 193 ± 117) was observed. In addition, a transient drop in HDV-RNA levels was also observed. No changes in anti-HD titer, IgM anti-HD and HBsAg concentration were detected. At the end of the follow-up period (15 months) two treated patients had lost IgM anti-HD. In addition, another two patients were HDV-RNA negative. In conclusion, no permanent antiviral effects of rIFN-α2c in chronic delta hepatitis, using this schedule, was achieved.
ISSN:0168-8278
1600-0641
DOI:10.1016/0168-8278(89)90143-8