## Abstract A quantitative polymerase chain reaction (PCR) assay for hepatitis C viral RNA (HCVβRNA) was used to monitor viraemia levels in six patients at multiple time points before, during, and after interferon therapy for chronic nonβA, nonβB hepatitis (NANBH). Prior to therapy, serum HCVβRNA w
Interferon and chronic non-A, non-B hepatitis: Whom are we treating?
β Scribed by Harold O. Conn; Ronald L. Koretz
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 351 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0270-9139
No coin nor oath required. For personal study only.
β¦ Synopsis
Chronic hepatitis C (non-A, non-B hepatitis) is a common and often progressive viral liver diseeee. To aegees the efficacy of therapy with the antiviral agent interferon alfa, we randomly assigned 166 patients with chronic hepatitis C to treatment with either 3 million or 1 million units of recombinant interferon alfa three times weekly for 24 weeks, or to no treatment.
The probability of normalization or near normalization of the serum alanine aminotrderaee levels after six months of interferon therapy was 46 percent in patients treated with 3 million unite of interferon (P < 0.001) and 28 percent in those treated with 1 million units (P < 0.02), but only 8 percent in untreated patients. The serum alanine aminotransferase level became completely normal in 22 of the 26 patients (86 percent) who responded to treatment with 3 million units of interferon and 9 of the 16 patients (66 percent) who responded to treatment with 1 million units. The patients who received 3 million units of interferon had hietologic improvement because of the relpeeeion of lobular and periportal idlammation. Relapse within six months after the completion of treatment occumed in 51 percent of the patients treated with 3 million unite of interferon and 44 percent of those treated with 1 million units.
We conclude that a 24-week couree of interferon therapy is effective in controlling disease activity in many patients with hepatitis C, although relapse after the ceesation of treatment is common.
π SIMILAR VOLUMES
The characteristics of 86 patients with acute non-A, non-B hepatitis were compared to 23 patients with acute hepatitis A and 76 with acute hepatitis B by medical record reviews of patients seen at 5 hospitals in Baltimore, Maryland, as part of case-control study of viral hepatitis. Results of serum
Two chimpanzees with persistent non-A, non-B (NANB) hepatitis were superinfected with marmoset-passaged MS-1 HAV. Two control chimpanzees were also infected with marmoset-passaged HAV. Neither animal with persistent NANB hepatitis developed elevated alanine aminotransferase (ALT) activity, whereas b
We have conducted a multicenter randomized controlled trial comparing two doses of recombinant human a-interferon for efficacy in 60 patients with chronic non-A, non-B hepatitis. The source of infection appeared to be transfusion in 30 patients, intravenous drug abuse in 16 patients and was unknown