Twelve children with chronic non-A, non-B hepatitis were entered in a pilot trial of recombinant interferon-alpha. Although all the children had hepatitis C virus RNA in serum, only five had antibodies against this virus. Children received 3 MU/m2 body surface area interferon-alpha 3 times/wk for 6
Treatment with recombinant α-interferon of chronic hepatitis C in anti-HIV-positive patients
✍ Scribed by Eduardo Marriott; Sonia Navas; Jorge Del Romero; Soledad Garcia; Inmaculada Castillo; Juan Antonio Quiroga; Dr. Vicente Carreño
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 515 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0146-6615
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✦ Synopsis
Abstract
A pilot study of chronic hepatitis C treatment was conducted in 14 patients (13 had chronic active hepatitis and 1 had liver cirrhosis). All patients were asymptomatic for the human immunodeficiency virus (HIV) type 1 (mean CD4 count of 584 ± 283 cells/mm^3^). Patients received 9 MU rlFN‐α2A per day for three months. After this, patients received 9 MU three times weekly for three months, 6 MU for another three months on the same protocol, and finally 3 MU again three times weekly for the last three months. After the first month of ALT treatment in 9 patients (64%) returned to normal; a significant decrease in ALT levels was observed with respect to the pretreatment values (mean of 42 lU/l, range 15–75 vs 152 IUI, range 69–355; P < 0.01). Of the 9 patients who completed the treatment period, 5 had a complete response, and 4 of these 5 continued with normal ALT values during follow‐up (sustained response) while the other patient relapsed within one month after cessation of therapy. The remaining 4 patients were non‐responders (including one case with a break‐through of the response). HCV‐RNA was not detectable in 3 of the 5 responders at the end of therapy while during follow‐up viral RNA became undetectable in the other 2 patients. 2/4 non‐responder patients had detectable HCV‐RNA during follow‐up. Liver histology improved in all the patients. No changes were observed in the immunological status or HIV infection. © 1993 Wiley‐Liss, Inc.
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