The polymerase chain reaction (PCR) technique has been utilized for the detection of hepatitis B virus (HBV) DNA, and several factors related to the selection of primer pairs for the PCR amplification have been demonstrated. The sensitivity of the PCR assay was compared with that of slot-blot hybrid
Incidence of hepatitis B viraemia, detected using the polymerase chain reaction, after successful therapy of hepatitis B virus carriers with interferon–α
✍ Scribed by Dr. William F. Carman; Spyros Dourakis; Peter Karayiannis; Mary Crossey; Rita Drobner; Howard C. Thomas
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 514 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0146-6615
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Thirty‐nine patients (62 sera) who, after interferon‐α therapy for chronic hepatitis B virus (HBV) infection, were seronegative for HBeAg and HBV‐DNA by dot blot hybridisation, were tested using the polymerase chain reaction (PCR) for residual viraemia. Overall, 59% of the HBsAg‐positive sera and 43% of the HBsAg‐negative sera were positive by PCR. All except one of the HBsAg‐negative patients had seroconverted to anti‐HBs. Between 13 and 18 months after therapy, 33% of the HBsAg‐positive and 20% of the HBsAg‐negative patients remained viraemic. Eighteen months after the end of treatment, no patient tested was positive. Twenty‐three patients were tested sequentially over periods from 1 to 43 months: Thirteen lost HBV‐DNA by PCR, three remained positive, five remained negative, and two patients relapsed. The merits and disadvantages of PCR for assessing interferon treatment of HBV carriers are discussed.
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