Mphahlele M J, Shattock A G, Boner W, Quinn J, McCormick P A, Carman W F
Institute of Virology, University of Glasgow, Scotland.
Hepatology. 1997 Sep;26(3):743-6. doi: 10.1002/hep.510260329.
The pre-core variant, A1896, which switches off hepatitis B e antigen (HBeAg) production, is common in hepatitis B e antigen antibody (anti-HBe)-positive chronic hepatitis patients. It has been observed in occasional case reports of acute hepatitis. However, transmission in the absence of HBeAg-producing strains, leading to acute nonfulminant hepatitis and clearance in adults, has not been reported. Here, we show that this event can occur, further confirming that A1896 strains are "wild-type" and can lead to all the same outcomes as G1896 strains. This is in keeping with phylogenetic evidence that A1896 is transmitted independently on a large scale in the population and explains anti-HBe- positive persons who have not had an HBeAg-positive phase documented.
前核心变异体A1896可关闭乙肝e抗原(HBeAg)的产生,在乙肝e抗原抗体(抗-HBe)阳性的慢性肝炎患者中很常见。在急性肝炎的个别病例报告中也观察到过这种变异体。然而,在没有产生HBeAg的毒株的情况下发生传播,并导致成人急性非暴发性肝炎及病毒清除的情况尚未见报道。在此,我们表明这种情况是可以发生的,进一步证实A1896毒株是“野生型”,并且可以导致与G1896毒株相同的所有结果。这与系统发育证据相符,即A1896在人群中大规模独立传播,也解释了那些没有记录到HBeAg阳性阶段的抗-HBe阳性者的情况。