Ehata T, Yokosuka O, Omata M
First Department of Medicine, Chiba University School of Medicine.
Nihon Rinsho. 1993 Feb;51(2):281-5.
Infection with hepatitis B virus leads to a wide spectrum of liver injury, including self-limited acute hepatitis, fulminant hepatitis and chronic hepatitis with progression to cirrhosis or acute exacerbation to liver failure, as well as, an asymptomatic chronic carrier state. To investigate why an extreme immunological attack occurs in fulminant hepatitis and severe exacerbation, the entire precore and core region were sequenced in 13 subjects. No significant change was noted in the 6 self-limited acute hepatitis patients. In contrast, clustering changes in a small segment of core codons #84 to #99 were found in all 7 fulminant and severe exacerbation patients. These data suggest that this mutation clustering region may play an important role in the pathogenesis, and such mutations appear to be related to severe liver damage.
感染乙肝病毒会导致多种肝脏损伤,包括自限性急性肝炎、暴发性肝炎、进展为肝硬化或急性加重至肝衰竭的慢性肝炎,以及无症状慢性携带状态。为了探究为何在暴发性肝炎和严重加重时会发生极端免疫攻击,对13名受试者的整个前C区和C区进行了测序。6名自限性急性肝炎患者未发现明显变化。相比之下,在所有7名暴发性和严重加重患者中均发现C区密码子#84至#99的一小段区域存在聚集性变化。这些数据表明,该突变聚集区域可能在发病机制中起重要作用,且此类突变似乎与严重肝损伤有关。