Lu Hai-Ying, Zeng Zheng, Xu Xiao-Yuan, Zhang Nai-Lin, Yu Min, Gong Wei-Bo
Department of Infectious Diseases, Peking University First Hospital, Beijing 100034, China.
World J Gastroenterol. 2006 Jul 14;12(26):4219-23. doi: 10.3748/wjg.v12.i26.4219.
To investigate the clinical significance and presence of mutations in the surface (S) and overlapping polymerase gene of hepatitis B patients with coexisting HBsAg and anti-HBs.
Twenty-three patients with chronic hepatitis B were studied. Of the 23 patients, 11 were both positive for hepatitis B virus (HBV) surface antigen (HBsAg) and antibody to HBV surface antigen (anti-HBs), 12 were negative for anti-HBs while positive for HBsAg. DNA was extracted from 200 muL serum of the patients. Nucleotide of the surface and overlapping polymerase gene from HBV-infected patients was amplified by PCR, and the PCR products were sequenced.
Forty-one mutations were found within the surface gene protein of HBV in 15 patients (10 with coexisting HBsAg and anti-HBs). Six (14.6%) out of 41 mutations were located at "alpha " determinant region in 5 patients (4 positive for HBsAg and anti-HBs). Eleven mutations (26.8%) occurred in the downstream or upstream of "alpha " determinant region. Lamivudine (LMV)-selected mutations were found in three patients who developed anti-HBs, which occurred in amino acid positions (196, 198, 199) of the surface protein and in YMDD motif (M204I/V) of the polymerase protein simultaneously. Presence of these mutations did not relate to changes in ALT and HBV DNA levels.
Besides mutations in the "alpha " deter-minant region, mutations at downstream or upstream of the "alpha " determinant region may contribute to the development of anti-HBs. These mutations do not block the replicating competency of HBV in the presence of high titer of anti-HBs.
研究同时存在乙肝表面抗原(HBsAg)和乙肝表面抗体(抗-HBs)的乙肝患者表面(S)基因及重叠聚合酶基因的突变情况及其临床意义。
对23例慢性乙型肝炎患者进行研究。其中11例患者乙肝病毒(HBV)表面抗原(HBsAg)和乙肝表面抗原抗体(抗-HBs)均为阳性,12例患者抗-HBs阴性但HBsAg阳性。从患者200μL血清中提取DNA。采用聚合酶链反应(PCR)扩增HBV感染患者的表面及重叠聚合酶基因核苷酸,并对PCR产物进行测序。
15例患者(10例同时存在HBsAg和抗-HBs)的HBV表面基因蛋白中发现41个突变。41个突变中有6个(14.6%)位于5例患者(4例HBsAg和抗-HBs阳性)的“α”决定簇区域。11个突变(26.8%)发生在“α”决定簇区域的下游或上游。在3例出现抗-HBs的患者中发现了拉米夫定(LMV)选择的突变,这些突变同时发生在表面蛋白的氨基酸位置(196、198、199)和聚合酶蛋白的YMDD基序(M204I/V)。这些突变的存在与丙氨酸转氨酶(ALT)和HBV DNA水平的变化无关。
除“α”决定簇区域的突变外,“α”决定簇区域下游或上游的突变可能有助于抗-HBs的产生。在高滴度抗-HBs存在的情况下,这些突变不会阻断HBV的复制能力。