Cariani E, Ravaggi A, Tanzi E, Romanò L, Fiordalisi G, Bellati G, Caccamo L, Galmarini D, Albertini A, Zanetti A
III Laboratory of Clinical Chemistry, School of Medicine, University of Brescia, Italy.
J Med Virol. 1995 Dec;47(4):410-5. doi: 10.1002/jmv.1890470419.
Immunological and genomic analysis of the "a" determinant was carried out in seven patients with concurrent HBsAg and anti-HBs, four of whom were immunized against hepatitis B virus at liver transplant, two with histologically characterized chronic hepatitis B virus infection, and one HBsAg healthy carrier. The immune reactivity of the HBsAg "a" determinant was evaluated by binding to specific monoclonal antibodies, and the corresponding genomic sequence was studied by differential hybridization in microtiter plates and nucleotide sequence analysis. A double mutation generating an amino acid change (glycine to lysine) at residue 145, able to impair recognition by monoclonal antibodies, was observed in the post-transplant serum from one patient. No significant alteration of the "a" determinant sequence or reactivity was detected in the other patients. Amino acid residue 145 appears therefore to be critical for the recognition by anti-HBs antibodies. A previously undescribed glycine to lysine substitution at this level interferes with the immune reactivity of the "a" determinant.
对7例同时存在乙肝表面抗原(HBsAg)和乙肝表面抗体(抗-HBs)的患者进行了“a”决定簇的免疫学和基因组分析,其中4例在肝移植时接种了乙肝疫苗,2例为组织学确诊的慢性乙肝病毒感染患者,1例为HBsAg健康携带者。通过与特异性单克隆抗体结合评估HBsAg“a”决定簇的免疫反应性,并通过微量滴定板中的差异杂交和核苷酸序列分析研究相应的基因组序列。在1例患者移植后的血清中观察到一个双突变,该突变在第145位残基处产生氨基酸变化(甘氨酸变为赖氨酸),能够削弱单克隆抗体的识别能力。在其他患者中未检测到“a”决定簇序列或反应性的显著改变。因此,第145位氨基酸残基似乎对抗-HBs抗体的识别至关重要。在此位置上以前未描述的甘氨酸到赖氨酸的取代会干扰“a”决定簇的免疫反应性。