Milich D R, McLachlan A, Chisari F V, Kent S B, Thorton G B
J Immunol. 1986 Jul 1;137(1):315-22.
Hepatitis B surface antigen (HBsAg) particles are composed of a major polypeptide, p25, and additional polypeptides of higher m.w., namely p33 and p39, are variably present. All three polypeptides share the 226 amino acid residues of the S region: p33 consists of the p25 sequence plus an NH2-terminal 55 residues (pre-S(2], and p39 consists of the p33 sequence plus an NH2-terminal 108-119 residues (pre-S(1). In previous studies we demonstrated the influence of two Ir genes on the humoral and cellular immune responses to the S region and identified nonresponder phenotypes (H-2f,s). Subsequent studies showed that the immune response to the pre-S(2) region was regulated by H-2-linked genes independently of the S region response, such that immunization of S region nonresponder, pre-(S2) region responder mice (H-2s) with HBsAg/p33 circumvented nonresponse to the S region. In the present study, we have extended this analysis to the pre-S(1) region of HBsAg, with the following results: 1) and pre-S(1) region is immunogenic at the T and B cell levels; 2) anti-pre-S(1) specific antibody production is regulated by H-2-linked genes and can be independent of anti-S and anti-pre-S(2) antibody production; 3) immunization of H-2f strains with HBsAg/p39 particles containing the pre-S(1) region can bypass nonresponsiveness to the S and pre-S(2) regions in terms of antibody production; 4) two synthetic peptides, p32-53 and p94-117, define murine and human antibody binding sites on the pre-S(1) region, and p1-21 and p12-32 define additional human antibody binding sites; 5) pre-S(1)-specific T cells can be elicited in S and pre-S(2) region nonresponder mice (H-2f) and provide functional T cell help for S-pre-S(2)-, and pre-S(1)-specific antibody production; and 6) a T cell recognition site in the pre-S(1) region, p12-32 was identified. These results are relevant to HBV vaccine development, and possibly to viral clearance mechanisms, since the higher m.w. polypeptides are preferentially expressed on intact virions.
乙型肝炎表面抗原(HBsAg)颗粒由一种主要多肽p25组成,另外还可能存在分子量更高的多肽,即p33和p39。所有这三种多肽都共享S区的226个氨基酸残基:p33由p25序列加上氨基末端的55个残基(前S[2])组成,p39由p33序列加上氨基末端的108 - 119个残基(前S[1])组成。在先前的研究中,我们证明了两个Ir基因对S区体液免疫和细胞免疫反应的影响,并确定了无反应表型(H - 2f,s)。随后的研究表明,对前S(2)区的免疫反应由H - 2连锁基因独立于S区反应进行调控,因此用HBsAg/p33对S区无反应、前S(2)区有反应的小鼠(H - 2s)进行免疫可避免对S区无反应。在本研究中,我们将此分析扩展到了HBsAg的前S(1)区,结果如下:1)前S(1)区在T细胞和B细胞水平具有免疫原性;2)抗前S(1)特异性抗体的产生受H - 2连锁基因调控,且可能独立于抗S和抗前S(2)抗体的产生;3)用含有前S(1)区的HBsAg/p39颗粒对H - 2f品系进行免疫,在抗体产生方面可绕过对S区和前S(2)区的无反应性;4)两种合成肽p32 - 53和p94 - 117确定了前S(1)区的小鼠和人抗体结合位点,p1 - 21和p12 - 32确定了另外的人抗体结合位点;5)在前S(1)区特异性T细胞可在前S区和前S(,2)区无反应的小鼠(H - 2f)中诱导产生,并为S - 前S(2) - 和前S(1) - 特异性抗体的产生提供功能性T细胞辅助;6)在前S(1)区确定了一个T细胞识别位点p12 - 32。这些结果与乙肝疫苗的研发相关,并且可能与病毒清除机制有关,因为分子量更高的多肽在完整病毒颗粒上优先表达。