Leroux-Roels G, Desombere I, De Tollenaere G, Petit M A, Desmons P, Hauser P, Delem A, De Grave D, Safary A
Department of Clinical Chemistry, University of Gent, Belgium.
Vaccine. 1997 Nov;15(16):1724-31. doi: 10.1016/s0264-410x(97)00117-5.
The safety and immunogenicity of a yeast-derived recombinant hepatitis B virus (HBV) vaccine containing surface antigen (S) and selected preS1 and preS2 sequences (S-L*) were compared with those of a vaccine prepared with S alone (Engerix-B). S-L* consisted of composite particles containing S and L* at a ratio of 70/30. L* encompassed amino acid residues 12-52 of preS1 residues 133-145 of preS2, and the entire S domain. A total of 100 healthy, HBV-seronegative, young adults were randomized to receive 20 micrograms/dose of either S-L* or Engerix-B under double-blind conditions according to a 0-, 1-, 2-, 12-month schedule. In vivo humoral and in vitro lymphoproliferative responses to S and preS regions were monitored. Addition of the selected preS sequences to S did not enhance the in vivo humoral anti-HBs response but improved the in vitro stimulating capacity of the antigen (L*) in S-L* primed subjects.
将含有表面抗原(S)以及选定的前S1和前S2序列(S-L*)的酵母重组乙型肝炎病毒(HBV)疫苗的安全性和免疫原性,与仅用S制备的疫苗(Engerix-B)进行了比较。S-L由含有S和L且比例为70/30的复合颗粒组成。L包含前S1的12至52位氨基酸残基、前S2的133至145位氨基酸残基以及整个S结构域。总共100名健康、HBV血清学阴性的年轻人被随机分组,按照0、1、2、12个月的接种程序,在双盲条件下接受20微克/剂量的S-L或Engerix-B疫苗接种。监测了对S和前S区域的体内体液反应和体外淋巴细胞增殖反应。将选定的前S序列添加到S中并没有增强体内抗-HBs体液反应,但提高了S-L免疫的受试者体内抗原(L)的体外刺激能力。