Dreesman G R, Hollinger F B, Sanchez Y, Oefinger P, Melnick J L
Infect Immun. 1981 Apr;32(1):62-7. doi: 10.1128/iai.32.1.62-67.1981.
Previous studies established that the purified polypeptides derived from the 22-nm particles associated with hepatitis B surface antigen (HBsAg) produce both humoral and cellular immunity against HBsAg in guinea pigs. Therefore, the two major polypeptides with molecular weights of 22,000 and 25,000 (P22 and P25, respectively) were isolated, adsorbed to an alum adjuvant, and used to immunize four nonimmune chimpanzees. A vigorous anti-HBs response was observed in all four animals after one inoculation of an alum-adsorbed polypeptide vaccine containing 40 micrograms of protein. After one to two booster inoculations, anti-HBs switched from being predominantly immunoglobulin M to the immunoglobin G class, indicating the establishment of immunological memory. Challenge of the vaccinated chimpanzees with 30,000 chimpanzee infectious doses of hepatitis B virus provided evidence for the efficacy of this vaccine. None of the four animals developed serological markers associated with an active hepatitis B infection, and no biochemical or histopathological changes of hepatitis were observed. A nonvaccinated control chimpanzee that was inoculated with the same hepatitis B virus material developed hepatitis B infection, confirming infectivity of the challenge inoculum.
先前的研究证实,从与乙型肝炎表面抗原(HBsAg)相关的22纳米颗粒中提取的纯化多肽,能在豚鼠体内产生针对HBsAg的体液免疫和细胞免疫。因此,分离出了分子量分别为22,000和25,000的两种主要多肽(分别为P22和P25),吸附于明矾佐剂上,用于免疫4只未免疫的黑猩猩。在接种一剂含40微克蛋白质的明矾吸附多肽疫苗后,所有4只动物均出现了强烈的抗-HBs反应。经过一到两次加强接种后,抗-HBs从主要为免疫球蛋白M转变为免疫球蛋白G类,表明建立了免疫记忆。用30,000个黑猩猩感染剂量的乙型肝炎病毒攻击接种疫苗的黑猩猩,为该疫苗的有效性提供了证据。4只动物中没有一只出现与活动性乙型肝炎感染相关的血清学标志物,也未观察到肝炎的生化或组织病理学变化。一只接种相同乙型肝炎病毒材料的未接种疫苗对照黑猩猩发生了乙型肝炎感染,证实了攻击接种物具有传染性。