Murph J R, Grose C, McAndrew P, Mickiewicz C, Mento S, Cano F, Radick L, Ritchey M, Stout M G
Department of Pediatrics, University of Iowa College of Medicine, Iowa City, IA.
Pediatr Infect Dis J. 1988 Nov;7(11):760-5. doi: 10.1097/00006454-198811000-00003.
The most widely used poliovaccine in the United States contains the three live attenuated strains originally produced by Sabin. An inactivated ("killed") formulation of this trivalent polio vaccine has now been prepared. Before testing this new vaccine, we assessed the poliovirus immune status of 39 healthy adult males between the ages of 20 and 44 years and found that 69% had detectable (titer greater than or equal to 1:4) neutralizing antibody to all three types of poliovirus, whereas 31% lacked antibody to 1 or more types even though they had a history of childhood polio immunization. Of interest, the lowest levels of neutralizing antibody were found among young adults in their late 20s, 2 of whom lacked antibody to all 3 polio types. When the Sabin inactivated trivalent poliovirus vaccine was initially administered to 12 seropositive volunteers, all responded with rising titers of neutralizing antibody that persisted for at least 18 months (range, 1:249 to 1:4948). The new vaccine was also given to a second group of 9 individuals with little or no detectable neutralizing antibody to at least one poliovirus type and again all vaccinees manifested a humoral immune response to poliovirus. Except for transient local tenderness at the injection site, no untoward reactions to immunization were observed. Thus, this Phase I study (1) confirmed earlier reports that titers of poliovirus antibody may decline to undetectable levels by early adulthood and (2) demonstrated that adults previously immunized with poliovirus vaccine responded rapidly to all 3 poliovirus types (within 7 days) upon reimmunization with Sabin inactivated trivalent vaccine whether or not there was preexisting detectable antibody.
美国使用最广泛的脊髓灰质炎疫苗含有萨宾最初生产的三种减毒活毒株。现在已经制备出了这种三价脊髓灰质炎疫苗的灭活(“死”)制剂。在对这种新疫苗进行测试之前,我们评估了39名年龄在20至44岁之间的健康成年男性的脊髓灰质炎病毒免疫状态,发现69%的人对所有三种脊髓灰质炎病毒都有可检测到的(滴度大于或等于1:4)中和抗体,而31%的人即使有儿童期脊髓灰质炎免疫史,仍缺乏对1种或更多种病毒类型的抗体。有趣的是,中和抗体水平最低的是接近30岁的年轻人,其中2人缺乏对所有三种脊髓灰质炎病毒类型的抗体。当最初给12名血清阳性志愿者接种萨宾灭活三价脊髓灰质炎病毒疫苗时,所有人的中和抗体滴度都上升,并且至少持续了18个月(范围为1:249至1:4948)。新疫苗还接种给了第二组9名对至少一种脊髓灰质炎病毒几乎没有或没有可检测到的中和抗体的个体,所有接种者再次表现出对脊髓灰质炎病毒的体液免疫反应。除了注射部位短暂的局部压痛外,未观察到免疫接种的不良反应。因此,这项I期研究(1)证实了早期的报告,即脊髓灰质炎病毒抗体滴度在成年早期可能降至无法检测的水平,(2)表明以前接种过脊髓灰质炎疫苗的成年人,无论之前是否存在可检测到的抗体,在用萨宾灭活三价疫苗再次接种后,对所有三种脊髓灰质炎病毒类型都能迅速产生反应(在7天内)。