Dragunsky Eugenia M, Ivanov Alexander P, Wells Virgen R, Ivshina Anna V, Rezapkin Gennady V, Abe Shinobu, Potapova Svetlana G, Enterline Joan C, Hashizume Sou, Chumakov Konstantin M
Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, Maryland, USA.
J Infect Dis. 2004 Oct 15;190(8):1404-12. doi: 10.1086/424524. Epub 2004 Sep 20.
An assay for the evaluation of protective properties of inactivated poliovirus vaccines (IPVs) in transgenic (Tg) mice susceptible to poliovirus has been developed and optimized for type 2 IPV. This method was used to compare the immunogenicity and protective properties of experimental IPV produced from the attenuated Sabin strain (sIPV) with those of conventional IPV (cIPV) produced from the wild-type (wt) poliovirus MEF-1 strain. Modified enzyme-linked immunosorbent assays (ELISAs) were used to measure immune response in serum and saliva samples from test mice. Tg mice were vaccinated and were challenged either with wt poliovirus or virulent poliovirus derived from the vaccine strain. Compared with cIPV, sIPV induced lower levels of antibodies and did not completely protect mice against challenge with wt virus but did protect mice against challenge with the virulent vaccine-derived strain. This may be due to an 18% nucleotide difference between the MEF-1 and Sabin 2 strains, resulting in 72 amino acid substitutions and leading to antigenic dissimilarity. Immunological properties of both strains, revealed by cross-neutralization tests and ELISAs, confirmed that MEF-1 possesses broader immunogenicity than does Sabin 2. This animal model may be used for the assessment of new IPVs and of combination vaccines containing an IPV component.
已开发并优化了一种用于评估灭活脊髓灰质炎疫苗(IPV)对易感染脊髓灰质炎病毒的转基因(Tg)小鼠的保护特性的检测方法,用于2型IPV。该方法用于比较由减毒Sabin株生产的实验性IPV(sIPV)与由野生型(wt)脊髓灰质炎病毒MEF-1株生产的传统IPV(cIPV)的免疫原性和保护特性。使用改良的酶联免疫吸附测定(ELISA)来测量受试小鼠血清和唾液样本中的免疫反应。给Tg小鼠接种疫苗,然后用wt脊髓灰质炎病毒或源自疫苗株的强毒脊髓灰质炎病毒进行攻毒。与cIPV相比,sIPV诱导的抗体水平较低,不能完全保护小鼠免受wt病毒的攻毒,但能保护小鼠免受源自疫苗株的强毒株的攻毒。这可能是由于MEF-1和Sabin 2株之间存在18%的核苷酸差异,导致72个氨基酸替换,从而导致抗原性不同。通过交叉中和试验和ELISA揭示的两种毒株的免疫学特性证实,MEF-1比Sabin 2具有更广泛的免疫原性。这种动物模型可用于评估新型IPV和含有IPV成分的联合疫苗。