Steinhoff M C, Halsey N A, Wilson M H, Burns B A, Samorodin R K, Fries L F, Murphy B R, Clements M L
Department of International Health (Center for Immunization Research), School of Hygiene and Public Health, Johns Hopkins University, Baltimore, Maryland.
J Infect Dis. 1990 Aug;162(2):394-401. doi: 10.1093/infdis/162.2.394.
Randomized, placebo-controlled studies with 10(3)-10(7) 50% tissue-culture infectious dose (TCID50) of avian-human (ah) and cold-adapted (ca) influenza A/Bethesda/85 (H3N2) reassortant viruses were completed in 106 seronegative young children 6-48 months of age. Although the reassortants differed in six of eight RNA segments, they exhibited similar properties in level of attenuation, infectivity, immunogenicity, and efficacy. The 50% human infectious dose was 10(4.6) TCID50 for ah and 10(4.4) for ca vaccines. Both reassortants were satisfactorily attenuated with restricted replication and were no more reactogenic than placebo. The mean peak titer of virus shed was 10(1.5) (ah) to 10(2.0) (ca) TCID50/ml, and each of 37 isolates tested retained their characteristic vaccine phenotypes. Infection with ah or ca virus conferred immunity to experimental challenge with homologous virus. These findings indicate that both ah and ca influenza A/Bethesda/85 (H3N2) reassortants should be suitable vaccine candidates for use in healthy infants and young children.
在106名6至48个月大的血清阴性幼儿中完成了随机、安慰剂对照研究,研究使用了10(3)-10(7) 50%组织培养感染剂量(TCID50)的禽-人(ah)和冷适应(ca)甲型/贝塞斯达/85(H3N2)重配病毒。尽管重配病毒在八个RNA片段中的六个上存在差异,但它们在减毒水平、感染性、免疫原性和效力方面表现出相似的特性。ah疫苗的50%人感染剂量为10(4.6) TCID50,ca疫苗为10(4.4)。两种重配病毒均经充分减毒,复制受限,且反应原性不高于安慰剂。病毒排出的平均峰值滴度为10(1.5)(ah)至10(2.0)(ca)TCID50/ml,所检测的37株分离株均保留了其特征性疫苗表型。感染ah或ca病毒可使机体对同源病毒的实验性攻击产生免疫力。这些发现表明,ah和ca甲型/贝塞斯达/85(H3N2)重配病毒均应是适用于健康婴幼儿的候选疫苗。