Zaky D A, Douglas R G, Betts R F, Roth F K, Rinehart C J, Hogan P W
J Infect Dis. 1976 Jun;133(6):669-75. doi: 10.1093/infdis/133.6.669.
A live influenza virus candidate vaccine, "Alice" strain, was evaluated in normal healthy adults. It proved to be safe, with minimal clinical reactions. Thirteen of 21 volunteers (61.9%) with pre-existing titers of hemagglutination-inhibiting antibody of less than or equal to 1:4 and three of nine (33.3%) with initial titers of 1:8-1:16 had four-fold increases in titers of serum antibody. A second dose of vaccine did not increase the frequency or the magnitude of the serum antibody response. Nasal neutralizing antibody responses occurred in six of 18 subjects tested (38.8%). The vaccine virus appeared to produce its effect by replication since vaccine virus was recovered from six of 17 subjects (35%), administration of a vaccine inactivated by ultraviolet irradiation did not produce a response, a 1:10 dilution of virus infected two of five subjects, and a 1:100 dilution infected none of six subjects. The virus was not transmitted to the antibody-negative controls who were confined with infected volunteers. Challenge of 20 volunteers and 26 control subjects with wild-type influenza A/Udorn/307/72 (H3N2) virus revealed a significant reduction in the frequency of infection and illness among subjects who responded to "Alice" vaccine compared with the frequency among unvaccinated controls.
一种活流感病毒候选疫苗“爱丽丝”株,在正常健康成年人中进行了评估。结果证明它是安全的,临床反应极小。21名血凝抑制抗体初始滴度小于或等于1:4的志愿者中有13名(61.9%),9名初始滴度为1:8 - 1:16的志愿者中有3名(33.3%)血清抗体滴度有四倍增长。第二剂疫苗并未增加血清抗体反应的频率或幅度。在接受检测的18名受试者中有6名(38.8%)出现了鼻中和抗体反应。疫苗病毒似乎是通过复制产生效果的,因为在17名受试者中有6名(35%)检测到了疫苗病毒,接种经紫外线照射灭活的疫苗未产生反应,病毒1:10稀释液感染了5名受试者中的2名,而1:100稀释液未感染6名受试者中的任何一名。病毒未传播给与感染志愿者被隔离在一起的抗体阴性对照者。用野生型甲型/乌冬/307/72(H3N2)病毒对20名志愿者和26名对照受试者进行攻击试验发现,与未接种疫苗的对照者相比,对“爱丽丝”疫苗有反应的受试者中感染和发病的频率显著降低。