Sanz-Parra A, V Zquez B, Sobrino F, Cox S J, Ley V, Salt J S
J Gen Virol. 1999 Mar;80 ( Pt 3):671-679. doi: 10.1099/0022-1317-80-3-671.
A recombinant live vector vaccine was produced by insertion of cDNA encoding the structural proteins (P1) of foot-and-mouth disease virus (FMDV) into a replication-competent human adenovirus type 5 vaccine strain (Ad5 wt). Groups of cattle (n = 3) were immunized twice, by the subcutaneous and/or intranasal routes, with either the Ad5 wt vaccine or with the recombinant FMDV Ad5-P1 vaccine. All animals were challenged by intranasal instillation of FMDV 4 weeks after the second immunizations. In the absence of a detectable antibody response to FMDV, significant protection against viral challenge was seen in all of the animals immunized twice by the subcutaneous route with the recombinant vaccine. The observed partial protection against clinical disease was not associated with a reduction in titre of persistent FMDV infections in the oropharynx of challenged cattle.
通过将编码口蹄疫病毒(FMDV)结构蛋白(P1)的cDNA插入具有复制能力的人5型腺病毒疫苗株(Ad5 wt)中,制备了一种重组活载体疫苗。将牛群(n = 3)通过皮下和/或鼻内途径用Ad5 wt疫苗或重组FMDV Ad5-P1疫苗进行两次免疫。在第二次免疫后4周,通过鼻内滴注FMDV对所有动物进行攻毒。在对FMDV没有可检测到的抗体反应的情况下,用重组疫苗经皮下途径进行两次免疫的所有动物都表现出对病毒攻毒的显著保护作用。观察到的对临床疾病的部分保护作用与攻毒牛口咽中持续性FMDV感染滴度的降低无关。