Kark J D, Aynor Y, Peters C J
Am J Epidemiol. 1982 Nov;116(5):808-20. doi: 10.1093/oxfordjournals.aje.a113471.
A formalin-inactivated Rift Valley fever vaccine, originally produced in primary monkey kidney cells, has been used to protect laboratory workers. A trial of a modified vaccine, newly formulated in well-characterized diploid fetal rhesus lung cells, was conducted with 114 men aged 19--24 years. Of the 107 subjects who received up to three injections of 0.1 to 1 ml vaccine (an additional seven received a placebo) one had a local hypersensitivity-type reaction and another a generalized urticarial syndrome. Both cases had a prior history of hypersensitivity states. No pyrogenicity was detected and only insignificant systemic reactions were recorded. Mild and transient local reactions ranged from 5% at the lowest dose level to 43% at the highest. Serologic response, as assessed by plaque reduction neutralizing antibody titers, was dose dependent. Within a single vaccine lot tested at multiple dose levels, peak (day 42) geometric mean titers ranged from 48 (at 0.1 ml x 3) to 436 (at 1.0 ml x 3). Reciprocal titers of greater than or equal to 40 are considered to be protective. Comparison of three lots at the 0.5 ml level indicated between lot variability, though this was not statistically significant. A sharp decline in antibody titers was observed in all vaccination groups by day 84; six months after vaccination apparently protective antibody titers were present only in groups that received 1 ml x 3 and 0.5 ml x 3 of the most antigenic lot of vaccine. These results suggest that 1) the vaccine is generally nonreactogenic, but individuals with a prior history of hypersensitivity states should be observed for allergic side effects; 2) existing vaccine supplies cannot be extended by using lower dose levels without a lower and less sustained serologic response; 3) a booster dose is necessary six months or more following the primary series; 4) although the current TSI-GSD-200 vaccine is immunogenic, a more potent vaccine is needed.
一种最初在原代猴肾细胞中生产的福尔马林灭活裂谷热疫苗已被用于保护实验室工作人员。对一种新配方的改良疫苗进行了试验,该疫苗在特性明确的二倍体恒河猴胎儿肺细胞中制备,试验对象为114名年龄在19至24岁的男性。在107名接受了多达三次0.1至1毫升疫苗注射的受试者中(另外7人接受了安慰剂),1人出现局部过敏样反应,另1人出现全身性荨麻疹综合征。这两例患者既往均有过敏状态病史。未检测到热原性,仅记录到轻微的全身反应。轻度和短暂的局部反应在最低剂量水平为5%,在最高剂量水平为43%。通过蚀斑减少中和抗体滴度评估的血清学反应呈剂量依赖性。在多个剂量水平测试的单个疫苗批次中,峰值(第42天)几何平均滴度范围为48(0.1毫升×3)至436(1.0毫升×3)。大于或等于40的倒数滴度被认为具有保护作用。在0.5毫升水平对三个批次进行比较表明批次间存在差异,尽管这在统计学上不显著。到第84天,所有疫苗接种组的抗体滴度均急剧下降;接种疫苗六个月后,显然只有接受最具抗原性批次疫苗1毫升×3和0.5毫升×3的组中存在具有保护作用的抗体滴度。这些结果表明:1)该疫苗一般无反应原性,但有过敏状态病史的个体应观察是否有过敏副作用;2)现有疫苗供应不能通过使用较低剂量水平来扩大,否则血清学反应会更低且持续时间更短;3)在初次接种系列后六个月或更长时间需要加强剂量;4)尽管目前的TSI-GSD-200疫苗具有免疫原性,但仍需要一种更有效的疫苗。