Tantawichien T, Benjavongkulchai M, Limsuwan K, Khawplod P, Kaewchompoo W, Chomchey P, Sitprija V
Department of Medicine, Chulalongkorn University, and the Queen Saovabha Memorial Institute (World Health Organization Collaborating Center for Research in Rabies Pathogenesis and Prevention), the Thai Red Cross Society, Bangkok.
Clin Infect Dis. 1999 May;28(5):1100-3. doi: 10.1086/514737.
The current World Health Organization recommendation for booster vaccination of previously immunized individuals with potential exposure to rabies is two doses of vaccine intramuscularly or intradermally on days 0 and 3. We report responses to two types of postexposure treatment of healthy individuals who had received preexposure rabies vaccination 1 year previously. Group A individuals received four intradermal doses (one-fifth of the diluent volume of vaccine per dose) on day 0, and group B individuals received two intramuscular doses on days 0 and 3. Immunogenicity of the two booster regimens was assessed by titrating the amount of neutralizing antibody (Nab). We found that the booster doses of vaccine produced remarkable responses in all subjects. Nab titers of > or = 0.5 IU/mL (acceptable antibody level for protection against rabies) were detected in all subjects on day 14, and they were shown to be consistently high 1 year after the booster vaccination. We also found that the Nab titers for group A were significantly higher (two- to eightfold) than those for group B on days 5, 14, 150, and 360 after the initial booster vaccination (P < .05). Our study shows that the four-site intradermal booster regimen with use of one-fifth of the diluent volume of cell-culture rabies vaccine on day 0 is associated with a significantly higher antibody response than is the conventional booster regimen for subsequent postexposure rabies treatment of individuals who have received preexposure rabies vaccination with cell-culture rabies vaccine 1 year previously.
世界卫生组织目前针对曾接种疫苗且有潜在狂犬病暴露风险的个体进行加强免疫的建议是,于第0天和第3天肌肉注射或皮内注射两剂疫苗。我们报告了对1年前接受过暴露前狂犬病疫苗接种的健康个体的两种暴露后治疗类型的反应。A组个体在第0天接受四剂皮内注射(每剂疫苗稀释液体积的五分之一),B组个体在第0天和第3天接受两剂肌肉注射。通过滴定中和抗体(Nab)的量来评估两种加强免疫方案的免疫原性。我们发现疫苗加强剂量在所有受试者中均产生了显著反应。在第14天,所有受试者均检测到中和抗体滴度≥0.5 IU/mL(预防狂犬病的可接受抗体水平),并且在加强免疫1年后显示中和抗体滴度持续较高。我们还发现,在初次加强免疫后的第5天、第14天、第150天和第360天,A组的中和抗体滴度显著高于B组(高两至八倍)(P<0.05)。我们的研究表明,对于1年前接受过细胞培养狂犬病疫苗暴露前接种的个体,在后续暴露后狂犬病治疗中,第0天使用细胞培养狂犬病疫苗稀释液体积五分之一的四部位皮内加强免疫方案比传统加强免疫方案产生的抗体反应显著更高。