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一种改良的皮内预先暴露狂犬病疫苗接种方案的免疫原性——420 名旅行者的病例系列。

The immunogenicity of a modified intradermal pre-exposure rabies vaccination schedule--a case series of 420 travelers.

机构信息

Dr Deb - The Travel Doctor, Brisbane, Queensland, Australia.

出版信息

J Travel Med. 2011 Sep-Oct;18(5):327-32. doi: 10.1111/j.1708-8305.2011.00540.x. Epub 2011 Aug 15.

Abstract

BACKGROUND

Current Australian recommendations for rabies pre-exposure vaccination involve the use of cell-culture-based rabies vaccines, which are administered via intramuscular (IM) or intradermal (ID) routes. ID vaccination is more affordable for travelers, but is only recommended if there is sufficient time to perform serology 2 to 3 weeks post-vaccination and confirm immunity prior to travel. We report the immunogenicity of a modified ID schedule that can be completed in less time than the standard ID schedule, and allow more travelers to be vaccinated prior to departure.

METHODS

Travelers were offered a modified schedule if they were unable to afford standard IM vaccinations, and did not have time to complete a standard ID course. The modified schedule consisted of two ID injections of 0.1 mL of human diploid cell rabies vaccine administered on days 0 and 7, and serology was performed to determine immune status at a time between day 21 and 28.

RESULTS

A total of 420 travelers aged between 10 and 65 years were vaccinated using the modified ID course. The overall seroconversion rate was 94.5%, with 397 travelers developing antibody levels of >0.5 IU/mL when tested at approximately 21 days post-vaccination.

CONCLUSION

The modified ID schedule used in this case series was highly effective, had similar immunogenicity to the standard ID schedule, and should be considered in travelers who are unable to complete standard IM or standard ID courses of rabies vaccines.

摘要

背景

目前澳大利亚对狂犬病暴露前预防接种的建议包括使用基于细胞培养的狂犬病疫苗,通过肌内(IM)或皮内(ID)途径给药。ID 接种对旅行者来说更负担得起,但仅在有足够的时间在接种后 2 至 3 周进行血清学检查并在旅行前确认免疫的情况下才推荐使用。我们报告了一种改良的 ID 方案的免疫原性,该方案比标准 ID 方案完成时间更短,可以让更多旅行者在出发前接种疫苗。

方法

如果旅行者无法负担标准 IM 疫苗接种费用,并且没有时间完成标准 ID 疗程,则可以选择改良方案。改良方案包括在第 0 天和第 7 天进行两次 ID 注射,每次注射 0.1 毫升人二倍体细胞狂犬病疫苗,如果在第 21 天至 28 天之间进行血清学检查以确定免疫状态,则可以进行改良方案。

结果

共有 420 名年龄在 10 至 65 岁之间的旅行者使用改良 ID 疗程进行了接种。总的血清转化率为 94.5%,大约在接种后 21 天进行检测时,有 397 名旅行者的抗体水平>0.5 IU/mL。

结论

在本病例系列中使用的改良 ID 方案非常有效,与标准 ID 方案具有相似的免疫原性,对于无法完成标准 IM 或标准 ID 狂犬病疫苗疗程的旅行者应考虑使用。

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