Suppr超能文献

10 年前接种过一剂破伤风、白喉、无细胞百日咳疫苗(Tdap)的成人再次接种 Tdap 的安全性和免疫原性随机对照试验。

Randomized Controlled Trial of the Safety and Immunogenicity of Revaccination With Tetanus-Diphtheria-Acellular Pertussis Vaccine (Tdap) in Adults 10 Years After a Previous Dose.

机构信息

Departments of Pediatrics and Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia.

Canadian Center for Vaccinology, Dalhousie University, IWK Health Centre, and Nova Scotia Health Authority, Halifax, Nova Scotia.

出版信息

J Pediatric Infect Dis Soc. 2019 May 11;8(2):105-114. doi: 10.1093/jpids/pix113.

Abstract

BACKGROUND

Reduced-antigen-content tetanus, diphtheria, and acellular pertussis (Tdap) vaccine is recommended in many countries for boosting immunity in adolescents and adults. Although immunity to these antigens wanes with time, currently available Tdap products are not labeled for repeat administration in the United States.

METHODS

We performed an observer-blinded, randomized controlled trial in 1330 adults aged 18 to <65 years who received either the Tdap (n = 1002) or tetanus-diphtheria (Td) (n = 328) vaccine 8 to 12 years after a dose of Tdap vaccine administered previously. Solicited adverse events following immunization were documented for 7 days after vaccination, and serious adverse events and adverse events of medical significance were documented for 6 months after vaccination. Levels of antibodies against component vaccine antigens were measured before and 1 month after vaccination.

RESULTS

A solicited adverse event was reported by 87.7% of Tdap and 88.0% of Td vaccine recipients. We found no significant differences in the rates of injection-site reactions, systemic reactions, or serious adverse events between the vaccine groups. A robust antibody response to each pertussis antigen in the Tdap-vaccinated group was found; postvaccination-to-prevaccination geometric mean antibody concentration ratios were 8:1 (pertussis toxoid), 5.9 (filamentous hemagglutinin), 6.4 (pertactin), and 5.2 (fimbriae 2 and 3). Postvaccination geometric mean concentrations of tetanus antibody (4.20 and 4.74 IU/mL, respectively) and diphtheria antibody (10.1 and 12.6 IU/mL, respectively) were similar in the Tdap and Td groups, and the rates of seroprotection against tetanus and diphtheria were >99% in both groups.

CONCLUSIONS

A second dose of Tdap vaccine in adults approximately 10 years after a previous dose was well tolerated and immunogenic. These data might facilitate consideration of providing Tdap booster doses to adults.

摘要

背景

在许多国家,含低抗原成分的破伤风、白喉和无细胞百日咳(Tdap)疫苗被推荐用于增强青少年和成人的免疫力。尽管这些抗原的免疫力会随着时间的推移而减弱,但目前在美国,Tdap 产品并未被标记用于重复给药。

方法

我们在 1330 名年龄在 18 至<65 岁的成年人中进行了一项观察者盲法、随机对照试验,这些成年人在之前接受 Tdap 疫苗接种 8 至 12 年后,分别接受 Tdap(n=1002)或破伤风白喉(Td)(n=328)疫苗。在接种疫苗后 7 天内记录疫苗接种后的不良反应,在接种疫苗后 6 个月内记录严重不良反应和有医学意义的不良反应。在接种疫苗前后测量针对疫苗成分抗原的抗体水平。

结果

Tdap 和 Td 疫苗接种者分别有 87.7%和 88.0%报告了一种不良反应。我们发现疫苗组之间在注射部位反应、全身反应或严重不良事件的发生率没有显著差异。在 Tdap 疫苗接种组中发现了针对每种百日咳抗原的强大抗体反应;接种后至接种前几何平均抗体浓度比分别为 8:1(百日咳类毒素)、5.9(丝状血凝素)、6.4( pertactin)和 5.2(fimbriae 2 和 3)。Tdap 和 Td 组的破伤风抗体(分别为 4.20 和 4.74IU/mL)和白喉抗体(分别为 10.1 和 12.6IU/mL)的接种后几何平均浓度相似,两组的破伤风和白喉血清保护率均>99%。

结论

在之前接种一剂疫苗大约 10 年后,成年人再次接种 Tdap 疫苗的耐受性良好且具有免疫原性。这些数据可能有助于考虑为成年人提供 Tdap 加强剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/607e/6510947/bd50b4d27588/pix113f0001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验