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无细胞百日咳疫苗在青少年及成人中的效力

Efficacy of an acellular pertussis vaccine among adolescents and adults.

作者信息

Ward Joel I, Cherry James D, Chang Swei-Ju, Partridge Susan, Lee Hang, Treanor John, Greenberg David P, Keitel Wendy, Barenkamp Stephen, Bernstein David I, Edelman Robert, Edwards Kathryn

机构信息

UCLA Center for Vaccine Research, Research and Education Institute, Harbor-UCLA Medical Center, David Geffen School of Medicine, UCLA, Torrance, Calif 90502, USA.

出版信息

N Engl J Med. 2005 Oct 13;353(15):1555-63. doi: 10.1056/NEJMoa050824.

Abstract

BACKGROUND

Pertussis immunization of adults may be necessary to improve the control of a rising burden of disease and infection. This trial of an acellular pertussis vaccine among adolescents and adults evaluated the incidence of pertussis, vaccine safety, immunogenicity, and protective efficacy.

METHODS

Bordetella pertussis infections and illnesses were prospectively assessed in 2781 healthy subjects between the ages of 15 and 65 years who were enrolled in a national multicenter, randomized, double-blind trial of an acellular pertussis vaccine. Subjects received either a dose of a tricomponent acellular pertussis vaccine or a hepatitis A vaccine (control) and were monitored for 2.5 years for illnesses with cough that lasted for more than 5 days. Each illness was evaluated with use of a nasopharyngeal aspirate for culture and polymerase-chain-reaction assay, and serum samples from patients in both acute and convalescent stages of illness were analyzed for changes in antibodies to nine B. pertussis antigens.

RESULTS

Of the 2781 subjects, 1391 received the acellular pertussis vaccine and 1390 received the control vaccine. The groups had similar ages and demographic characteristics, and the median duration of follow-up was 22 months. The acellular pertussis vaccine was safe and immunogenic. There were 2672 prolonged illnesses with cough, but the incidence of this nonspecific outcome did not vary between the groups, even when stratified according to age, season, and duration of cough. On the basis of the primary pertussis case definition, vaccine protection was 92 percent (95 percent confidence interval, 32 to 99 percent). Among unimmunized controls with illness, 0.7 percent to 5.7 percent had B. pertussis infection, and the percentage increased with the duration of cough. On the basis of other case definitions, the incidence of pertussis in the controls ranged from 370 to 450 cases per 100,000 person-years.

CONCLUSIONS

The acellular pertussis vaccine was protective among adolescents and adults, and its routine use might reduce the overall disease burden and transmission to children.

摘要

背景

成人百日咳免疫接种对于改善日益加重的疾病和感染负担的控制可能是必要的。这项针对青少年和成人的无细胞百日咳疫苗试验评估了百日咳的发病率、疫苗安全性、免疫原性和保护效力。

方法

在一项全国性多中心、随机、双盲的无细胞百日咳疫苗试验中,对2781名年龄在15至65岁之间的健康受试者进行了前瞻性评估,观察百日咳博德特氏菌感染和疾病情况。受试者分别接种一剂三组分无细胞百日咳疫苗或甲型肝炎疫苗(对照),并对持续咳嗽超过5天的疾病进行了2.5年的监测。对每一例疾病均使用鼻咽抽吸物进行培养和聚合酶链反应检测,并分析疾病急性期和恢复期患者血清样本中针对9种百日咳博德特氏菌抗原的抗体变化。

结果

2781名受试者中,1391人接种了无细胞百日咳疫苗,1390人接种了对照疫苗。两组年龄和人口统计学特征相似,随访时间中位数为22个月。无细胞百日咳疫苗安全且具有免疫原性。有2672例持续性咳嗽疾病,但即使按年龄、季节和咳嗽持续时间分层,该非特异性结果的发病率在两组之间也没有差异。根据主要的百日咳病例定义,疫苗保护率为92%(95%置信区间为32%至99%)。在未接种疫苗的患病对照者中,0.7%至5.7%的人感染了百日咳博德特氏菌,且该百分比随咳嗽持续时间增加。根据其他病例定义,对照组百日咳发病率为每10万人年370至450例。

结论

无细胞百日咳疫苗对青少年和成人具有保护作用,其常规使用可能会降低总体疾病负担并减少向儿童的传播。

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