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一种由无细胞百日咳疫苗、白喉和破伤风类毒素以及灭活脊髓灰质炎病毒疫苗组成的成人剂型疫苗,在青少年和成人中是安全且具有免疫原性的。

Adult formulation of a five component acellular pertussis vaccine combined with diphtheria and tetanus toxoids and inactivated poliovirus vaccine is safe and immunogenic in adolescents and adults.

作者信息

Halperin S A, Smith B, Russell M, Scheifele D, Mills E, Hasselback P, Pim C, Meekison W, Parker R, Lavigne P, Barreto L

机构信息

Department of Pediatrics, Dalhousie University and the IWK Grace Health Centre, Halifax, Nova Scotia, Canada.

出版信息

Pediatr Infect Dis J. 2000 Apr;19(4):276-83. doi: 10.1097/00006454-200004000-00003.

Abstract

BACKGROUND

Pertussis is increasingly recognized as an important cause of cough illness in adolescents and adults.

PURPOSE

To evaluate the safety and antibody response to a single dose of an adult formulation of a five component (pertussis toxoid, filamentous hemagglutinin, pertactin, fimbriae 2 and 3) acellular pertussis vaccine (aP) combined with diphtheria and tetanus toxoids (TdaP) and inactivated poliovirus vaccine (TdaP-IPV) in adolescents and adults and to assess the response to a second dose of the acellular pertussis vaccine in a subset of the adults.

POPULATION AND SETTING

The study addressed 1207 healthy participants (736 adults and 466 adolescents) recruited in five Canadian communities.

STUDY DESIGN

In a randomized, observer-blind, controlled clinical trial, adult participants received Td followed at a separate visit by aP, TdaP followed by IPV or TdaP-IPV; adolescents received Td-IPV followed at a separate visit by aP or TdaP-IPV. A subgroup of adults was given a booster of aP 1 month after TdaP.

OUTCOME MEASURES

Antibody titers measured before and 1 month after each immunization; adverse events enumerated at 24 h, 72 h and 8 to 10 days.

RESULTS

The aP vaccine given by itself was associated with adverse events less frequently than were Td, Td-IPV, TdaP or TdaP-IPV vaccines, but reaction rates did not differ significantly among the latter products. The antibody response against Bordetella pertussis antigens was vigorous in all groups, although adults given the TdaP-IPV vaccine had lower antibody titers against filamentous hemagglutinin, pertactin, diphtheria and tetanus antibodies than those given TdaP vaccine. Similarly adolescents given TdaP-IPV had lower antibody titers against pertussis toxin, filamentous hemagglutinin, fimbriae and agglutinins than those given Td-IPV and aP alone. A second dose of acellular pertussis vaccine was not associated with increased adverse events in adults but elicited increased antibody titers over that achieved by a single dose only against pertussis toxin.

CONCLUSIONS

This adult formulation five component aP vaccine given as TdaP-IPV is safe and immunogenic in adolescents and adults and is a candidate vaccine for adolescent and adult immunization programs.

摘要

背景

百日咳日益被认为是青少年和成人咳嗽疾病的一个重要病因。

目的

评估单剂量成人配方的五组分(百日咳毒素、丝状血凝素、百日咳杆菌黏附素、2型和3型菌毛)无细胞百日咳疫苗(aP)与白喉和破伤风类毒素(TdaP)以及灭活脊髓灰质炎病毒疫苗(TdaP-IPV)联合使用在青少年和成人中的安全性及抗体反应,并评估部分成人对第二剂无细胞百日咳疫苗的反应。

研究对象与地点

该研究涉及在加拿大五个社区招募的1207名健康参与者(736名成人和466名青少年)。

研究设计

在一项随机、观察者盲法、对照临床试验中,成年参与者接受Td,随后在另一次就诊时接受aP,或接受TdaP,随后接受IPV,或接受TdaP-IPV;青少年接受Td-IPV,随后在另一次就诊时接受aP或TdaP-IPV。一组成年亚组在接受TdaP后1个月接种一剂aP加强针。

观察指标

每次免疫接种前及接种后1个月测量抗体滴度;在24小时、72小时以及8至10天记录不良事件。

结果

单独接种aP疫苗出现不良事件的频率低于接种Td、Td-IPV、TdaP或TdaP-IPV疫苗,但后几种产品的反应率差异无统计学意义。所有组对百日咳博德特氏菌抗原的抗体反应均强烈,不过接种TdaP-IPV疫苗的成年人针对丝状血凝素、百日咳杆菌黏附素、白喉和破伤风抗体的抗体滴度低于接种TdaP疫苗的成年人。同样,接种TdaP-IPV的青少年针对百日咳毒素、丝状血凝素、菌毛和凝集素的抗体滴度低于接种Td-IPV和单独接种aP的青少年。第二剂无细胞百日咳疫苗在成人中并未增加不良事件,但仅针对百日咳毒素产生的抗体滴度高于单剂量接种时。

结论

这种作为TdaP-IPV使用的成人配方五组分aP疫苗在青少年和成人中安全且具有免疫原性,是青少年和成人免疫规划的候选疫苗。

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