• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

健康成人中的无细胞百日咳疫苗:安全性与免疫原性。彭德里奇儿科协会。

An acellular pertussis vaccine in healthy adults: safety and immunogenicity. Pennridge Pediatric Associates.

作者信息

Rothstein E P, Anderson E L, Decker M D, Poland G A, Reisinger K S, Blatter M M, Jacobson R M, Mink C A, Gennevois D, Izu A E, Sinangil F, Langenberg A G

机构信息

Pennridge Pediatric Associates, Sellersville, PA 18960, USA.

出版信息

Vaccine. 1999 Aug 6;17(23-24):2999-3006. doi: 10.1016/s0264-410x(99)00164-4.

DOI:10.1016/s0264-410x(99)00164-4
PMID:10462235
Abstract

Recent data indicate that Bordetella pertussis can be an important cause of illness in adolescents and adults. In a randomized observer- and subject-blinded study, adults (> or = 18 years of age) received an acellular pertussis (aP) vaccine containing genetically inactivated pertussis toxin (PT), filamentous hemagglutinin (FHA) and pertactin (PRN), or a saline placebo, and were monitored for safety and immunogenicity. IgG antibodies to PT, FHA, and PRN were measured by enzyme-linked immunosorbent assay (ELISA) and PT neutralization by a Chinese hamster ovary (CHO) cell assay. Local reactions, more common in the aP group, were mild and transient. One month after immunization, geometric mean ELISA antibody concentrations for the aP and placebo groups, respectively, were: anti-PT, 463 and 7.6; anti-FHA, 417 and 18; and anti-PRN, 855 and 14. The anti-PT neutralization titers for the aP and placebo groups were 1:3439 and 1:58 respectively. This aP vaccine is a safe and immunogenic candidate booster vaccine against pertussis for adults.

摘要

近期数据表明,百日咳博德特氏菌可能是青少年和成人患病的一个重要原因。在一项随机、观察者和受试者双盲研究中,成年人(≥18岁)接种了一种含基因灭活百日咳毒素(PT)、丝状血凝素(FHA)和百日咳黏附素(PRN)的无细胞百日咳(aP)疫苗,或生理盐水安慰剂,并对安全性和免疫原性进行监测。通过酶联免疫吸附测定(ELISA)检测针对PT、FHA和PRN的IgG抗体,并通过中国仓鼠卵巢(CHO)细胞测定法检测PT中和情况。局部反应在aP组更为常见,症状轻微且短暂。免疫后1个月,aP组和安慰剂组的ELISA抗体几何平均浓度分别为:抗PT,463和7.6;抗FHA,417和18;抗PRN,855和14。aP组和安慰剂组的抗PT中和效价分别为1:3439和1:58。这种aP疫苗是一种安全且具有免疫原性的成人百日咳候选加强疫苗。

相似文献

1
An acellular pertussis vaccine in healthy adults: safety and immunogenicity. Pennridge Pediatric Associates.健康成人中的无细胞百日咳疫苗:安全性与免疫原性。彭德里奇儿科协会。
Vaccine. 1999 Aug 6;17(23-24):2999-3006. doi: 10.1016/s0264-410x(99)00164-4.
2
Comparison of a three-component acellular pertussis vaccine with a whole-cell pertussis vaccine in 4- through 6-year-old children. Elmwood Pediatric Associates, Pennridge Pediatric Associates.4至6岁儿童中三种无细胞百日咳疫苗与全细胞百日咳疫苗的比较。埃尔姆伍德儿科协会,彭里奇儿科协会。
Arch Pediatr Adolesc Med. 1994 May;148(5):503-7. doi: 10.1001/archpedi.1994.02170050061011.
3
Effect of priming with diphtheria and tetanus toxoids combined with whole-cell pertussis vaccine or with acellular pertussis vaccine on the safety and immunogenicity of a booster dose of an acellular pertussis vaccine containing a genetically inactivated pertussis toxin in fifteen- to twenty-one-month-old children. Italian Multicenter Group for the Study of Recombinant Acellular Pertussis Vaccine.白喉和破伤风类毒素联合全细胞百日咳疫苗或无细胞百日咳疫苗进行初次免疫,对15至21月龄儿童一剂含基因灭活百日咳毒素的无细胞百日咳疫苗加强免疫安全性和免疫原性的影响。意大利重组无细胞百日咳疫苗研究多中心小组
J Pediatr. 1995 Aug;127(2):238-43. doi: 10.1016/s0022-3476(95)70301-2.
4
Safety and immunogenicity of a combined Tetanus, Diphtheria, recombinant acellular Pertussis vaccine (TdaP) in healthy Thai adults.一种破伤风、白喉、重组无细胞百日咳联合疫苗(TdaP)在泰国健康成年人中的安全性和免疫原性。
Hum Vaccin Immunother. 2017 Jan 2;13(1):136-143. doi: 10.1080/21645515.2016.1234555. Epub 2016 Sep 29.
5
A safety and immunogenicity comparison of 12 acellular pertussis vaccines and one whole-cell pertussis vaccine given as a fourth dose in 15- to 20-month-old children.12种无细胞百日咳疫苗与1种全细胞百日咳疫苗作为第四剂,在15至20月龄儿童中接种的安全性和免疫原性比较。
Pediatrics. 1997 Nov;100(5):772-88. doi: 10.1542/peds.100.5.772.
6
Immunogenicity of a three-component acellular pertussis vaccine administered at birth.出生时接种的三组分无细胞百日咳疫苗的免疫原性。
Pediatrics. 2003 May;111(5 Pt 1):1042-5. doi: 10.1542/peds.111.5.1042.
7
Responses to primary and a booster dose of acellular, component, and whole-cell pertussis vaccines initiated at 2 months of age.对2月龄开始接种的无细胞、组分和全细胞百日咳疫苗的初次和加强剂量的反应。
Vaccine. 1996 Jun;14(9):916-22. doi: 10.1016/0264-410x(95)00257-2.
8
Immunogenicity of an acellular pertussis vaccine composed of genetically inactivated pertussis toxin combined with filamentous hemagglutinin and pertactin in infants and children.由基因灭活百日咳毒素与丝状血凝素及百日咳杆菌黏附素组成的无细胞百日咳疫苗在婴幼儿中的免疫原性。
J Pediatr. 1993 Jul;123(1):81-4. doi: 10.1016/s0022-3476(05)81543-4.
9
Assessment of safety and efficacy against Bordetella pertussis of a new tetanus-reduced dose diphtheria-acellular pertussis vaccine in a murine model.在小鼠模型中对一种新型低剂量破伤风白喉无细胞百日咳疫苗针对百日咳博德特氏菌的安全性和有效性评估。
BMC Infect Dis. 2017 Apr 4;17(1):247. doi: 10.1186/s12879-017-2369-x.
10
A phase I, randomized, controlled, dose-ranging study of investigational acellular pertussis (aP) and reduced tetanus-diphtheria-acellular pertussis (TdaP) booster vaccines in adults.一项在成人中研究新型无细胞百日咳(aP)和减少破伤风-白喉-无细胞百日咳(TdaP)加强疫苗的 I 期、随机、对照、剂量范围研究。
Hum Vaccin Immunother. 2018 Jan 2;14(1):45-58. doi: 10.1080/21645515.2017.1385686. Epub 2017 Nov 27.

引用本文的文献

1
The effectiveness and safety of pertussis booster vaccination for adolescents and adults: A systematic review and meta-analysis.青少年和成人百日咳加强疫苗接种的有效性和安全性:一项系统评价和荟萃分析。
Medicine (Baltimore). 2019 Apr;98(16):e15281. doi: 10.1097/MD.0000000000015281.
2
Pertussis serology: assessment of IgG anti-PT ELISA for replacement of the CHO cell assay.百日咳血清学:IgG 抗-PT ELISA 替代 CHO 细胞检测法的评估。
APMIS. 2010 Dec;118(12):968-72. doi: 10.1111/j.1600-0463.2010.02664.x. Epub 2010 Sep 2.
3
Acellular pertussis vaccine safety and efficacy in children, adolescents and adults.
无细胞百日咳疫苗在儿童、青少年及成人中的安全性和有效性。
Drugs. 2005;65(10):1367-89. doi: 10.2165/00003495-200565100-00005.