Bégué P C, Grimprel E M, Giovannangeli M D, Abitbol V I
Hôpital d'Enfants Armand-Trousseau, Maladies Infectieuses et Tropicales, Paris, France.
Pediatr Infect Dis J. 1998 Sep;17(9):804-9. doi: 10.1097/00006454-199809000-00011.
The changing epidemiology of pertussis in France has emphasized the need for booster vaccinations in adolescents. Although not previously recommended because of the high reactogenicity of whole cell pertussis in children older than 2 years old, the development of less reactogenic acellular pertussis vaccines means that this recommendation may be reconsidered.
Assessment of the reactogenicity and immunogenicity of a diphtheria-tetanus-acellular pertussis-inactivated poliovirus (DTPa-IPV=Group 1) vaccine administered as the fifth dose in preadolescents in comparison with a commercial diphtheria-tetanus-inactivated poliovirus (DT-IPV) (Group 2) vaccine currently recommended for this age group.
An open, randomized study involving 115 healthy subjects ages 10 to 13 years previously vaccinated with 4 doses of diphtheria-tetanus-whole cell pertussis-IPV vaccines. Reactogenicity was assessed for 4 days postvaccination using diary cards. Immunogenicity based on antibody assays in sera taken before and 1 month postvaccination was evaluated for all vaccine antigen components.
Both vaccines showed good tolerability, local and general reactogenicity being similar. For local reactions Group 1=88.1% and Group 2=86.8%, and for general reactions Group 1=40.7% and Group 2=47.2%. Headache was the most frequent general symptom with 27.1% for DTPa-IPV and 39.6% for DT-IPV. The incidence of fever was 5.1% with DTPa-IPV and 9.4% for DT-IPV. Good immune responses were obtained against all vaccine components.
The inclusion of acellular pertussis did not significantly increase the reactogenicity of DTPa-IPV in comparison with the currently recommended DT-IPV vaccine when given as a fifth dose in preadolescents. To prevent recent resurgence of pertussis in France, this vaccine should be preferred as the booster dose of DTPa-IPV at 11 to 13 years of age as recently approved by the National Council of Hygiene of France.
法国百日咳流行病学的变化凸显了青少年加强疫苗接种的必要性。尽管由于全细胞百日咳疫苗对2岁以上儿童具有高反应原性,以前未被推荐,但低反应原性无细胞百日咳疫苗的研发意味着这一建议可能需要重新考虑。
评估白喉-破伤风-无细胞百日咳-灭活脊髓灰质炎病毒(DTPa-IPV,第1组)疫苗作为青春期前儿童第五剂接种时的反应原性和免疫原性,并与目前该年龄组推荐使用的市售白喉-破伤风-灭活脊髓灰质炎病毒(DT-IPV,第2组)疫苗进行比较。
一项开放、随机研究,纳入115名年龄在10至13岁、此前已接种4剂白喉-破伤风-全细胞百日咳-IPV疫苗的健康受试者。接种疫苗后4天使用日记卡评估反应原性。对所有疫苗抗原成分,根据接种前和接种后1个月采集的血清中的抗体检测评估免疫原性。
两种疫苗均显示出良好的耐受性,局部和全身反应原性相似。局部反应方面,第1组为88.1%,第2组为86.8%;全身反应方面,第1组为40.7%,第组为47.2%。头痛是最常见的全身症状,DTPa-IPV组为27.1%,DT-IPV组为39.6%。DTPa-IPV组发热发生率为5.1%,DT-IPV组为9.4%。所有疫苗成分均获得了良好的免疫反应。
在青春期前儿童中作为第五剂接种时,与目前推荐的DT-IPV疫苗相比,无细胞百日咳疫苗的加入并未显著增加DTPa-IPV的反应原性。为预防法国近期百日咳疫情的复发,应优先选用该疫苗作为11至13岁DTPa-IPV的加强剂量,法国国家卫生委员会最近已批准使用。