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根据法国疫苗接种计划,DTPa-IPV-HBV/Hib和DTPa-IPV/Hib疫苗与7价肺炎球菌结合疫苗联合作为健康婴儿的初次接种和加强接种的免疫原性和反应原性

[Immunogenicity and reactogenicity of DTPa-IPV-HBV/Hib and DTPa-IPV/Hib vaccines coadministered with 7-valent pneumococcal conjugate vaccine as primary vaccination and booster in healthy infants, according to the French vaccination calendar].

作者信息

Reinert P, Dejos V, Clyti N, Abitbol V

机构信息

Service de pédiatrie, CHI de Créteil, 40, avenue de Verdun, 94010 Créteil cedex, France.

出版信息

Arch Pediatr. 2008 Mar;15(3):263-70. doi: 10.1016/j.arcped.2007.10.014. Epub 2008 Feb 12.

Abstract

OBJECTIVE

Assessment of immunogenicity and reactogenicity of DTPa-IPV/Hib (Infanrixquinta) and DTPa-IPV-HBV/Hib (Infanrixhexa) combined vaccines coadministered in healthy infants with 7-valent pneumococcal conjugate vaccine (Prevenar), according to the current French vaccine recommendations.

METHOD

Multicenter, open label, non-controlled study performed in France. Each subject received 1 dose of DTPa-IPV-HBV/Hib combined vaccine at 2, 4 and 16-18 months of age, coadministered with conjugated pneumococcal vaccine and 1 dose of DTPa-IPV/Hib vaccine at 3 months of age coadministered with conjugated pneumococcal vaccine.

RESULTS

Among the 102 enrolled infants, 64 were analysed (10.09 weeks+/-1.22 of age; boys: 58%) in the According-To-Protocol (ATP) immunogenicity cohort. One month after the administration of the booster dose of DTPa-IPV-HBV/Hib vaccine, 93.8% of subjects had protective titres for anti-HBs antibody superior or equal to 10 mIU/ml (primary objective). Seroprotection rate against Haemophilus influenzae type b component (anti-PRP antibody >or=0.15 microg/ml) was 98.4% and the immune response for the 7-valent pneumococcal serotypes (antipneumococcal antibody >or=0,05 microg/ml) was between 98.4 and 100%. Local reactogenicity increased with the number of doses administered, but was comparable between combined vaccines and conjugated pneumococcal vaccine. The incidence of fever increased between the primary vaccination and the booster.

CONCLUSION

The immunogenicity and reactogenicity profile of DTPa-IPV-HBV/Hib and DTPa-IPV/Hib combined vaccines coadministered with conjugated pneumococcal vaccine according to the schedule recommended in the French vaccine calendar is acceptable and similar to previous reports.

摘要

目的

根据法国现行疫苗接种建议,评估在健康婴儿中联合接种吸附无细胞百白破-灭活脊髓灰质炎- b型流感嗜血杆菌结合疫苗(五联苗,Infanrixquinta)和吸附无细胞百白破-灭活脊髓灰质炎-乙肝- b型流感嗜血杆菌结合疫苗(六联苗,Infanrixhexa)与7价肺炎球菌结合疫苗(沛儿,Prevenar)的免疫原性和反应原性。

方法

在法国进行的多中心、开放标签、非对照研究。每名受试者在2、4和16 - 18月龄时各接种1剂吸附无细胞百白破-灭活脊髓灰质炎-乙肝- b型流感嗜血杆菌结合疫苗,并同时接种结合肺炎球菌疫苗;在3月龄时接种1剂吸附无细胞百白破-灭活脊髓灰质炎- b型流感嗜血杆菌结合疫苗,并同时接种结合肺炎球菌疫苗。

结果

在102名入组婴儿中,64名(年龄10.09周±1.22周;男孩占58%)纳入符合方案(ATP)免疫原性队列进行分析。在接种吸附无细胞百白破-灭活脊髓灰质炎-乙肝- b型流感嗜血杆菌结合疫苗加强剂量1个月后,93.8%的受试者抗-HBs抗体保护性滴度≥10 mIU/ml(主要目标)。b型流感嗜血杆菌成分的血清保护率(抗-PRP抗体≥0.15μg/ml)为98.4%,7价肺炎球菌血清型的免疫应答(抗肺炎球菌抗体≥0.05μg/ml)在98.4%至100%之间。局部反应原性随接种剂量数增加而升高,但联合疫苗与结合肺炎球菌疫苗之间相当。发热发生率在初次接种和加强接种之间有所增加。

结论

按照法国疫苗接种日程推荐的程序,联合接种吸附无细胞百白破-灭活脊髓灰质炎-乙肝- b型流感嗜血杆菌结合疫苗和吸附无细胞百白破-灭活脊髓灰质炎- b型流感嗜血杆菌结合疫苗与结合肺炎球菌疫苗的免疫原性和反应原性情况是可接受的,且与既往报告相似。

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