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白喉/破伤风/百日咳疫苗加速免疫后抗体的持续性。

Persistence of antibody after accelerated immunisation with diphtheria/tetanus/pertussis vaccine.

作者信息

Ramsay M E, Corbel M J, Redhead K, Ashworth L A, Begg N T

机构信息

PHLS Communicable Disease Surveillance Centre, Colindale, London.

出版信息

BMJ. 1991 Jun 22;302(6791):1489-91. doi: 10.1136/bmj.302.6791.1489.

Abstract

OBJECTIVE

To determine the persistence of antibody to diphtheria, tetanus, and pertussis in children receiving an accelerated schedule of primary immunisation.

DESIGN

Controlled study of antibody testing of blood samples from children immunised according to various schedules: three doses of triple vaccine completed at 8-13 calendar months, 6-7 calendar months, before 6 calendar months, or three doses followed by diphtheria/tetanus before age 2.

SETTING

Plymouth Health Authority.

SUBJECTS

129 children aged 4 years who had received three doses of diphtheria/tetanus/pertussis vaccine with or without a diphtheria/tetanus booster.

MAIN OUTCOME MEASURES

Diphtheria and tetanus antitoxin concentrations and antibody titres to pertussis toxin, filamentous haemagglutinin, and agglutinogens 2 and 3.

RESULTS

All children had protective concentrations of antitoxin to diphtheria and tetanus (greater than or equal to 0.01 IU/ml). There was no evidence of a significant difference in diphtheria or tetanus antitoxin concentrations and pertussis antibody titres in children immunised with an accelerated course (third dose of triple vaccine before 6 months) compared with those who received a longer course (third dose at 8-13 months) with no booster (geometric mean antitoxin concentration 0.411 (95% confidence interval 0.273 to 0.618) v 0.426 (0.294 to 0.616) for diphtheria and 0.358 (0.231 to 0.556) v 0.299 (0.197 to 0.453) for tetanus; geometric mean antibody titres 903 (500 to 1631) v 1386 (848 to 2266) for pertussis filamentous haemagglutinin, 179 (130 to 248) v 232 (167 to 322) for pertussis toxin, and 2002 (1276 to 3142) v 3591 (2220 to 5809) for agglutinogens 2 and 3).

CONCLUSION

Immunisation with three doses of triple vaccine at monthly intervals completed before 6 months of age probably provides adequate protection against diphtheria, tetanus, and whooping cough which will persist until the age of the preschool booster.

摘要

目的

确定接受加速初级免疫接种程序的儿童对白喉、破伤风和百日咳抗体的持久性。

设计

对按照不同接种程序免疫的儿童血样进行抗体检测的对照研究:在8至13个日历月、6至7个日历月、6个日历月之前完成三剂三联疫苗接种,或在2岁前接种三剂三联疫苗后再接种白喉/破伤风疫苗。

地点

普利茅斯卫生局。

研究对象

129名4岁儿童,他们已接种三剂白喉/破伤风/百日咳疫苗,有或没有接种白喉/破伤风加强疫苗。

主要观察指标

白喉和破伤风抗毒素浓度以及针对百日咳毒素、丝状血凝素、凝集原2和3的抗体滴度。

结果

所有儿童对白喉和破伤风的抗毒素浓度均具有保护性(大于或等于0.01 IU/ml)。与接受较长接种程序(第三剂三联疫苗在8至13个月接种)且未接种加强疫苗的儿童相比,接受加速接种程序(6个月前接种第三剂三联疫苗)的儿童在白喉或破伤风抗毒素浓度以及百日咳抗体滴度方面没有显著差异(白喉抗毒素几何平均浓度分别为0.411(95%置信区间0.273至0.618)和0.426(0.294至0.616);破伤风抗毒素几何平均浓度分别为0.358(0.231至0.556)和0.299(0.197至0.453);百日咳丝状血凝素抗体几何平均滴度分别为903(500至1631)和1386(848至2266);百日咳毒素抗体几何平均滴度分别为179(130至248)和232(167至322);凝集原2和3抗体几何平均滴度分别为2002(1276至3142)和3591(2220至5809))。

结论

在6个月龄前每月间隔接种三剂三联疫苗可能为预防白喉、破伤风和百日咳提供足够的保护,这种保护将持续到学龄前加强疫苗接种年龄。

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