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双组分无细胞百日咳疫苗对婴儿的有效性。

Efficacy of a two-component acellular pertussis vaccine in infants.

作者信息

Liese J G, Meschievitz C K, Harzer E, Froeschle J, Hosbach P, Hoppe J E, Porter F, Stojanov S, Niinivaara K, Walker A M, Belohradsky B H

机构信息

Universitäts-Kinderklinik im Dr. v. Haunerschen Kinderspital, Munich, Germany.

出版信息

Pediatr Infect Dis J. 1997 Nov;16(11):1038-44. doi: 10.1097/00006454-199711000-00007.

Abstract

OBJECTIVE

This case-control study investigated the protective efficacy against pertussis of three doses of a two-component acellular pertussis vaccine (manufactured by Biken in Japan) combined with diphtheria and tetanus toxoids (manufactured by Connaught Laboratories in the US) in infants.

METHODS

A case-control study was performed in 63 pediatric practices in Germany. Prospective recruitment of 16,780 infants ages 6 to 17 weeks took place between February, 1993, and July, 1994. According to parental choice infants received either Biken acellular pertussis vaccine combined with diphtheria and tetanus toxoids (DTacP) (74.6%) at approximately 2, 4 and 6 months of age, or a licensed German diphtheria-tetanus toxoids-whole cell pertussis vaccine (10.9%), diphtheria-tetanus toxoids vaccine (12.5%) or no vaccine (2.0%). Prospective surveillance of pertussis cases between February, 1993, and May, 1995, was accomplished by culturing all infants < or =2 years of age presenting with cough > or = 7 days. A pertussis case was defined as any cough of 21 days or longer plus a positive Bordetella pertussis culture or household contact exposure.

RESULTS

We identified 241 pertussis cases prospectively by 11,017 B. pertussis cultures and 949 controls matched for age were selected from the same pediatric practices. Medical history and demographic and vaccine status data were collected from each case and for four controls. Data were analyzed through conditional logistic regression taking into account individual matching and adjusting for potential confounding variables. DTacP combined with diphtheria and tetanus toxoids vaccine was 82% protective (95% confidence interval, 68 to 90), diphtheria-tetanus toxoids-whole cell pertussis vaccine was 96% protective (95% confidence interval, 78 to 99). Protection against typical B. pertussis infection characterized by paroxysmal cough lasting > or =21 days was 96% (95% confidence interval, 87 to 99) for DTacP and was 97% (95% confidence interval, 79 to 100) for diphtheria-tetanus toxoids-whole cell pertussis vaccine. Adjustment for potentially confounding variables did not change the results significantly.

CONCLUSIONS

Three doses of the two-component acellular pertussis vaccine protected infants against pertussis disease during the period before the recommended booster vaccination. For typical pertussis disease as defined by the WHO efficacy was high and similar to that of a licensed German diphtheria-tetanus toxoids-whole cell pertussis vaccine.

摘要

目的

本病例对照研究调查了三剂由日本Biken公司生产的双组分无细胞百日咳疫苗与美国康诺特实验室生产的白喉和破伤风类毒素联合使用对婴儿百日咳的保护效力。

方法

在德国的63家儿科诊所开展了一项病例对照研究。1993年2月至1994年7月对16780名6至17周龄的婴儿进行了前瞻性招募。根据家长的选择,婴儿在大约2、4和6月龄时,要么接种Biken无细胞百日咳疫苗与白喉和破伤风类毒素联合疫苗(DTacP)(74.6%),要么接种德国许可的白喉-破伤风类毒素-全细胞百日咳疫苗(10.9%)、白喉-破伤风类毒素疫苗(12.5%)或不接种疫苗(2.0%)。1993年2月至1995年5月对百日咳病例进行前瞻性监测,通过培养所有出现咳嗽≥7天的≤2岁婴儿来完成。百日咳病例定义为咳嗽持续21天或更长时间加上百日咳博德特氏菌培养阳性或有家庭接触史。

结果

通过11017次百日咳博德特氏菌培养前瞻性地确定了241例百日咳病例,并从相同的儿科诊所中选取了949名年龄匹配的对照。收集了每个病例以及四名对照的病史、人口统计学和疫苗接种状态数据。通过条件逻辑回归分析数据,考虑了个体匹配并对潜在的混杂变量进行了调整。DTacP与白喉和破伤风类毒素联合疫苗的保护率为82%(95%置信区间,68至90),白喉-破伤风类毒素-全细胞百日咳疫苗的保护率为96%(95%置信区间,78至99)。针对以阵发性咳嗽持续≥21天为特征的典型百日咳博德特氏菌感染,DTacP的保护率为96%(95%置信区间,87至99),白喉-破伤风类毒素-全细胞百日咳疫苗的保护率为97%(95%置信区间,79至100)。对潜在混杂变量的调整并未显著改变结果。

结论

在推荐的加强免疫接种之前的这段时间内,三剂双组分无细胞百日咳疫苗可保护婴儿预防百日咳疾病。对于世界卫生组织定义的典型百日咳疾病,其效力很高,与德国许可的白喉-破伤风类毒素-全细胞百日咳疫苗相似。

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