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一种青少年-成人剂型的吸附破伤风和白喉类毒素与无细胞百日咳疫苗联合制剂,在4至6岁儿童中与一种儿科剂型的无细胞百日咳疫苗及吸附白喉和破伤风类毒素与灭活脊髓灰质炎疫苗联合制剂相比,具有相当的免疫原性,但反应原性较低。

An adolescent-adult formulation tetanus and diptheria toxoids adsorbed combined with acellular pertussis vaccine has comparable immunogenicity but less reactogenicity in children 4-6 years of age than a pediatric formulation acellular pertussis vaccine and diphtheria and tetanus toxoids adsorbed combined with inactivated poliomyelitis vaccine.

作者信息

Langley Joanne M, Predy Gerald, Guasparini R, Law Barbara, Diaz-Mitoma Francisco, Whitstitt Paul, Tapiero Bruce, Dionne Marc, Tomovici A, Mills Elaine, Halperin Scott A

机构信息

Department of Pediatrics, Dalhousie University, Halifax, NS, Canada.

出版信息

Vaccine. 2007 Jan 22;25(6):1121-5. doi: 10.1016/j.vaccine.2006.09.053. Epub 2006 Oct 2.

Abstract

In Canada, the fifth dose of the routine childhood immunization schedule against diphtheria, tetanus, pertussis and polio is given at 4-6 years of age. Up to 30% of children may have significant local reactions (redness, swelling) and this may be related to pertussis and diphtheria antigen content. We sought to determine if a combination product with lower content of pertussis and diphtheria toxoids (dTap) would result in fewer local reactions and not have inferior immunogenicity to a combination vaccine with higher pertussis and diphtheria content (diphtheria-tetanus-acellular pertussis-inactivated polio virus, DTaP-IPV). Healthy children aged 4-6 years with complete primary immunization series and a fourth dose of diphtheria and tetanus toxoids component pertussis inactivated polio and Haemophilus influenzae type B conjugate vaccine were randomized to one dose of dTap, followed in 4-6 weeks by one dose of IPV or control DTaP-IPV. Immediate reactions within 30 min, solicited injection site and systemic reactions within 14 days, and unsolicited adverse events (AE) within 6 weeks post-vaccination were monitored. Serum was collected prior to immunization, and 4-6 weeks after vaccine for diphtheria, tetanus and pertussis antibodies (Ab). Sample size was designed to detect > or =10% difference in injection site erythema, pain or swelling between groups 593 children at eight Canadian sites completed the study; no participant withdrew because of an AE. All safety endpoints on days 0-14 were less frequent in children randomized to the dTap than DTaP-IPV group: erythema (34.6% versus 51.7%), swelling (24.2% versus 33.8%) and pain (39.6% versus 67.2%). Fever was also less common (8.72% versus 16.9%). All children in both study groups had seroprotective Ab levels to diphtheria and tetanus at 4-6 weeks (> or =0.10 IU/mL). The majority of children in each vaccine arm had a four-fold increase in pertussis antibodies. Fever and injection site reactions are less common in 4-6 year-old-children who receive a dTap vaccine compared to DTaP-IPV, without inferior immunogenicity.

摘要

在加拿大,针对白喉、破伤风、百日咳和脊髓灰质炎的儿童常规免疫接种计划的第五剂在4至6岁时接种。高达30%的儿童可能会出现明显的局部反应(发红、肿胀),这可能与百日咳和白喉抗原含量有关。我们试图确定一种百日咳和白喉类毒素含量较低的联合疫苗(吸附无细胞百白破疫苗)是否会导致更少的局部反应,并且免疫原性不低于百日咳和白喉含量较高的联合疫苗(白喉-破伤风-无细胞百日咳-灭活脊髓灰质炎病毒疫苗,DTaP-IPV)。年龄在4至6岁、已完成基础免疫系列且接种过第四剂白喉和破伤风类毒素成分、百日咳、灭活脊髓灰质炎和B型流感嗜血杆菌结合疫苗的健康儿童被随机分为接种一剂吸附无细胞百白破疫苗组,4至6周后接种一剂脊髓灰质炎灭活疫苗,或对照组DTaP-IPV。监测接种后30分钟内的即时反应、14天内的注射部位和全身反应以及接种后6周内的非预期不良事件(AE)。在免疫接种前以及接种疫苗后4至6周采集血清,检测白喉、破伤风和百日咳抗体(Ab)。样本量设计为检测两组之间注射部位红斑、疼痛或肿胀的差异≥10%。八个加拿大地点的593名儿童完成了该研究;没有参与者因不良事件退出。在随机分配到吸附无细胞百白破疫苗组的儿童中,0至14天的所有安全终点发生率均低于DTaP-IPV组:红斑(34.6%对51.7%)、肿胀(24.2%对33.8%)和疼痛(39.6%对67.2%)。发热也较少见(8.72%对16.9%)。两个研究组的所有儿童在4至6周时对白喉和破伤风均具有血清保护性抗体水平(≥0.10 IU/mL)。每个疫苗组中的大多数儿童百日咳抗体增加了四倍。与DTaP-IPV相比,接种吸附无细胞百白破疫苗的4至6岁儿童发热和注射部位反应较少见,且免疫原性不低。

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