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首页> 外文期刊>The Southeast Asian journal of tropical medicine and public health >ANTIBODY PERSISTENCE AFTER PRIMARY AND BOOSTER DOSES OF A PENTAVALENT VACCINE AGAINST DIPHTHERIA, TETANUS, ACELLULAR., PERTUSSIS, INACTIVATED POLIOVIRUS, HAEMOPHILUS INFLUENZAE TYPE B VACCINEAMONG THAI CHILDREN AT 18-19 MONTHS OF AGE
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ANTIBODY PERSISTENCE AFTER PRIMARY AND BOOSTER DOSES OF A PENTAVALENT VACCINE AGAINST DIPHTHERIA, TETANUS, ACELLULAR., PERTUSSIS, INACTIVATED POLIOVIRUS, HAEMOPHILUS INFLUENZAE TYPE B VACCINEAMONG THAI CHILDREN AT 18-19 MONTHS OF AGE

机译:对泰国儿童在18-19岁时感染双歧,破伤风,破伤风,百日咳,灭活的脊髓灰质炎,流感嗜血杆菌B型疫苗的初次和加强剂量疫苗接种后的持久性

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摘要

The World Health Organization recommends a booster dose of a pertussis-containing vaccine for children aged 1-6 years, preferably during the second year of life. This study assessed the immunogenicity and safety of a pentavalent combination vaccine containing diphtheria, tetanus, acellular pertussis, inactivated poliovirus, and conjugated-Hib polysaccharide antigens, [(DTaP-IPV//PRP~T (Pen-taxim~R)], as a booster at 18-19 months of age. Participants had received primary doses of the same vaccine at 2,4 and 6 months of age. Antibody concentrations were measured immediately before and one month after the booster dose. Adverse events were evaluated from parental reports. Geometric mean concentrations (GMCs) or titers (GMTs) decreased from post-primary to pre-booster vaccination; however, at least 94.4% of children had protective levels of anti-tetanus (>0.01 IU/ml), anti-poliovirus (>81/dil) and anti-PRP (Hib, >0.15 fig/ml) antibodies prior to the booster. Anti-diphtheria antibody titers >0.01 IU/ml were also observed in the majority of children pre-booster. One month after the booster, seroprotection rates were 99.4% for PRP (>1.0 mug/ml), 95.0% for diphtheria (>0.10 IU/ml) and 100% for tetanus (>0.1 IU/ml) and poliovirus types 1, 2, 3 (>8 1/dil). At least 93.1% of subjects had 4 fold post-booster increases in anti-pertussis antibody titers. GMCs increased from 14.0 to 307.3 EU/ml and from 13.9 to 271.9 EU/ml for anti-PT and anti-FHA, respectively. Anti-PRP GMC increased from 1.2 to 62.2 jig/ml. The booster was well tolerated. A booster dose during the second year of life was safe and induced a strong immune response, indicative of long-term protection.
机译:世界卫生组织建议对1-6岁的儿童,最好是在生命的第二年,增加剂量的含百日咳的疫苗。这项研究评估了含有白喉,破伤风,无细胞百日咳,灭活脊髓灰质炎病毒和结合型Hib多糖抗原[(DTaP-IPV // PRP〜T(Pen-taxim〜R)]的五价联合疫苗的免疫原性和安全性。在18、19个月大的时候加强免疫;参与者在2,4和6个月大时接受相同剂量的初次疫苗;在加强剂量之前和之后1个月测量抗体浓度;从父母的报告中评估不良事件几何平均浓度(GMC)或滴度(GMT)从初次接种后到加强接种前有所降低;但是,至少94.4%的儿童具有抗破伤风(> 0.01 IU / ml)和抗脊髓灰质炎病毒的保护水平(加强免疫前1个月内,大多数儿童在升压前均观察到抗白喉抗体滴度> 0.01 IU / ml,而抗白喉抗体滴度大于0.01 IU / ml。增强剂,PRP(> 1.0杯/毫升)的血清保护率为99.4%,95.0%白喉(> 0.10 IU / ml)和破伤风(> 0.1 IU / ml)和1型,2型,3型脊髓灰质炎病毒(> 8 1 / dil)为100%。至少93.1%的受试者的抗百日咳抗体滴度在加强后增加了4倍。抗PT和抗FHA的GMC分别从14.0增加到307.3 EU / ml,从13.9增加到271.9 EU / ml。抗PRP GMC从1.2升至62.2夹具/毫升。加强剂耐受性良好。在生命的第二年增加剂量是安全的,并会引起强烈的免疫反应,这表明可以长期保护。

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