首页> 外文期刊>South African medical journal = >Immunogenicity and safety of an acellular pertussis, diphtheria, tetanus, inactivated poliovirus, Hib-conjugate combined vaccine (PentaximTM) and monovalent hepatitis B vaccine at 6, 10 and 14 weeks of age in infants in South Africa
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Immunogenicity and safety of an acellular pertussis, diphtheria, tetanus, inactivated poliovirus, Hib-conjugate combined vaccine (PentaximTM) and monovalent hepatitis B vaccine at 6, 10 and 14 weeks of age in infants in South Africa

机译:南非婴儿在6、10和14周龄时无细胞百日咳,白喉,破伤风,灭活的脊髓灰质炎病毒,Hib结合疫苗(PentaximTM)和单价乙肝疫苗的免疫原性和安全性

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OBJECTIVE: To assess the immunogenicity and safety data for a pentavalent combination vaccine containing acellular pertussis, inactivated poliovirus, and Haemophilus influenzae (Hib) polysaccharide-conjugate antigens. METHODS: A DTaP-IPV//PRP~T vaccine (PentaximTM) was given at 6, 10 and 14 weeks of age to 212 infants in South Africa. Monovalent hepatitis B vaccine was given concomitantly. Immunogenicity was assessed using seroprotection and seroconversion rates; safety was assessed by monitoring for solicited injection site and systemic adverse events, and follow-up monitoring for unsolicited adverse events and serious adverse events. RESULTS: Immunogenicity was high for each vaccine antigen, and similar to a reference study done in France using a similar (2, 3 and 4 months of age) administration schedule. After the third dose, 94.6% of participants had anti-PRP 0.15 μg/ml. The anti-PRP geometric mean antibody titre (GMT) was 2.0 μg/ml. The seroprotection rates for diphtheria and tetanus (0.01 IU/ml), poliovirus types 1, 2 and 3 (8 1/dil U) and hepatitis B were all 100%. Anti-polio GMTs were very high, 1 453, 1 699 and 2 398 (1/dil U) for types 1, 2 and 3, respectively. The seroconversion/vaccine response rates to pertussis antigens (4-fold increase in antibody concentration) were 97.5% for PT and 83.9% for FHA. CONCLUSIONS: The DTaP-IPV//PRP~T vaccine was highly immunogenic at 6, 10 and 14 weeks of age in infants in South Africa, was compatible with the monovalent hepatitis B vaccine, and was well tolerated.
机译:目的:评估包含脱细胞百日咳,灭活脊髓灰质炎病毒和流感嗜血杆菌(Hib)多糖结合抗原的五价联合疫苗的免疫原性和安全性数据。方法:DTaP-IPV // PRP〜T疫苗(PentaximTM)分别在6、10和14周龄时接种给南非的212名婴儿。同时接种乙型肝炎疫苗。使用血清保护和血清转化率评估免疫原性。通过监测所招募的注射部位和全身不良事件,以及对未经请求的不良事件和严重不良事件进行随访监测,来评估安全性。结果:每种疫苗抗原的免疫原性均很高,与在法国进行的参考研究(使用年龄分别为2、3和4个月)相似。第三次给药后,有94.6%的参与者抗PRP> 0.15μg/ ml。抗PRP几何平均抗体滴度(GMT)为2.0μg/ ml。白喉和破伤风(> 0.01 IU / ml),脊髓灰质炎病毒1型,2型和3型(> 8 1 / dil U)和乙型肝炎的血清保护率均为100%。反政策GMT非常高,类型1、2和3分别为1 453、1 699和2 398(1 / dil U)。百日咳抗原的血清转化/疫苗应答率(抗体浓度增加4倍)对于PT为97.5%,对于FHA为83.9%。结论:DTaP-IPV // PRP〜T疫苗在南非婴儿中分别在6、10和14周龄时具有高度免疫原性,与单价乙型肝炎疫苗兼容,并且具有良好的耐受性。

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