首页> 外文期刊>The Pediatric infectious disease journal >Concomitant administration of a bivalent Haemophilus influenzae type b-hepatitis B vaccine, measles-mumps-rubella vaccine and varicella vaccine: safety, tolerability and immunogenicity.
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Concomitant administration of a bivalent Haemophilus influenzae type b-hepatitis B vaccine, measles-mumps-rubella vaccine and varicella vaccine: safety, tolerability and immunogenicity.

机译:并用二价乙型流感嗜血杆菌乙型肝炎疫苗,麻疹-腮腺炎-风疹疫苗和水痘疫苗:安全性,耐受性和免疫原性。

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BACKGROUND: The study was done to verify that concomitant administration of a bivalent Haemophilus influenzae type b-hepatitis B vaccine (Comvax), measles-mumps-rubella vaccine (M-M-RII) and varicella vaccine (Varivax) would be well-tolerated and suitably immunogenic with respect to all vaccine antigens. METHODS: We randomized 822 healthy 12- to 15-month-old children (1:1) to receive concomitant injections of Comvax, M-M-RII and Varivax (concomitant group) or Comvax followed 6 weeks later by injections of M-M-RII and Varivax (nonconcomitant group). Blood samples taken before and 6 weeks after vaccination were tested for antibodies to all vaccine antigens. RESULTS: Vaccinations were generally well-tolerated. Children in the concomitant and nonconcomitant treatment groups were similar with respect to the safety endpoint of primary interest (16.1 and 19.5%, respectively, had a fever > or =103 degree F rectally at any time within 14 days after either of two clinic visits). Fifteen serious adverse events were reported (eight in the concomitant group and seven in the nonconcomitant group); all resolved. Elements of two serious adverse events (fever, fever and measles-like rash; both in concomitant group children) were considered possibly related to vaccination. One child was withdrawn from the study because of a nonserious adverse event subsequently judged to be unrelated to vaccination. Similar proportions of vaccinees in the concomitant and nonconcomitant groups developed satisfactory antibody responses to the H. influenzae polysaccharide, polyribosylribitol phosphate (97.8 to 98.7%), hepatitis B surface antigen (99.2 to 100%), measles virus (99.4 to 99.6%), mumps virus (98.4 to 99.2%), rubella virus (100%) and varicella virus (93.2 to 94.6%). CONCLUSION: Concomitant administration of Comvax, M-M-RII and VARIVAX at the 12- or 15-month clinic visit is one satisfactory way of delivering some of the multiple vaccines indicated during the second year of life.
机译:背景:这项研究是为了证实同时给予二价流感嗜血杆菌b型乙型肝炎疫苗(Comvax),麻疹-腮腺炎-风疹疫苗(MM-RII)和水痘疫苗(Varivax)对所有疫苗抗原具有免疫原性。方法:我们将822名健康的12至15个月大儿童(1:1)随机接受Comvax,MM-RII和Varivax(伴随组)或Comvax的同时注射,然后在6周后注射MM-RII和Varivax (非伴随组)。测试了疫苗接种之前和之后6周的血液样本中所有疫苗抗原的抗体。结果:疫苗一般耐受良好。伴随和不伴随治疗组中的儿童在主要关注的安全终点方面相似(分别在两次就诊之后的14天内,在任何时间分别发烧> F或= 103°F,分别为16.1和19.5%) 。报告了15起严重不良事件(伴随组8例,不伴随组7例)。全部解决。认为两个严重不良事件(发烧,发烧和麻疹样皮疹;均在伴随的儿童组中)均与疫苗接种有关。由于随后发生的一次非严重不良事件被判定与疫苗接种无关,因此一名儿童退出了研究。伴随和不伴随组中相似比例的疫苗接种者对流感嗜血杆菌多糖,聚核糖核糖醇磷酸(97.8%至98.7%),乙肝表面抗原(99.2%至100%),麻疹病毒(99.4%至99.6%),腮腺炎病毒(98.4至99.2%),风疹病毒(100%)和水痘病毒(93.2至94.6%)。结论:在12或15个月的门诊就诊时同时使用Comvax,M-M-RII和VARIVAX是一种在出生后第二年提供多种疫苗的令人满意的方式。

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