首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Safety and immunogenicity of concurrent administration of live attenuated influenza vaccine with measles-mumps-rubella and varicella vaccines to infants 12 to 15 months of age.
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Safety and immunogenicity of concurrent administration of live attenuated influenza vaccine with measles-mumps-rubella and varicella vaccines to infants 12 to 15 months of age.

机译:麻疹,腮腺炎,风疹和水痘疫苗同时减毒活减毒流感疫苗对12至15个月大的婴儿的安全性和免疫原性。

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OBJECTIVE: This study evaluated the safety, tolerability, and immunogenicity of live attenuated influenza vaccine administered concurrently with measles-mumps-rubella vaccine and varicella vaccine to healthy children 12 to 15 months of age. METHODS: Children were assigned randomly to receive (1) measles-mumps-rubella vaccine, varicella vaccine, and intranasal placebo on day 0, followed by 1 dose of live attenuated influenza vaccine on days 42 and 72; (2) measles-mumps-rubella, varicella, and live attenuated influenza vaccines on day 0, followed by a second dose of live attenuated influenza vaccine on day 42 and intranasally administered placebo on day 72; or (3) 1 dose of live attenuated influenza vaccine on days 0 and 42, followed by measles-mumps-rubella and varicella vaccines on day 72. Serum samples were collected before vaccination on days 0, 42, and 72. Reactogenicity events and adverse events were collected through day 41 after concurrent vaccinations and through day 10 after administration of live attenuated influenza vaccine or placebo alone. RESULTS: Among 1245 (99.5%) evaluable children, seroresponse rates and geometric mean titers for measles-mumps-rubella vaccine and varicella vaccine were similar with concurrent administration of live attenuated influenza vaccine or placebo (seroresponse rates of > or = 96% for measles-mumps-rubella vaccine and > or = 82% for varicella vaccine in both groups). Hemagglutinin-inhibiting antibody geometric mean titers and seroconversion rates to influenza strains in live attenuated influenza virus vaccine were similar after the vaccine was administered alone (seroconversion rates of 98%, 92%, and 44% for H3, B, and H1 strains, respectively) or with measles-mumps-rubella and varicella vaccines (seroconversion rates of 98%, 96%, and 43%). The incidences of reactogenicity events and adverse events were similar among treatment groups. CONCLUSIONS: Concurrent administration of live attenuated influenza vaccine with measles-mumps-rubella vaccine and varicella vaccineprovided equivalent immunogenicity, compared with separate administration, and was well tolerated.
机译:目的:本研究评估了减毒活流感疫苗与麻疹-腮腺炎-风疹疫苗和水痘疫苗同时接种对12至15个月大的健康儿童的安全性,耐受性和免疫原性。方法:将儿童随机分配在第0天接受(1)麻疹-腮腺炎-风疹疫苗,水痘疫苗和鼻内安慰剂,然后在第42和72天接受1剂减毒活流感疫苗。 (2)在第0天接种麻疹-腮腺炎-风疹,水痘和减毒活疫苗,然后在第42天接种第二剂减毒活流感疫苗,并在第72天鼻内注射安慰剂。或(3)在第0和42天接种1剂减毒活疫苗,然后在第72天接种麻疹-腮腺炎-风疹和水痘疫苗。在接种0、42和72天之前收集血清样品。在同时接种疫苗后第41天以及仅注射减毒活流感疫苗或安慰剂后第10天收集事件。结果:在1245名(99.5%)的可评估儿童中,麻疹,腮腺炎,风疹疫苗和水痘疫苗的血清反应率和几何平均滴度与活减毒流感疫苗或安慰剂的同时给药相似(麻疹的血清反应率为>或= 96% -腮腺炎-风疹疫苗,两组的水痘疫苗均≥82%)。单独减毒后,活减毒流感病毒疫苗中抑制血凝素的抗体的几何平均滴度和血清转化率相似(H3,B和H1菌株的血清转化率分别为98%,92%和44%) )或麻疹,腮腺炎,风疹和水痘疫苗(血清转化率分别为98%,96%和43%)。治疗组之间的反应原性事件和不良事件的发生率相似。结论:减毒活流感疫苗与麻疹,腮腺炎,风疹疫苗和水痘疫苗同时给药与单独给药相比具有相同的免疫原性,并且耐受性良好。

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