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RIX4414 减毒活人类轮状病毒疫苗在成人、幼儿及既往未感染婴儿中的安全性和免疫原性。

Safety and immunogenicity of RIX4414 live attenuated human rotavirus vaccine in adults, toddlers and previously uninfected infants.

作者信息

Vesikari T, Karvonen A, Korhonen T, Espo M, Lebacq E, Forster J, Zepp F, Delem A, De Vos B

机构信息

Medical School/FM3, University of Tampere, 33014, Finland.

出版信息

Vaccine. 2004 Jul 29;22(21-22):2836-42. doi: 10.1016/j.vaccine.2004.01.044.

Abstract

A live attenuated human rotavirus (HRV) vaccine, strain RIX4414, was tested sequentially in adults, previously infected toddlers, and previously uninfected infants. A single dose was given to adults and toddlers and found well tolerated. Next, a dose ranging (three different viral concentrations) safety and immunogenicity study was conducted in rotavirus IgA antibody negative infants (N= 192), who received two doses of RIX4414 vaccine or placebo at 2 and 4 months of age. No side effects were seen after vaccination. Specifically, administration of RIX4414 vaccine was not temporally associated with fever, diarrhea, or increase in liver transaminases. Rotavirus IgA seroconversion ranged from 50 to 88% after one dose and from 73 to 96% after two doses, depending on vaccine titer. After the first dose, on days 7-9 post vaccination, between 38 and 60% of the infants shed the vaccine virus, whereas after the second dose only 0 to 13% of the vaccinees shed the vaccine virus. It is concluded that RIX4414 strain HRV vaccine is virtually non-reactogenic and, at high titer, highly immunogenic in susceptible infants.

摘要

一种减毒活人类轮状病毒(HRV)疫苗,RIX4414株,先后在成人、既往感染的幼儿和既往未感染的婴儿中进行了测试。给成人和幼儿接种了单剂疫苗,发现耐受性良好。接下来,在轮状病毒IgA抗体阴性的婴儿(N = 192)中进行了剂量范围(三种不同病毒浓度)的安全性和免疫原性研究,这些婴儿在2个月和4个月大时接受了两剂RIX4414疫苗或安慰剂。接种疫苗后未观察到副作用。具体而言,接种RIX4414疫苗与发热、腹泻或肝转氨酶升高没有时间上的关联。根据疫苗滴度,一剂后轮状病毒IgA血清转化率为50%至88%,两剂后为73%至96%。接种第一剂后,在接种后第7 - 9天,38%至60%的婴儿排出疫苗病毒,而接种第二剂后,只有0%至13%的接种者排出疫苗病毒。结论是,RIX4414株HRV疫苗实际上无反应原性,并且在高滴度时,对易感婴儿具有高度免疫原性。

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