Vesikari Timo, Karvonen Aino, Forrest Bruce D, Hoshino Yasutaka, Chanock Robert M, Kapikian Albert Z
University of Tampere Medical School, Biokatu 10, 33520 Tampere, Finland.
Pediatr Infect Dis J. 2006 Feb;25(2):118-22. doi: 10.1097/01.inf.0000199288.98370.71.
Administration of the first dose of rhesus rotavirus-based tetravalent (RRV-TV) vaccine is followed by a transient febrile reaction at 3-4 days postvaccination in about one-third of vaccinees. We hypothesized that giving the first dose of RRV-TV vaccine during the neonatal period might reduce the reactogenicity of RRV-TV vaccine without compromising the utilization of the vaccine.
A double blind placebo-controlled safety and immunogenicity trial of 90 infants who received RRV-TV vaccine at 0-4-6, 0-2-4 or 2-4-6 months of age was conducted. Reactions were evaluated for 1 week after each vaccination and, in addition, serum specimens were collected before vaccination and at 5 and 7 months of age.
Febrile reactions were not observed in 62 infants receiving the first dose of RRV-TV vaccine during the neonatal period. Five of the 28 (18%) infants receiving the first dose at 2 months were febrile on 1 or more days, whereas none of the 30 infants who had received a neonatal dose developed a fever when vaccinated again at 2 months of age. An enzyme-linked immunosorbent assay IgA antibody response after 3 doses was observed significantly less frequently (77%) in infants who had received a neonatal dose, a second dose at 2 months of age, and a third dose at 4 months of age compared with those who received their first dose at 2 months and a second dose at 4 months (100%, P < 0.02). Also, the frequency of a neutralizing antibody response to RRV and human rotavirus serotypes G1-4 tended to be lower in the group that had received the vaccine at 0-2-4 months compared with those who received it at 2-4-6 months. When the 2 tests were combined, the frequency of a seroresponse following the 0-2-4 month schedule (94%) was comparable with that following the 2-4-6 month schedule (100%).
Infants who received the first dose of RRV-TV vaccine during the neonatal period did not develop a febrile reaction. The immune response in a 3-dose schedule initiated in the neonatal period is somewhat dampened but still acceptable. Neonatal immunization might also reduce the very small risk of intussusception, which has been associated with administration of RRV-TV vaccine to older infants.
接种第一剂恒河猴轮状病毒四价疫苗(RRV-TV)后,约三分之一的接种者在接种后3 - 4天会出现短暂发热反应。我们推测在新生儿期接种第一剂RRV-TV疫苗可能会降低该疫苗的反应原性,同时不影响疫苗的效用。
对90名分别在0 - 4 - 6、0 - 2 - 4或2 - 4 - 6月龄接种RRV-TV疫苗的婴儿进行了一项双盲安慰剂对照安全性和免疫原性试验。每次接种后对反应进行1周评估,此外,在接种前以及5和7月龄时采集血清样本。
62名在新生儿期接种第一剂RRV-TV疫苗的婴儿未出现发热反应。28名在2月龄接种第一剂的婴儿中有5名(18%)在1天或多天出现发热,而30名接种过新生儿剂量疫苗的婴儿在2月龄再次接种时均未发热。与在2月龄接种第一剂、4月龄接种第二剂的婴儿相比,在新生儿期接种一剂、2月龄接种第二剂、4月龄接种第三剂的婴儿在3剂接种后酶联免疫吸附测定IgA抗体反应的发生率显著较低(77% 对100%,P < 0.02)。此外,与在2 - 4 - 6月龄接种疫苗的婴儿相比,在0 - 2 - 4月龄接种疫苗的婴儿中对RRV和人轮状病毒G1 - 4血清型的中和抗体反应频率也趋于较低。当将这两项检测结合起来时,0 - 2 - 4月龄接种方案后的血清反应频率(94%)与2 - 4 - 6月龄接种方案后的频率(100%)相当。
在新生儿期接种第一剂RRV-TV疫苗的婴儿未出现发热反应。在新生儿期开始的3剂接种方案中的免疫反应有所减弱,但仍可接受。新生儿免疫接种还可能降低与给较大婴儿接种RRV-TV疫苗相关的极微小肠套叠风险。