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使用减毒活冷适应重组甲型H1N1、H3N2流感病毒及乙型流感病毒疫苗对福利院哮喘儿童和精神运动发育迟缓患者进行免疫接种。

Immunization of institutionalized asthmatic children and patients with psychomotor retardation using live attenuated cold-adapted reassortment influenza A H1N1, H3N2 and B vaccines.

作者信息

Miyazaki C, Nakayama M, Tanaka Y, Kusuhara K, Okada K, Tokugawa K, Ueda K, Shibata R, Nishima S, Yamane N

机构信息

Department of Pediatrics, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Vaccine. 1993;11(8):853-8. doi: 10.1016/0264-410x(93)90361-z.

Abstract

Live attenuated cold-adapted reassortant (CR) influenza virus vaccines were evaluated in institutionalized asthmatic children and severe psychomotor-retarded (SPR) patients. Almost all the vaccinees were seropositive to the vaccine strains before immunization. Trivalent CR vaccine (containing A H1N1 (CR-125), A H3N2 (CR-149) and B (CRB-117)), bivalent CR vaccine (CR-125 and CR-149) and monovalent CRB-117 were inoculated to 19 asthmatic children and 36 and 16 SPR patients, respectively. Overall 49, 22, and 11% of vaccinees were infected by A H1N1, A H3N2 or B vaccine viruses, respectively, as indicated by significant haemagglutination-inhibition (HI) antibody titre rises 4 weeks after inoculation. No severe adverse reactions associated with CR vaccination were observed in the handicapped patients. A nosocomial outbreak of influenza A H1N1 occurred in the ward with asthmatic children, but none of the 19 CR-trivalent vaccinees became infected. However, five of 20 non-vaccinees in the same ward, and ten of 30 vaccinees in another ward that received inactivated split vaccine became infected. The CR vaccines demonstrated significant protective effects against natural exposure to the A H1N1 virus, and were well tolerated and safe when given to patients with bronchial asthma and severe psychomotor retardation.

摘要

对减毒活冷适应重配(CR)流感病毒疫苗在机构化哮喘儿童和严重精神运动发育迟缓(SPR)患者中进行了评估。几乎所有接种者在免疫前对疫苗毒株血清呈阳性。将三价CR疫苗(含A H1N1(CR - 125)、A H3N2(CR - 149)和B(CRB - 117))、二价CR疫苗(CR - 125和CR - 149)和单价CRB - 117分别接种给19名哮喘儿童以及36名和16名SPR患者。接种后4周,血凝抑制(HI)抗体效价显著升高,表明总体分别有49%、22%和11%的接种者被A H1N1、A H3N2或B疫苗病毒感染。在残疾患者中未观察到与CR疫苗接种相关的严重不良反应。在有哮喘儿童的病房发生了A H1N1流感的医院内暴发,但19名接种三价CR疫苗的儿童均未感染。然而,同一病房的20名未接种者中有5人感染,另一个接种灭活裂解疫苗的病房的30名接种者中有10人感染。CR疫苗对自然接触A H1N1病毒显示出显著的保护作用,并且在给予支气管哮喘和严重精神运动发育迟缓患者时耐受性良好且安全。

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