Antigenicity and reactogenicity of influenza A/USSR/77 virus vaccine in children--a multicentered evaluation of dosage and safety.
Antigenicity and reactogenicity of influenza A/USSR/77 virus vaccine in children--a multicentered evaluation of dosage and safety.
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儿童甲型/苏联/77 流感病毒疫苗的抗原性和反应原性——剂量和安全性的多中心评价。
DOI:
10.1093/clinids/5.4.758
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发表时间:
1983
期刊:
影响因子:
--
通讯作者:
Taber,LH
中科院分区:
文献类型:
--
作者:
Wright,PF;Cherry,JD;Foy,HM;Glezen,WP;Hall,CB;McIntosh,K;Monto,AS;Parrott,RH;Portnoy,B;Taber,LH
Clinical trials of monovalent A/USSR/77 (H1N1) and trivalent A/USSR/77 (H1N1), A/Texas/77 (H3N2), and B/Hong Kong/72 inactivated influenza virus vaccines were carried out in 358children and adolescents. Only split-virus vaccines were administered to children younger than 13 years of age. No serious local or systemic reactions were observed among the study participants. Two doses of vaccine containing 7–20 µg of the A/USSR/77 (H1N1) viral antigen were required to achieve serum titers of hemagglutinin-inhibiting (HAI) antibody >1:40. However, single doses containing 7–20 µg of the A/Texas/77 (H3N2) or B/Hong Kong/72 antigens stimulated serum HAI antibody levels of 1:40.