Gross P A, Ennis F A, Gaerlan P F, Denning C R, Setia U, Davis W J, Bisberg D S
J Clin Microbiol. 1981 Nov;14(5):534-8. doi: 10.1128/jcm.14.5.534-538.1981.
Split-product vaccines (SPVs) combine the desirable properties of no systemic reactogenicity and adequate immunogenicity when two doses are given. We compared a new Triton X-100 SPV (Connaught Laboratories, Inc.) with the commercially available Tween-ether SPV (Parke-Davis & Co.) in 76 children and young adults 2 to 25 years old; there were 39 and 37, respectively, in each vaccine group. Both vaccines contained influenza A/Brazil/78, A/Texas/77, and B/Hong Kong/72 (7 microgram of hemagglutinin for each strain); two doses were administered 1 month apart. Among persons seronegative by the hemagglutination inhibition test, the geometric mean antibody titers rose to approximately 100 after the first vaccination for influenza A/Brazil/78 and A/Texas/77. For B/Hong Kong/72, however, seronegative recipients developed lower geometric mean titers of approximately 32 after one immunization. Against the new B/Singapore/79 strain neither SPV stimulated adequate cross-reacting hemagglutination inhibition antibody (geometric mean titers of approximately 10). In conclusion, the new Triton X-100 SPV appears to be comparable to the ether-treated SPV in primed subjects. Further studies in unprimed children should be done to confirm this impression. In addition, it would be advisable to study other dosage regimens in unprimed children with these SPVs.
分裂产物疫苗(SPV)在接种两剂时兼具无全身反应原性和足够免疫原性的理想特性。我们将一种新型的吐温X - 100 SPV(康诺特实验室公司)与市售的吐温醚SPV(帕克 - 戴维斯公司)在76名2至25岁的儿童和年轻人中进行了比较;每个疫苗组分别有39人和37人。两种疫苗均含有甲型/巴西/78、甲型/得克萨斯/77和乙型/香港/72(每种毒株含7微克血凝素);两剂疫苗间隔1个月接种。在血凝抑制试验血清阴性的人群中,接种第一剂疫苗后,甲型/巴西/78和甲型/得克萨斯/77的几何平均抗体滴度升至约100。然而,对于乙型/香港/72,血清阴性的接种者在一次免疫后产生的几何平均滴度较低,约为32。针对新的乙型/新加坡/79毒株,两种SPV均未刺激产生足够的交叉反应血凝抑制抗体(几何平均滴度约为10)。总之,新型吐温X - 100 SPV在已接种疫苗的受试者中似乎与醚处理的SPV相当。应在未接种疫苗的儿童中进行进一步研究以证实这一结论。此外,对未接种疫苗的儿童使用这些SPV研究其他给药方案是可取的。