Wuorimaa T, Dagan R, Väkeväinen M, Bailleux F, Haikala R, Yaich M, Eskola J, Käyhty H
Department of Vaccines, Vaccine Immunology Laboratory, National Public Health Institute, Mannerheimintie 166, 00300 Helsinki, Finland.
J Infect Dis. 2001 Nov 1;184(9):1211-5. doi: 10.1086/323648. Epub 2001 Sep 25.
Finnish and Israeli infants received an 11-valent mixed-carrier pneumococcal conjugate vaccine with or without aluminum adjuvant at 2, 4, 6, and 12 months of age. The relative avidity of serotype 1-, 5-, 6B-, 14-, 19F-, and 23F-specific IgG antibodies in serum obtained at 7, 12, and 13 months of age was measured by EIA, using thiocyanate as a chaotropic agent. For all serotypes, except 14, avidity increased between the ages of 7 and 12 months. After boosting at 12 months, avidity further increased for all serotypes. The adjuvant improved antibody avidity against serotype 5. The IgG antibodies produced were mainly IgG1 subclass, although some infants also produced IgG2 after boosting. In conclusion, the immunization of infants with this 11-valent pneumococcal conjugate vaccine increased avidity of IgG, suggesting successful immunologic priming.
芬兰和以色列的婴儿在2、4、6和12月龄时接种了含或不含铝佐剂的11价混合载体肺炎球菌结合疫苗。在7、12和13月龄时采集血清,采用硫氰酸盐作为离液剂,通过酶免疫测定法(EIA)检测血清中1、5、6B、14、19F和23F型特异性IgG抗体的相对亲和力。除14型外,所有血清型的亲和力在7至12月龄之间均有所增加。在12月龄加强免疫后,所有血清型的亲和力进一步增加。佐剂提高了针对5型血清型的抗体亲和力。产生的IgG抗体主要为IgG1亚类,不过一些婴儿在加强免疫后也产生了IgG2。总之,用这种11价肺炎球菌结合疫苗对婴儿进行免疫接种可提高IgG的亲和力,表明免疫启动成功。