Pneumococcal Laboratory, Murdoch Childrens Research Institute, Melbourne, Australia.
J Allergy Clin Immunol. 2012 Mar;129(3):794-800.e2. doi: 10.1016/j.jaci.2011.11.043. Epub 2012 Feb 2.
Infections with Streptococcus pneumoniae (pneumococcus) are a cause of significant child mortality. Pneumococcal glycoconjugate vaccines are expensive and provide limited serotype coverage. The 23-valent pneumococcal polysaccharide vaccine (Pneumovax) might provide wider serotype coverage but is reported to be weakly immunogenic in children less than 2 years of age. We have previously reported that Pneumovax administered to healthy 12-month-old Fijian infants elicits significant serotype-specific IgG responses. However, the functional capacity of these responses in 12-month-old infants is not known.
We sought to assess the functional, serotype-specific immune response of 12-month-old infants after immunization with Pneumovax.
Functional responses of 12-month-old infants were assessed by using the opsonophagocytic and antibody avidity assay against 8 serotypes and 23 serotypes, respectively.
Seventy-one percent of infants produced strong opsonophagocytic activity against 4 of 8 serotypes, and 30% produced high-avidity serotype-specific IgG antibodies to 10 of 23 serotypes at 2 weeks after Pneumovax. Responses were protective for most serotypes that cause disease in Western countries, whereas responses to most of the epidemiologically relevant serotypes for developing countries were low.
This is the first comprehensive study evaluating the functional antibody response to Pneumovax in 12-month-old infants. Pneumovax induced functional antibody responses to several serotypes causing disease in Western countries but induced poorer responses to serotypes that are responsible for the majority of disease in developing countries. Pneumovax might be of benefit in some populations, but further studies are required before this can be recommended in developing countries.
肺炎链球菌(肺炎球菌)感染是导致儿童死亡的重要原因。肺炎球菌结合疫苗价格昂贵,且只能提供有限的血清型覆盖范围。23 价肺炎球菌多糖疫苗(Pneumovax)可能提供更广泛的血清型覆盖范围,但据报道,在 2 岁以下儿童中的免疫原性较弱。我们之前报道过,在健康的 12 个月大的斐济婴儿中接种 Pneumovax 可引起显著的血清型特异性 IgG 反应。然而,这些反应在 12 个月大的婴儿中的功能能力尚不清楚。
我们旨在评估 12 个月大婴儿接种 Pneumovax 后的功能、血清型特异性免疫反应。
使用针对 8 种血清型和 23 种血清型的调理吞噬和抗体亲和性测定法评估 12 个月大婴儿的功能反应。
71%的婴儿在接种 Pneumovax 后 2 周内对 4 种 8 种血清型中的 4 种产生了强烈的调理吞噬活性,30%对 23 种血清型中的 10 种产生了高亲和力的血清型特异性 IgG 抗体。对于大多数导致西方国家疾病的血清型,反应具有保护作用,而对于发展中国家与流行病学相关的大多数血清型,反应较低。
这是第一项全面评估 12 个月大婴儿接种 Pneumovax 后功能抗体反应的研究。Pneumovax 诱导了对几种导致西方国家疾病的血清型的功能性抗体反应,但对导致发展中国家大多数疾病的血清型的反应较差。Pneumovax 在某些人群中可能有益,但在发展中国家推荐使用之前,还需要进一步研究。