National Institute for Communicable Diseases, a Division of the National Health Laboratory Service, Johannesburg, South Africa.
Vaccine. 2012 Sep 7;30 Suppl 3:C21-7. doi: 10.1016/j.vaccine.2012.05.055.
In April 2009, South Africa was the first African country to introduce pneumococcal polysaccharide-protein conjugate vaccine (PCV) into its public immunization program. This review summarizes studies on pneumococcal epidemiology and PCV undertaken in South Africa, which contributed to the process of advocating for the inclusion of PCV into the public immunization program. Surveillance prior to the introduction of 7-valent PCV (PCV-7) indicated that 70% (418/593) of invasive pneumococcal disease (IPD) in infants, the age-group at highest risk of IPD, was attributable to PCV-7 serotypes. Furthermore, 65% of all IPD in children under-5 years was associated with underlying HIV infection. Initial immunogenicity studies reported that PCV vaccination of antiretroviral-naïve HIV-infected children was associated with lower geometric mean antibody concentrations and proportion with a serotype-specific antibody concentration above the putative threshold (≥0.35 μg/ml) of protection for IPD for some of the serotypes. The functionality of antibody induced by PCV in HIV-infected infants was inferior to that of HIV-uninfected infants. Vaccine efficacy of 9-valent PCV in a trial from South Africa reported an 83% reduction of vaccine-serotype IPD in HIV-uninfected children in the first two years of life, with protection persisting thereafter. However, vaccine efficacy against vaccine-serotype IPD declined from 65% at 2.3 years of age to 39% by six years of age in antiretroviral-naïve HIV-infected children. Based on the observation that a two-dose primary series of PCV during infancy resulted in similar immunogenicity compared to a three-dose schedule, as well as similar impact on nasopharyngeal colonization and effectiveness against IPD in HIV-uninfected children, the South African immunization program adopted a two-dose primary series with a booster dose at 9 months of age. This schedule was largely premised on containing the cost of vaccine introduction, whilst including a booster dose of PCV to assist in prolonging the duration of protection in HIV-infected children.
2009 年 4 月,南非成为首个将肺炎球菌多糖蛋白结合疫苗(PCV)纳入其公共免疫计划的非洲国家。本综述总结了南非开展的肺炎球菌流行病学和 PCV 研究,这些研究为倡导将 PCV 纳入公共免疫计划提供了依据。在引入 7 价 PCV(PCV-7)之前的监测表明,593 例侵袭性肺炎球菌病(IPD)患儿中有 70%(418/593)的发病归因于 PCV-7 血清型。此外,5 岁以下儿童所有 IPD 的 65%与潜在的 HIV 感染有关。初步免疫原性研究报告称,在未接受抗逆转录病毒治疗的 HIV 感染儿童中接种 PCV 疫苗与某些血清型的几何平均抗体浓度和具有特定血清型抗体浓度高于假定保护 IPD 阈值(≥0.35μg/ml)的比例较低有关。HIV 感染婴儿中 PCV 诱导的抗体功能不如 HIV 未感染婴儿。南非一项试验报告称,9 价 PCV 的疫苗效力可使 HIV 未感染儿童在生命的前两年中,疫苗血清型 IPD 减少 83%,此后仍保持保护作用。然而,在未接受抗逆转录病毒治疗的 HIV 感染儿童中,疫苗对疫苗血清型 IPD 的效力从 2.3 岁时的 65%下降至 6 岁时的 39%。基于在婴儿期接种两剂 PCV 基础免疫可产生与三剂方案相似的免疫原性,以及对鼻咽定植和 HIV 未感染儿童 IPD 有效性的相似影响的观察结果,南非免疫计划采用了两剂基础免疫,9 个月时加强一剂。该方案主要基于控制疫苗引入的成本,同时加强一剂 PCV 以帮助延长 HIV 感染儿童的保护持续时间。