A Narrative Review of Pneumococcal Conjugate Vaccine Choices for Greater Access and Protection against Pneumococcal Diseases in the Philippines.

Q4 Medicine
Acta Medica Philippina Pub Date : 2025-03-31 eCollection Date: 2025-01-01 DOI:10.47895/amp.v59i4.10372
Maria Margarita M Lota, Rosario Z Capeding, Fernando B Garcia, John Robert C Medina, Jeremiah A Serrano, Carlo R Lumangaya, Vicente Y Belizario
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Abstract

Background: Pneumococcal vaccination has been widely used for the prevention of pneumococcal disease, with two types of vaccines available since 2009. With the World Health Organization (WHO) recommendation of incorporating pneumococcal conjugate vaccines (PCVs) in National Immunization Programs (NIPs) worldwide, a ten-valent PCV (PHiD-CV) was initially introduced in the Philippines in 2012. This, however, transitioned to the use of the 13-valent PCV (Prevnar) subsequent to the recommendation of the Formulary Executive Council in 2014.

Objective: This review aimed to present evidence on pneumococcal disease and vaccine inclusion in the Philippine NIP from 2005 - 2021.

Methods: This narrative review compiled articles on Pneumococcus from January 2005 to October 2021, sourcing literature from databases such as BIOSIS Preview, CAB Direct, Embase, Google Scholar, and others.

Results: In the Philippines, there was a shift in prevalent serotypes of Streptococcus pneumoniae among children under five following the introduction of PCV13 in the National Immunization Program in 2014, with serotype 14 becoming the most common by 2018, and a significant reduction in isolates reported in 2020, where only serotypes 5, 19A, and 23F were identified among invasive strains. The immunogenicity results of a potential vaccine candidate should be factored into the overall evidence when conducting a reassessment of PCV.

Conclusion: As part of the decision making about the inclusion of the PCVs in the NIP of the Philippines, various factors such as local epidemiology, vaccine supply, cost, and programmatic characteristics must be careful weighed. Enhancing laboratory and surveillance capacity are essential to provide evidence-based decision-making in terms of existing serotype distribution and antimicrobial resistance (AMR) profile in the country. With the introduction of a new affordable formulation of a 10-valent PCV offering a comparable serotype coverage, the reassessment of choice of PCV with the consideration of all three formulations, namely PCV13, PHiD-CV, and SIIPL-PCV, may be warranted.

菲律宾肺炎球菌结合疫苗选择的叙述性回顾,以提高肺炎球菌疾病的可及性和保护。
背景:肺炎球菌疫苗接种已被广泛用于预防肺炎球菌疾病,自2009年以来有两种类型的疫苗可用。根据世界卫生组织(WHO)关于将肺炎球菌结合疫苗(PCV)纳入全球国家免疫规划(NIPs)的建议,菲律宾于2012年首次引入了十价PCV (phids - cv)。然而,在2014年配方执行理事会提出建议后,这一做法转变为使用13价PCV (Prevnar)。目的:本综述旨在提供2005 - 2021年菲律宾国家免疫计划中肺炎球菌疾病和疫苗纳入的证据。方法:本叙述性综述汇编了2005年1月至2021年10月期间关于肺炎球菌的文章,文献来源包括BIOSIS Preview、CAB Direct、Embase、谷歌Scholar等数据库。结果:在菲律宾,2014年在国家免疫规划中引入PCV13后,五岁以下儿童中流行的肺炎链球菌血清型发生了变化,到2018年,血清型14成为最常见的,2020年报告的分离株显著减少,在入侵菌株中仅鉴定出血清型5、19A和23F。在对PCV进行重新评估时,应将潜在候选疫苗的免疫原性结果纳入总体证据。结论:在决定将pcv纳入菲律宾国家免疫规划时,必须仔细权衡当地流行病学、疫苗供应、成本和规划特点等各种因素。加强实验室和监测能力对于就该国现有血清型分布和抗菌素耐药性(AMR)情况提供基于证据的决策至关重要。随着可负担得起的10价PCV新制剂的推出,提供相当的血清型覆盖率,可能有必要重新评估PCV的选择,同时考虑所有三种制剂,即PCV13、PHiD-CV和SIIPL-PCV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta Medica Philippina
Acta Medica Philippina Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
199
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