Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
MRC Tropical Epidemiology Group, London School of Hygiene & Tropical Medicine, London, UK.
Vaccine. 2019 Nov 28;37(50):7381-7390. doi: 10.1016/j.vaccine.2017.10.011. Epub 2018 Jan 17.
According to the 2015 Global Burden of Disease Study, diarrhea ranked ninth among causes of death for all ages, and fourth among children under 5 years old, accounting for an estimated 499,000 deaths in this young age group. It was also the second most common cause of years lived with disability (2.39 billion YLDs). The goal of the WHO/UNICEF Integrated Global Action Plan for the Prevention and Control of Pneumonia and Diarrhea (GAPPD) is to reduce deaths from diarrhea in children under 5 years of age to less than 1 per 1000 live births, by 2025. Development of new and improved vaccines against diarrheal infections is a fundamental element of the strategy towards achieving this goal. Enterotoxigenic Escherichia coli (ETEC) and Shigella are enteropathogens that cause significant global mortality and morbidity, particularly in low- and middle-income countries. In 2016, WHO's Product Development for Vaccines Advisory Committee (PDVAC) recommended that the WHO's Initiative for Vaccine Research (IVR) engage in this area, based on PDVAC's criteria of prioritizing the development of vaccines against pathogens that will address a major unmet public health need, and for which clinical candidates with a good probability of technical success are in the pipeline. As a first step, WHO's IVR convened global subject matter experts to discuss the current global ETEC and Shigella disease burden estimates, including the current understanding of the long-term indirect effects of ETEC and Shigella infection, and how these data may affect future decision making on vaccine development for both pathogens. The available global burden estimates for ETEC and Shigella differ with respect to the relative importance of these two pathogens. The mortality estimates vary between iterations published by the same group, as well as between estimates of different groups, although the uncertainty intervals are broad and overlapping. These variances are attributable to differences in the data available and incorporated in the models; the methods used to detect the pathogens; the modelling methodologies; and, to actual changes in the total number of diarrheal deaths over time. The changes in the most recently reported mortality estimates for these pathogens, as compared to previous iterations, has led to debate as to whether investment in development of stand-alone vaccines, rather than combined vaccines, is warranted from cost-effectiveness and vaccine impact perspectives. Further work will be needed to understand better the variances and uncertainties in the reported mortality estimates to support investment decision making, and ultimately policy recommendations for vaccine use. In addition, a comprehensive assessment of the value proposition for vaccines against these pathogens is needed and will be strengthened if the long-term health consequences associated with diarrhea and dysentery due to these pathogens are better defined.
根据 2015 年全球疾病负担研究,腹泻在所有年龄段的死因中排名第九,在 5 岁以下儿童中排名第四,估计在这个年轻年龄段有 49.9 万人死亡。它也是导致伤残调整生命年(DALYs)的第二大常见原因(23.9 亿 DALYs)。世卫组织/儿基会预防和控制肺炎和腹泻综合全球行动计划(GAPPD)的目标是将 5 岁以下儿童因腹泻导致的死亡减少到每 1000 例活产少于 1 例,到 2025 年实现这一目标。开发针对腹泻感染的新的和改进的疫苗是实现这一目标战略的一个基本要素。肠致病性大肠杆菌(ETEC)和志贺氏菌是引起全球死亡率和发病率的病原体,特别是在低收入和中等收入国家。2016 年,世卫组织疫苗研发咨询委员会(PDVAC)根据 PDVAC 的标准,即优先考虑开发针对将解决重大未满足公共卫生需求的病原体的疫苗,以及有良好技术成功可能性的临床候选疫苗正在进行中,建议世卫组织疫苗研发倡议(IVR)参与这一领域。作为第一步,世卫组织 IVR 召集了全球专题专家,讨论当前 ETEC 和志贺氏菌疾病全球负担的估计情况,包括对 ETEC 和志贺氏菌感染长期间接影响的当前认识,以及这些数据如何影响未来对这两种病原体疫苗开发的决策。ETEC 和志贺氏菌的可用全球负担估计数因这两种病原体的相对重要性而有所不同。同一组发布的迭代版本之间以及不同组的估计数之间的死亡率估计数各不相同,尽管不确定性区间很宽且相互重叠。这些差异归因于模型中包含的不同数据;用于检测病原体的方法;建模方法;以及随着时间的推移,腹泻总死亡人数的实际变化。与前几次迭代相比,这些病原体最近报告的死亡率估计数的变化引发了关于是否有理由从成本效益和疫苗效果的角度投资开发单独疫苗而不是联合疫苗的争论。需要进一步开展工作,以更好地了解报告的死亡率估计数中的差异和不确定性,以支持投资决策,并最终为疫苗使用提供政策建议。此外,如果能更好地确定与这些病原体相关的腹泻和痢疾的长期健康后果,就需要对这些病原体疫苗的价值主张进行全面评估,这一评估将得到加强。