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通过对免疫未接触人群的血清学和临床监测推断未检测到的霍乱感染比例。

Inferring the proportion of undetected cholera infections from serological and clinical surveillance in an immunologically naive population.

作者信息

Finger Flavio, Lemaitre Joseph, Juin Stanley, Jackson Brendan, Funk Sebastian, Lessler Justin, Mintz Eric, Dely Patrick, Boncy Jacques, Azman Andrew S

机构信息

Centre for the Mathematical Modelling of Infectious Diseases, London School of Hygiene and Tropical Medicine, London, UK.

Epicentre, Paris, France.

出版信息

Epidemiol Infect. 2024 Dec 2;152:e149. doi: 10.1017/S0950268824000888.

DOI:10.1017/S0950268824000888
PMID:39618115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11626459/
Abstract

Most infections with pandemic are thought to result in subclinical disease and are not captured by surveillance. Previous estimates of the ratio of infections to clinical cases have varied widely (2 to 100 infections per case). Understanding cholera epidemiology and immunity relies on the ability to translate between numbers of clinical cases and the underlying number of infections in the population. We estimated the infection incidence during the first months of an outbreak in a cholera-naive population using a Bayesian vibriocidal antibody titer decay model combining measurements from a representative serosurvey and clinical surveillance data. 3,880 suspected cases were reported in Grande Saline, Haiti, between 20 October 2010 and 6 April 2011 (clinical attack rate 18.4%). We found that more than 52.6% (95% Credible Interval (CrI) 49.4-55.7) of the population ≥2 years showed serologic evidence of infection, with a lower infection rate among children aged 2-4 years (35.5%; 95%CrI 24.2-51.6) compared with people ≥5 years (53.1%; 95%CrI 49.4-56.4). This estimated infection rate, nearly three times the clinical attack rate, with underdetection mainly seen in those ≥5 years, has likely impacted subsequent outbreak dynamics. Our findings show how seroincidence estimates improve understanding of links between cholera burden, transmission dynamics and immunity.

摘要

大多数甲型流感感染被认为会导致亚临床疾病,并且未被监测到。先前对感染与临床病例比例的估计差异很大(每例临床病例有2至100次感染)。了解霍乱流行病学和免疫力依赖于在临床病例数与人群中潜在感染数之间进行转换的能力。我们使用贝叶斯杀弧菌抗体滴度衰减模型,结合代表性血清学调查和临床监测数据的测量结果,估计了霍乱易感人群中疫情爆发头几个月的感染发病率。2010年10月20日至2011年4月6日期间,海地大萨利纳报告了3880例疑似病例(临床发病率18.4%)。我们发现,≥2岁人群中超过52.6%(95%可信区间(CrI)49.4 - 55.7)有感染的血清学证据,2 - 4岁儿童的感染率(35.5%;95%CrI 24.2 - 51.6)低于≥5岁人群(53.1%;95%CrI 49.4 - 56.4)。这一估计的感染率几乎是临床发病率的三倍,漏检主要见于≥5岁人群,这可能影响了随后的疫情动态。我们的研究结果表明血清发病率估计如何有助于更好地理解霍乱负担、传播动态和免疫力之间的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/adf41948c820/S0950268824000888_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/062cc933aa8c/S0950268824000888_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/8f371ffefc52/S0950268824000888_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/adf41948c820/S0950268824000888_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/062cc933aa8c/S0950268824000888_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/8f371ffefc52/S0950268824000888_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3437/11626459/adf41948c820/S0950268824000888_fig3.jpg

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