A Mixture Model for Estimating SARS-CoV-2 Seroprevalence in Chennai, India.

A Mixture Model for Estimating SARS-CoV-2 Seroprevalence in Chennai, India.
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DOI:
10.1093/aje/kwad103
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发表时间:
2023-09-01
影响因子:
5
通讯作者:
Solomon SS
Solomon SS
中科院分区:
医学2区
文献类型:
--
作者:
Hitchings MDT;Patel EU;Khan R;Srikrishnan AK;Anderson M;Kumar KS;Wesolowski AP;Iqbal SH;Rodgers MA;Mehta SH;Cloherty G;Cummings DAT;Solomon SS

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用于估计严重急性呼吸道综合征冠状病毒2(SARS-CoV-2)流行率的血清学检测通常依赖于制造商根据严重病例确定的临界值。我们于2021年1月至5月在印度钦奈对4,677名个体进行了基于家庭的血清调查。对样本进行了针对刺突蛋白(S)和核衣壳蛋白(N)的SARS-CoV-2免疫球蛋白G(IgG)抗体检测。我们计算血清阳性率,使用制造商临界值和基于测量的IgG水平的混合模型定义血清阳性。使用生产商临界值,每种检测方法估计的血清阳性率存在5倍差异。使用混合物模型在很大程度上调和了这种差异,估计的抗S和抗N IgG血清阳性率分别为64.9%(95%可信区间(CrI):63.8,66.0)和51.5%(95%CrI:50.2,52.9)。年龄和社会经济因素显示不一致的关系与抗S和抗N IgG血清阳性使用制造商截止。在混合模型中,年龄与血清阳性无关,改善家庭通风与较低的血清阳性几率相关。随着全球疫苗规模的扩大,由于在几种疫苗中包含S蛋白,更稳定的抗S IgG检测的实用性可能受到限制。使用替代靶标估计SARS-CoV-2血清阳性率必须考虑血清反应的异质性,以确保血清阳性率不会被低估,相关性不会被误解。
Serological assays used to estimate the prevalence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) often rely on manufacturers’ cutoffs established on the basis of severe cases. We conducted a household-based serosurvey of 4,677 individuals in Chennai, India, from January to May 2021. Samples were tested for SARS-CoV-2 immunoglobulin G (IgG) antibodies to the spike (S) and nucleocapsid (N) proteins. We calculated seroprevalence, defining seropositivity using manufacturer cutoffs and using a mixture model based on measured IgG level. Using manufacturer cutoffs, there was a 5-fold difference in seroprevalence estimated by each assay. This difference was largely reconciled using the mixture model, with estimated anti-S and anti-N IgG seroprevalence of 64.9% (95% credible interval (CrI): 63.8, 66.0) and 51.5% (95% CrI: 50.2, 52.9), respectively. Age and socioeconomic factors showed inconsistent relationships with anti-S and anti-N IgG seropositivity using manufacturer cutoffs. In the mixture model, age was not associated with seropositivity, and improved household ventilation was associated with lower seropositivity odds. With global vaccine scale-up, the utility of the more stable anti-S IgG assay may be limited due to the inclusion of the S protein in several vaccines. Estimates of SARS-CoV-2 seroprevalence using alternative targets must consider heterogeneity in seroresponse to ensure that seroprevalence is not underestimated and correlates are not misinterpreted.
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