Levels of SARS-CoV-2 population exposure are considerably higher than suggested by seroprevalence surveys.
Levels of SARS-CoV-2 population exposure are considerably higher than suggested by seroprevalence surveys.
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DOI:
10.1371/journal.pcbi.1009436
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发表时间:
2021-09
影响因子:
4.3
通讯作者:
Aguas R
中科院分区:
文献类型:
--
作者:
Chen S;Flegg JA;White LJ;Aguas R
Accurate knowledge of prior population exposure has critical ramifications for preparedness plans for future SARS-CoV-2 epidemic waves and vaccine prioritization strategies. Serological studies can be used to estimate levels of past exposure and thus position populations in their epidemic timeline. To circumvent biases introduced by the decay in antibody titers over time, methods for estimating population exposure should account for seroreversion, to reflect that changes in seroprevalence measures over time are the net effect of increases due to recent transmission and decreases due to antibody waning. Here, we present a new method that combines multiple datasets (serology, mortality, and virus positivity ratios) to estimate seroreversion time and infection fatality ratios (IFR) and simultaneously infer population exposure levels. The results indicate that the average time to seroreversion is around six months, IFR is 0.54% to 1.3%, and true exposure may be more than double the current seroprevalence levels reported for several regions of England. It is particularly challenging to determine the true proportion of the population that has been previously exposed to SARS-CoV-2. Serological surveys that measure how many people have antibodies against the virus are a promising tool but results from such studies need to be interpreted carefully. Several studies following individuals over time after they’ve had a known infection were able to determine that antibodies are only measurable up to 6–9 months, on average. The immediate implication is that serological studies will inevitably under-estimate the number of people exposed, since some will have a lower antibody count when the study is conducted and test negative. We propose a method that takes this into account and informs the true level of exposure from triangulating serological data with mortality and test positivity data.
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DOI:
10.1093/cid/ciab172
发表时间:
2021-12-16
期刊:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
影响因子:
--
作者:
den Hartog G;Vos ERA;van den Hoogen LL;van Boven M;Schepp RM;Smits G;van Vliet J;Woudstra L;Wijmenga-Monsuur AJ;van Hagen CCE;Sanders EAM;de Melker HE;van der Klis FRM;van Binnendijk RS
通讯作者:
van Binnendijk RS
DOI:
10.1016/s1473-3099(20)30943-9
发表时间:
2021-03
期刊:
The Lancet. Infectious diseases
影响因子:
--
作者:
Duysburgh E;Mortgat L;Barbezange C;Dierick K;Fischer N;Heyndrickx L;Hutse V;Thomas I;Van Gucht S;Vuylsteke B;Ariën KK;Desombere I
通讯作者:
Desombere I
影响因子:
82.9
作者:
Long, Quan-Xin;Liu, Bai-Zhong;Huang, Ai-Long
通讯作者:
Huang, Ai-Long
DOI:
10.1016/j.ijid.2020.09.1464
发表时间:
2020-12
期刊:
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases
影响因子:
--
作者:
Meyerowitz-Katz G;Merone L
通讯作者:
Merone L
DOI:
10.1016/s2666-5247(21)00025-2
发表时间:
2021-06
期刊:
The Lancet. Microbe
影响因子:
--
作者:
Chia WN;Zhu F;Ong SWX;Young BE;Fong SW;Le Bert N;Tan CW;Tiu C;Zhang J;Tan SY;Pada S;Chan YH;Tham CYL;Kunasegaran K;Chen MI;Low JGH;Leo YS;Renia L;Bertoletti A;Ng LFP;Lye DC;Wang LF
通讯作者:
Wang LF