Seroepidemiologic Study Designs for Determining SARS-COV-2 Transmission and Immunity
Hannah Clapham
, James Hay
1, Isobel Routledge
1, Saki Takahashi
1, Marc Choisy
2, Derek Cummings
2, Bryan Grenfell
2, C. Jessica E. Metcalf
2, Michael Mina
2, Isabel Rodriguez Barraquer
2, Henrik Salje
2, and Clarence C. Tam
2
Author affiliations: National University of Singapore Saw Swee Hock School of Public Health, Singapore (H. Clapham, C.C. Tam); Harvard University T.H. Chan School of Public Health, Boston, Massachusetts, USA (J. Hay, M. Mina); University of California San Francisco EPPIcenter Program, San Francisco, California, USA (I. Routledge, S. Takahashi, I. Rodriguez-Barraquer); University of California San Francisco Department of Medicine, San Francisco (I. Routledge, S. Takahashi, I. Rodriguez-Barraquer); Oxford University Clinical Research Unit–Vietnam, Ho Chi Minh City, Vietnam (M. Choisy); University of Florida Department of Biology, Gainesville, Florida, USA (D. Cummings); Princeton University, Princeton, New Jersey, USA (C.J.E. Metcalf, B. Grenfell); University of Cambridge, Cambridge, UK (H. Salje); London School of Hygiene and Tropical Medicine (C.C. Tam)
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Figure 2
Figure 2. Link between severe acute respiratory syndrome coronavirus 2 infection dynamics and serologic analysis designs. A) Example of results from cross-sectional population study design, indicating percentage of study population who are seropositive at each sample time point. B) Example of results from a cohort study design: percentage of study population who are seropositive at each sample time point. The difference in the study designs is shown in panels C and D. C) In a cross-sectional design, we only know proportions in the population; however, panel D shows an example of each person’s antibody titers over time, illustrating that in a cohort study we can follow the dynamics of antibody response over time (e.g., the proportion who seroconvert and person-to-person variability).
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Page created: June 02, 2020
Page updated: August 18, 2020
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