TY - JOUR
T1 - Seroprevalence of immunoglobulin G antibodies against SARS-CoV-2 in Cyprus
AU - Papaneophytou, Christos
AU - Nicolaou, Andria
AU - Pieri, Myrtani
AU - Nicolaidou, Vicky
AU - Galatou, Eleftheria
AU - Sarigiannis, Yiannis
AU - Pantelidou, Markella
AU - Panayi, Pavlos
AU - Thoma, Theklios
AU - Stavraki, Antonia
AU - Argyrou, Xenia
AU - Kalogiannis, Tasos
AU - Yiannoukas, Kyriacos
AU - Petrou, Christos C.
AU - Felekkis, Kyriacos
N1 - Funding Information:
The study was supported internally by the University of Nicosia and Yiannoukas Medical Laboratories/Bioiatriki Group. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors did not receive any salary from the funders as part of this work. We would like to express our special thanks to SIEMENS Healthcare which technical support throughout the study.
Publisher Copyright:
Copyright: © 2022 Papaneophytou et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
PY - 2022/6
Y1 - 2022/6
N2 - Monitoring the levels of IgG antibodies against the SARS-CoV-2 is important during the coronavirus disease 2019 (COVID-19) pandemic, to plan an adequate and evidence-based public health response. After this study we report that the plasma levels of IgG antibodies against SARS-CoV-2 spike protein were higher in individuals with evidence of prior infection who received at least one dose of either an mRNA-based vaccine (Comirnaty BNT162b2/Pfizer-BioNTech or Spikevax mRNA-1273/Moderna) or an adenoviral-based vaccine (Vaxzervia ChAdOx1 nCoV-19/Oxford-Astra Zeneca) (n = 39) compared to i) unvaccinated individuals with evidence of prior infection with SARS-CoV-2 (n = 109) and ii) individuals without evidence of prior infection with SARS-CoV-2 who received one or two doses of one of the aforementioned vaccines (n = 342). Our analysis also revealed that regardless of the vaccine technology (mRNA-based and adenoviral vector-based) two doses achieved high anti-SARS-CoV-2 IgG responses. Our results indicate that vaccine-induced responses lead to higher levels of IgG antibodies compared to those produced following infection with the virus. Additionally, in agreement with previous studies, our results suggest that among individuals previously infected with SARS-CoV-2, even a single dose of a vaccine is adequate to elicit high levels of antibody response.
AB - Monitoring the levels of IgG antibodies against the SARS-CoV-2 is important during the coronavirus disease 2019 (COVID-19) pandemic, to plan an adequate and evidence-based public health response. After this study we report that the plasma levels of IgG antibodies against SARS-CoV-2 spike protein were higher in individuals with evidence of prior infection who received at least one dose of either an mRNA-based vaccine (Comirnaty BNT162b2/Pfizer-BioNTech or Spikevax mRNA-1273/Moderna) or an adenoviral-based vaccine (Vaxzervia ChAdOx1 nCoV-19/Oxford-Astra Zeneca) (n = 39) compared to i) unvaccinated individuals with evidence of prior infection with SARS-CoV-2 (n = 109) and ii) individuals without evidence of prior infection with SARS-CoV-2 who received one or two doses of one of the aforementioned vaccines (n = 342). Our analysis also revealed that regardless of the vaccine technology (mRNA-based and adenoviral vector-based) two doses achieved high anti-SARS-CoV-2 IgG responses. Our results indicate that vaccine-induced responses lead to higher levels of IgG antibodies compared to those produced following infection with the virus. Additionally, in agreement with previous studies, our results suggest that among individuals previously infected with SARS-CoV-2, even a single dose of a vaccine is adequate to elicit high levels of antibody response.
UR - http://www.scopus.com/inward/record.url?scp=85131969205&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0269885
DO - 10.1371/journal.pone.0269885
M3 - Article
C2 - 35696396
AN - SCOPUS:85131969205
SN - 1932-6203
VL - 17
JO - PLoS ONE
JF - PLoS ONE
IS - 6 June
M1 - e0269885
ER -