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Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand

BACKGROUND: In Thailand, early vaccination initiatives for SARS-CoV-2 relied on CoronaVac (Sinovac Life Sciences) and ChAdOx1 (Oxford–AstraZeneca) vaccines. However, the data of immunogenicity of these two vaccines in Thai populations is limited. This real time, head-to-head comparative study was co...

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Autores principales: Hongjaisee, Sayamon, Chawansuntati, Kriangkrai, Sripan, Patumrat, Rattanathammethee, Kritsadee, Sakkhachornphop, Supachai, Chaiwarith, Romanee, Sudjaritruk, Tavitiya, Supparatpinyo, Khuanchai, Wipasa, Jiraprapa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119672/
https://www.ncbi.nlm.nih.gov/pubmed/37155476
http://dx.doi.org/10.1016/j.jvacx.2023.100305
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author Hongjaisee, Sayamon
Chawansuntati, Kriangkrai
Sripan, Patumrat
Rattanathammethee, Kritsadee
Sakkhachornphop, Supachai
Chaiwarith, Romanee
Sudjaritruk, Tavitiya
Supparatpinyo, Khuanchai
Wipasa, Jiraprapa
author_facet Hongjaisee, Sayamon
Chawansuntati, Kriangkrai
Sripan, Patumrat
Rattanathammethee, Kritsadee
Sakkhachornphop, Supachai
Chaiwarith, Romanee
Sudjaritruk, Tavitiya
Supparatpinyo, Khuanchai
Wipasa, Jiraprapa
author_sort Hongjaisee, Sayamon
collection PubMed
description BACKGROUND: In Thailand, early vaccination initiatives for SARS-CoV-2 relied on CoronaVac (Sinovac Life Sciences) and ChAdOx1 (Oxford–AstraZeneca) vaccines. However, the data of immunogenicity of these two vaccines in Thai populations is limited. This real time, head-to-head comparative study was conducted to investigate antibody (Ab) responses to SARS-CoV-2 following infection or receipt of either CoronaVac or ChAdOx1 vaccination in Chiang Mai, Thailand. METHODS: Sera was collected within two months from participants having a history of documented SARS-CoV-2 infection or at one month after the second dose of CoronaVac vaccine. Sera from participants with a history of receiving one dose of ChAdOx1 vaccination was collected twice, at one month following each vaccine dose. Neutralizing antibodies (NAbs) were assessed using the surrogate neutralization test and anti-spike protein antibodies were assessed using an in-house enzyme-linked immunosorbent assay. RESULTS: The prevalence of NAbs against SARS-CoV-2 was 92.1 %, 95.7 %, 64.1 % and 100 % in the infection group, CoronaVac group, ChAdOx1 group after 1st dose, and ChAdOx1 group after 2nd dose, respectively. The inhibition rate in individuals receiving two doses of ChAdOx1 vaccine (90.8%) was significantly higher than individuals who had recovered from natural infection (71.7%) or individuals who had received two doses of CoronaVac vaccine (66.7%). The prevalence of anti-spike Abs was 97.4 %, 97.8 %, 97.4 % and 100 % in the infection group, CoronaVac group, ChAdOx1 group after 1st dose, and ChAdOx1 group after 2nd dose, respectively. Significantly higher levels of anti-spike Abs were observed in the ChAdOx1 group after two doses of vaccination (1975 AU/mL) compared to those who had recovered from natural infection (468.5 AU/mL) and individuals who had received CoronaVac (554.4 AU/mL). Neutralizing activity had a statistically significant positive correlation with levels of anti-spike Abs. CONCLUSIONS: ChAdOx1 vaccine may provide superior immunogenicity than CoronaVac and natural infection.
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spelling pubmed-101196722023-04-21 Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand Hongjaisee, Sayamon Chawansuntati, Kriangkrai Sripan, Patumrat Rattanathammethee, Kritsadee Sakkhachornphop, Supachai Chaiwarith, Romanee Sudjaritruk, Tavitiya Supparatpinyo, Khuanchai Wipasa, Jiraprapa Vaccine X Regular paper BACKGROUND: In Thailand, early vaccination initiatives for SARS-CoV-2 relied on CoronaVac (Sinovac Life Sciences) and ChAdOx1 (Oxford–AstraZeneca) vaccines. However, the data of immunogenicity of these two vaccines in Thai populations is limited. This real time, head-to-head comparative study was conducted to investigate antibody (Ab) responses to SARS-CoV-2 following infection or receipt of either CoronaVac or ChAdOx1 vaccination in Chiang Mai, Thailand. METHODS: Sera was collected within two months from participants having a history of documented SARS-CoV-2 infection or at one month after the second dose of CoronaVac vaccine. Sera from participants with a history of receiving one dose of ChAdOx1 vaccination was collected twice, at one month following each vaccine dose. Neutralizing antibodies (NAbs) were assessed using the surrogate neutralization test and anti-spike protein antibodies were assessed using an in-house enzyme-linked immunosorbent assay. RESULTS: The prevalence of NAbs against SARS-CoV-2 was 92.1 %, 95.7 %, 64.1 % and 100 % in the infection group, CoronaVac group, ChAdOx1 group after 1st dose, and ChAdOx1 group after 2nd dose, respectively. The inhibition rate in individuals receiving two doses of ChAdOx1 vaccine (90.8%) was significantly higher than individuals who had recovered from natural infection (71.7%) or individuals who had received two doses of CoronaVac vaccine (66.7%). The prevalence of anti-spike Abs was 97.4 %, 97.8 %, 97.4 % and 100 % in the infection group, CoronaVac group, ChAdOx1 group after 1st dose, and ChAdOx1 group after 2nd dose, respectively. Significantly higher levels of anti-spike Abs were observed in the ChAdOx1 group after two doses of vaccination (1975 AU/mL) compared to those who had recovered from natural infection (468.5 AU/mL) and individuals who had received CoronaVac (554.4 AU/mL). Neutralizing activity had a statistically significant positive correlation with levels of anti-spike Abs. CONCLUSIONS: ChAdOx1 vaccine may provide superior immunogenicity than CoronaVac and natural infection. Elsevier 2023-04-20 /pmc/articles/PMC10119672/ /pubmed/37155476 http://dx.doi.org/10.1016/j.jvacx.2023.100305 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular paper
Hongjaisee, Sayamon
Chawansuntati, Kriangkrai
Sripan, Patumrat
Rattanathammethee, Kritsadee
Sakkhachornphop, Supachai
Chaiwarith, Romanee
Sudjaritruk, Tavitiya
Supparatpinyo, Khuanchai
Wipasa, Jiraprapa
Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand
title Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand
title_full Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand
title_fullStr Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand
title_full_unstemmed Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand
title_short Comparison of antibody responses following natural infection with Severe Acute Respiratory Syndrome Coronavirus 2 or receipt of CoronaVac or ChAdOx1 (AZD1222) vaccination in Chiang Mai, Thailand
title_sort comparison of antibody responses following natural infection with severe acute respiratory syndrome coronavirus 2 or receipt of coronavac or chadox1 (azd1222) vaccination in chiang mai, thailand
topic Regular paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10119672/
https://www.ncbi.nlm.nih.gov/pubmed/37155476
http://dx.doi.org/10.1016/j.jvacx.2023.100305
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