Safety and immunogenicity of CoronaVac and ChAdOx1 heterologous prime-boost vaccines in an overweight population in Chiang Mai, Thailand.

ChAdOx1 CoronaVac Coronavirus disease (COVID-19) Neutralizing antibodies Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2)

Journal

Vaccine: X
ISSN: 2590-1362
Titre abrégé: Vaccine X
Pays: England
ID NLM: 101748769

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 20 07 2023
revised: 13 03 2024
accepted: 15 03 2024
medline: 29 3 2024
pubmed: 29 3 2024
entrez: 29 3 2024
Statut: epublish

Résumé

In early 2021, the Ministry of Public Health of Thailand announced heterologous regimens for COVID-19 vaccines using CoronaVac as the first dose followed by ChAdOx1 nCoV-19 at 3 weeks apart. Priority was given to individuals above 60 years old and those who had seven underlying conditions, including obesity. The vaccine regimen was evaluated for safety and immunogenicity in overweight populations in Chiang Mai, Thailand. Participants who had a COVID-19 vaccination appointment for the heterologous prime-boost regimen were enrolled. Before each immunization and on day 28 following the second dosage, blood samples were taken, and were examined for anti-spike and neutralizing antibodies by using an indirect ELISA and virus neutralization assays. Safety profile of the vaccine regimen was assessed via a self-recorded diary of adverse events after each vaccination. No serious adverse events related to vaccination were reported during study period and the majority of adverse reactions were fatigue and pain at the injection site. The levels of anti-spike IgG were 26.3, 56.4 and 1752.1 BAU/mL at baseline, 21 days after first dose and 28 days after second dose, respectively. At 4 weeks after complete vaccination, the median inhibition rates of neutralizing antibody determined by surrogate neutralization assay against wild type, Delta and Omicron variants were 95.2, 85.0 and 3.8, respectively. Moreover, the NT50 level against wild type and Delta variants determined by pseudotyped virus neutralization assay were 133.3 and 41.7, respectively. The neutralizing activity against Omicron variant was almost lower than cutoff level for detection. The heterologous CoronaVac-ChAdOx1vaccination was safe, well-tolerated and able to induce humoral immunity against wild-type and Delta variants but not against the Omicron variant in overweight population.

Sections du résumé

Background UNASSIGNED
In early 2021, the Ministry of Public Health of Thailand announced heterologous regimens for COVID-19 vaccines using CoronaVac as the first dose followed by ChAdOx1 nCoV-19 at 3 weeks apart. Priority was given to individuals above 60 years old and those who had seven underlying conditions, including obesity. The vaccine regimen was evaluated for safety and immunogenicity in overweight populations in Chiang Mai, Thailand.
Methods UNASSIGNED
Participants who had a COVID-19 vaccination appointment for the heterologous prime-boost regimen were enrolled. Before each immunization and on day 28 following the second dosage, blood samples were taken, and were examined for anti-spike and neutralizing antibodies by using an indirect ELISA and virus neutralization assays. Safety profile of the vaccine regimen was assessed via a self-recorded diary of adverse events after each vaccination.
Results UNASSIGNED
No serious adverse events related to vaccination were reported during study period and the majority of adverse reactions were fatigue and pain at the injection site. The levels of anti-spike IgG were 26.3, 56.4 and 1752.1 BAU/mL at baseline, 21 days after first dose and 28 days after second dose, respectively. At 4 weeks after complete vaccination, the median inhibition rates of neutralizing antibody determined by surrogate neutralization assay against wild type, Delta and Omicron variants were 95.2, 85.0 and 3.8, respectively. Moreover, the NT50 level against wild type and Delta variants determined by pseudotyped virus neutralization assay were 133.3 and 41.7, respectively. The neutralizing activity against Omicron variant was almost lower than cutoff level for detection.
Conclusions UNASSIGNED
The heterologous CoronaVac-ChAdOx1vaccination was safe, well-tolerated and able to induce humoral immunity against wild-type and Delta variants but not against the Omicron variant in overweight population.

Identifiants

pubmed: 38549951
doi: 10.1016/j.jvacx.2024.100475
pii: S2590-1362(24)00048-2
pmc: PMC10973674
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100475

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Kriangkrai Chawansuntati (K)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Supachai Sakkhachornphop (S)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Sayamon Hongjaisee (S)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Saranta Freeouf (S)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Patumrat Sripan (P)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Nattaya Nusartsang (N)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Romanee Chaiwarith (R)

Division of Infectious Diseases and Tropical Medicine, Department of Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai 50202, Thailand.

Tavitiya Sudjaritruk (T)

Division of Infectious Diseases, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai 50202, Thailand.

Khuanchai Supparatpinyo (K)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Jiraprapa Wipasa (J)

Research Institute for Health Sciences, Chiang Mai University, Chiang Mai 50202, Thailand.

Classifications MeSH