Presence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Antibodies Among Vietnamese Healthcare Workers by Dosing Interval for ChAdOx1 nCoV-19 Vaccine

Abstract Background Before the SARS-CoV-2 Delta variant arrived in Vietnam, case rates suggested seroprevalence of SARS-CoV-2 was low. Beginning in March 2021, we assessed different dosing schedules and adverse events following immunization (AEFIs) for ChAdOx1 nCoV-19 vaccine among healthcare worker...

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Veröffentlicht in:Clinical infectious diseases 2022-10, Vol.75 (Supplement_2), p.S174-S181
Hauptverfasser: Vu, Dien M, Vu, Diep T B, Do, Thuy T T, Olmsted, Allison E, Dao, Bach H, Thai, Truc T, Nguyen, Chi L, Le, Nhung T T, Le, Tuan A, Bui, Hien T T, Pham, Thach N, Moore, Matthew R
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Sprache:eng
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Zusammenfassung:Abstract Background Before the SARS-CoV-2 Delta variant arrived in Vietnam, case rates suggested seroprevalence of SARS-CoV-2 was low. Beginning in March 2021, we assessed different dosing schedules and adverse events following immunization (AEFIs) for ChAdOx1 nCoV-19 vaccine among healthcare workers (HCWs). Methods We performed a prospective cohort study to estimate the prevalence of IgG antibodies to SARS-CoV-2 before and after ChAdOx1 nCoV-19 vaccination. We conducted antibody testing among HCWs in February 2021 (baseline), before the second dose (June–July 2021), and 1 and 3 months after the second dose. We detected antibodies to SARS-CoV-2 using Tetracore® FlexImmArray™, and surrogate neutralizing antibodies using GenScript cPass™. Neither assay can distinguish natural from vaccine-induced antibodies. We assessed AEFIs through interview post–dose 1 and 1 month post–dose 2. Results Before vaccination, 1/617 participants (0.16%) had antibodies to SARS-CoV-2. Of these 617, 405 were vaccinated with ChAdOx1 nCoV-19 with 4–8- (60%), 9–12- (27%), or ≥13-week (13%) intervals between the 2 doses. Three months following series completion, 99% and 97% of vaccinated participants had ≥1 sample with detectable antibodies and surrogate neutralizing antibodies against SARS-CoV-2, respectively. We observed no significant differences among those with different dosing intervals at last follow-up. All participants reported PCR testing for SARS-CoV-2 during the study; 2 (0.5%) were laboratory-confirmed. AEFIs were more frequent post–dose 1 (81%) vs post–dose 2 (21%). Conclusions In this population, regardless of dosing interval, ChAdOx1 nCoV-19 induced antibodies within 3 months of the second dose. These findings may offer flexibility to policymakers when balancing programmatic considerations with vaccine effectiveness. SARS-CoV-2 antibody prevalence was estimated among members of a prospective cohort of Vietnamese healthcare workers receiving 2 doses of ChAdOx1 nCoV-19 vaccine. ChAdOx1 nCoV-19 vaccine appears effective in provoking an antibody response with similar effects for different dosing intervals.
ISSN:1058-4838
1537-6591
DOI:10.1093/cid/ciac493