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

IF 2.7 Q3 IMMUNOLOGY Vaccine: X Pub Date : 2024-03-16 DOI:10.1016/j.jvacx.2024.100475
Kriangkrai Chawansuntati , Supachai Sakkhachornphop , Sayamon Hongjaisee , Saranta Freeouf , Patumrat Sripan , Nattaya Nusartsang , Romanee Chaiwarith , Tavitiya Sudjaritruk , Khuanchai Supparatpinyo , Jiraprapa Wipasa
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Abstract

Background

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

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

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

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.

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CoronaVac 和 ChAdOx1 异源原代强化疫苗在泰国清迈超重人群中的安全性和免疫原性
背景2021年初,泰国公共卫生部公布了COVID-19疫苗的异源接种方案,首剂为CoronaVac,随后接种ChAdOx1 nCoV-19,间隔3周。60岁以上和患有肥胖症等七种基础疾病的人优先接种。在泰国清迈的超重人群中对该疫苗方案的安全性和免疫原性进行了评估。在每次免疫接种前和第二次接种后的第 28 天采集血液样本,并通过间接 ELISA 和病毒中和试验检测抗尖峰抗体和中和抗体。研究期间未报告与疫苗接种相关的严重不良反应,大多数不良反应为疲劳和注射部位疼痛。基线、第一剂接种后 21 天和第二剂接种后 28 天的抗穗IgG水平分别为 26.3、56.4 和 1752.1 BAU/mL。完全接种后 4 周,通过代用中和检测法测定的针对野生型、Delta 型和 Omicron 型变体的中和抗体抑制率中位数分别为 95.2、85.0 和 3.8。此外,通过伪型病毒中和试验测定的野生型和 Delta 变体的 NT50 水平分别为 133.3 和 41.7。结论 在超重人群中,异源 CoronaVac-ChAdOx1 疫苗接种安全、耐受性良好,能够诱导针对野生型和 Delta 变异型的体液免疫,但不能诱导针对 Omicron 变异型的体液免疫。
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来源期刊
Vaccine: X
Vaccine: X Multiple-
CiteScore
2.80
自引率
2.60%
发文量
102
审稿时长
13 weeks
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