Retrospective study of the immunogenicity and safety of the CoronaVac SARS-CoV-2 vaccine in people with underlying medical conditions
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Published:2022-11-25
Issue:1
Volume:2
Page:
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ISSN:2730-664X
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Container-title:Communications Medicine
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language:en
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Short-container-title:Commun Med
Author:
Li Chunmei, Bi Hanfang, Fu Zhenwang, Li Ao, Wan Na, Hu Jun, Yang Fan, Zhou Tai-Cheng, Liang Yupeng, Su Wei, Shi Tianpei, Yang Mei, Wang Rong, Qin Wanting, Yu Xuanjing, Zheng Hong-Yi, Zhou Zumi, Zheng Yong-TangORCID, Wei Jia, Zeng Gang, Zhang ZijieORCID, Chen Yanli, Yang Wei, Ma Xupu, Zhao Xinshuai, Jiang Xinyu, Wu Qingqin, Yan Yating, Xing Lei, Li Jingmei, Sun Lipei, Jiao Hanyi, Wu Junze, Liu Xueyan, Yu Houze, Dai Muxian, Liu Fengwei, Feng Muhua, Zhang Yuemiao, Wu Ying, You Dingyun, Wang Guo-Dong, Yan Guanghong, Xu Gangxu, Wang Yajing, Zhang Lihong, Zhang Liang,
Abstract
Abstract
Background
People living with chronic disease, particularly seniors (≥60 years old), made up of most severe symptom and death cases among SARS-CoV-2 infected patients. However, they are lagging behind in the national COVID-19 vaccination campaign in China due to the uncertainty of vaccine safety and effectiveness. Safety and immunogenicity data of COVID-19 vaccines in people with underlying medical conditions are needed to address the vaccine hesitation in this population.
Methods
We included participants (≥40 years old) who received two doses of CoronaVac inactivated vaccines (at a 3–5 week interval) and were healthy or had at least one of 6 common chronic diseases. The incidence of adverse events after vaccination was monitored. Vaccine immunogenicity was studied by determining neutralizing antibodies and SARS-CoV-2-specific T cell responses post vaccination.
Results
Here we show that chronic diseases are associated with a higher rate of mild fatigue following the first dose of CoronaVac. By day 14–28 post vaccination, the neutralizing antibody level shows no significant difference between disease groups and healthy controls, except for people with coronary artery disease (p = 0.0287) and chronic respiratory disease (p = 0.0416), who show moderate reductions. Such differences diminish by day 90 and 180. Most people show detectable SARS-CoV-2-specific T cell responses at day 90 and day 180 without significant differences between disease groups and healthy controls.
Conclusions
Our results highlight the comparable safety, immunogenicity and cellular immunity memory of CoronaVac in seniors and people living with chronic diseases. This data should reduce vaccine hesitancy in this population.
Funder
Yunnan Provincial Science and Technology Department Spring City Plan: the High-level Talent Promotion and Training Project of Kunming: This project funded by Kunming Science and Technology Bureau, Yunnan Province, China.
Publisher
Springer Science and Business Media LLC
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