The Impact of Vaccination Time on the Antibody Response to an Inactivated Vaccine against SARS-CoV-2 (IMPROVE-2): A Randomized Controlled Trial.


Journal

Advanced biology
ISSN: 2701-0198
Titre abrégé: Adv Biol (Weinh)
Pays: Germany
ID NLM: 101775319

Informations de publication

Date de publication:
11 2023
Historique:
revised: 22 05 2023
received: 18 01 2023
medline: 22 11 2023
pubmed: 10 6 2023
entrez: 10 6 2023
Statut: ppublish

Résumé

There is still controversy about whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination at different times of day will induce a stronger immune response. Therefore, a randomized controlled trial (ChiCTR2100045109) is conducted to investigate the impact of vaccination time on the antibody response to the inactivated vaccine against SARS-CoV-2 from April 15 to 28, 2021. Participants are randomly assigned in a 1:1 ratio to receive inactivated SARS-CoV-2 vaccine in the morning or afternoon. The primary endpoint is the change of neutralizing antibody between baseline and 28 days after the second dose. In total, 503 participants are randomized, and 469 participants (238 in the morning group and 231 in the afternoon group) complete the follow-up. There is no significant difference in the change of neutralizing antibody between baseline and 28 days after the second dose between the morning and afternoon groups (22.2 [13.2, 45.0] AU mL

Identifiants

pubmed: 37300345
doi: 10.1002/adbi.202300028
doi:

Substances chimiques

COVID-19 Vaccines 0
Antibodies, Neutralizing 0
Vaccines, Inactivated 0

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2300028

Subventions

Organisme : Talent Program of First Affiliated Hospital of Sun Yat-Sen University
ID : Y70311
Organisme : National Natural Science Foundation of China
ID : 82103035
Organisme : Science and Technology Planning Project of Guangzhou
ID : 2022342

Informations de copyright

© 2023 Wiley-VCH GmbH.

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Auteurs

Fenghua Lai (F)

Department of Endocrinology, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Bin Li (B)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Jie Mei (J)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Qian Zhou (Q)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Jianyan Long (J)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Ruiming Liang (R)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Ruohui Mo (R)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Sui Peng (S)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Yihao Liu (Y)

Clinical Trials Unit, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

Haipeng Xiao (H)

Department of Endocrinology, The First Affiliated Hospital of Sun Yat-Sen University, No. 58, Zhongshan Road 2, Guangzhou, Guangdong, 510080, China.

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