An Observational Prospective Cohort Study of Vaccine Effectiveness Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection of an Aerosolized, Inhaled Adenovirus Type 5–Vectored Coronavirus Disease 2019 Vaccine Given as a Second Booster Dose in Guangzhou City, China

Author:

Wang Fu-Zhen1,Zhang Chun-Huan2,Tang Lin1,Rodewald Lance E1,Wang Wen2,Liu Si-Yu1,Wang Wen-Ji2,Wu Dan1,Liu Qian-Qian1,Wang Xiao-Qi1,Huang Li-Fang13,Huang Ao-Di1,Bao Li-Ming1,Zhang Zhou-Bin2,Yin Zun-Dong1ORCID

Affiliation:

1. National Immunization Program, Chinese Center for Disease Control and Prevention , Beijing, China

2. Department of Immunization Program Planning, Guangzhou Center for Disease Control and Prevention , Guangzhou, China

3. Department of Immunization Program, Fujian Provincial Center for Disease Control and Prevention , Fuzhou , China

Abstract

Abstract Using a prospective, observational cohort study during the post–“dynamic COVID-zero” wave in China, we estimated short-term relative effectiveness against Omicron BA.5 infection of inhaled aerosolized adenovirus type 5–vectored ancestral strain coronavirus disease 2019 (COVID-19) vaccine as a second booster dose approximately 1 year after homologous boosted primary series of inactivated COVID-19 vaccine compared with no second booster. Participants reported nucleic acid or antigen test results weekly until they tested positive or completed predesignated follow-up. After excluding participants infected <14 days after study entry, relative effectiveness among the 6576 participants was 61% in 18- to 59-year-olds and 38% in ≥60-year-olds and was sustained for 12 weeks.

Funder

Chinese Center for Disease Control and Prevention

National Key Research and Development Program

Emergency Key Program of Guangzhou Laboratory

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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