A case-case study on the effect of primary and booster immunization with China-produced COVID-19 vaccines on prevention of pneumonia and viral load among vaccinated persons infected by Delta and Omicron variants

被引:4
作者
Wu, Dan [1 ]
Ye, Ying [2 ]
Tang, Lin [1 ]
Wang, Ai-Bin [3 ]
Zhang, Rui [4 ]
Qian, Zhao-Hui [5 ]
Wang, Fu-Zhen [1 ]
Zheng, Hui [1 ]
Huang, Chang [6 ,7 ]
Lv, Xiao-Ya [8 ]
Wang, Hai-Feng [2 ]
Zhang, Yan-Yang [2 ]
Pan, Jing-Jing [2 ]
Li, Ya-Fei [2 ]
Lu, Ming-Xia [2 ]
Wang, Chang-Shuang [2 ]
Ma, Ya-Ting [2 ]
An, Zhi-Jie [1 ]
Rodewald, Lance Everett [1 ]
Yin, Zun-Dong [1 ]
Wang, Xuan-Yi [9 ,10 ]
Wang, Xuan-Yi [9 ,10 ]
Wu, Zhi-Yin [8 ]
Shao, Yi-Ming [11 ]
机构
[1] Chinese Ctr Dis Control & Prevent, Natl Immunizat Program, 27 Nanwei Rd, Beijing, Peoples R China
[2] Henan Prov Dis Control & Prevent, Zhengzhou, Henan, Peoples R China
[3] Capital Med Univ, Beijing Ditan Hosp, Beijing, Peoples R China
[4] Chinese Acad Med Sci, Natl Ctr Clin Labs, Beijing Hosp, Natl Ctr Gerontol,Inst Geriatr Med, Beijing, Peoples R China
[5] Chinese Acad Med Sci & Peking Union Med Coll, Inst Pathogen Biol, NHC Key Lab Syst Biol Pathogens, Beijing, Peoples R China
[6] Chinese Ctr Dis Control & Prevent, Chinese Field Epidemiol Training Program, Beijing, Peoples R China
[7] Nanning Ctr Dis Control & Prevent, Nanning, Guangxi, Peoples R China
[8] Natl Hlth Commiss, Dev Ctr Med & Sci & Technol, 9 Chegongzhuang St, Beijing, Peoples R China
[9] Shanghai Inst Infect Dis & Biosecur, Key Lab Med Mol Virol MoE & MoH, Shanghai, Peoples R China
[10] Fudan Univ, Shanghai Med Coll, Inst Biomed Sci, 138 Yi Xue Yuan Rd, Shanghai, Peoples R China
[11] Chinese Ctr Dis Control & Prevent, Natl Ctr AIDS STD Control & Prevent, State Key Lab Infect Dis Prevent & Control, Beijing, Peoples R China
关键词
COVID-19; vaccine; Ct value; case-case study; real-world study; booster immunization; HOSPITALIZATIONS; ADULTS;
D O I
10.1080/22221751.2022.2103455
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Using a three-prefecture, two-variant COVID-19 outbreak in Henan province in January 2022, we evaluated the associations of primary and booster immunization with China-produced COVID-19 vaccines and COVID-19 pneumonia and SARS-CoV-2 viral load among persons infected by Delta or Omicron variant. We obtained demographic, clinical, vaccination, and multiple Ct values of infections >= 3 years of age. Vaccination status was either primary series >= 180 days prior to infection; primary series <180 days prior to infection, or booster dose recipient. We used logistic regression to determine odds ratios (OR) of Delta and Omicron COVID-19 pneumonia by vaccination status. We analysed minimum Ct values by vaccination status, age, and variant. Of 826 eligible cases, 405 were Delta and 421 were Omicron cases; 48.9% of Delta and 19.0% of Omicron cases had COVID-19 pneumonia. Compared with full primary vaccination >= 180 days before infection, the aOR of pneumonia was 0.48 among those completing primary vaccination <180 days and 0.18 among booster recipients among these Delta infections. Among Omicron infections, the corresponding aOR was 0.34 among those completing primary vaccination <180 days. There were too few (ten) Omicron cases among booster dose recipients to calculate a reliable OR. There were no differences in minimum Ct values by vaccination status among the 356 Delta cases or 70 Omicron cases. COVID-19 pneumonia was less common among Omicron cases than Delta cases. Full primary vaccination reduced pneumonia effectively for 6 months; boosting six months after primary vaccination resulted in further reduction. We recommend accelerating the pace of booster dose administration.
引用
收藏
页码:1950 / 1958
页数:9
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