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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.

Dan WuYing YeLin TangAi-Bin WangRui ZhangZhao-Hui QianFu-Zhen WangHui ZhengChang HuangXiao-Ya LvHai-Feng WangYan-Yang ZhangJing-Jing PanYa-Fei LiMing-Xia LuChang-Shuang WangYa-Ting MaZhi-Jie AnLance Everett RodewaldZun-Dong YinXuan-Yi WangZhi-Yin WuYi-Ming Shao
Published in: Emerging microbes & infections (2022)
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.
Keyphrases
  • sars cov
  • coronavirus disease
  • computed tomography
  • magnetic resonance imaging
  • intensive care unit
  • dna methylation
  • community acquired pneumonia
  • image quality
  • respiratory failure
  • genome wide
  • mechanical ventilation