Evidence map›Paper›PMID 35850623›Full record

ArticleEmerging microbes & infections2022

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 Wu, Ying Ye, Lin Tang, Ai-Bin Wang, Rui Zhang, Zhao-Hui Qian, Fu-Zhen Wang, Hui Zheng, Chang Huang, Xiao-Ya Lv and 13 more

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 4 countries.

Dan WuNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Ying YeHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Lin TangNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Ai-Bin WangBeijing Ditan Hospital, Capital Medical University, Beijing, People's Republic of China.
Rui ZhangNational Center for Clinical Laboratories, Beijing Hospital, National Center of Gerontology, Institute of Geriatric Medicine, Chinese Academy of Medical Sciences, Beijing, People's Republic of China.
Zhao-Hui QianNHC Key laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People's Republic of China.
Fu-Zhen WangNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Hui ZhengNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Chang HuangChinese Field Epidemiology Training Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Xiao-Ya LvDevelopment Center for Medicine and Science &Technology, National Health Commission, People's Republic of China, Beijing.
Hai-Feng WangHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Yan-Yang ZhangHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Jing-Jing PanHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Ya-Fei LiHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Ming-Xia LuHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Chang-Shuang WangHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Ya-Ting MaHenan Provincial Disease Control and Prevention, People's Republic of China, Henan.
Zhi-Jie AnNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Lance Everett RodewaldNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Zun-Dong YinNational Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Xuan-Yi WangKey Laboratory of Medical Molecular Virology of MoE & MoH, Shanghai Institute of Infectious Disease and Biosecurity, Shanghai, People's Republic of China.ORCID 0000-0001-6398-9184
Zhi-Yin WuDevelopment Center for Medicine and Science &Technology, National Health Commission, People's Republic of China, Beijing.
Yi-Ming ShaoState Key Laboratory of Infectious Disease Prevention and Control, National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, People's Republic of China.
Chinese Center For Disease Control and Prevention · CNHenan Provincial Center for Disease Control and Prevention · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNNational Health and Family Planning Commission · CNCapital Medical University · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

COVID-19PneumoniaChinaCOVID-19 VaccinesHumansImmunization, SecondarySARS-CoV-2Viral LoadCOVID-19 Vaccinesbooster immunizationcase-case studyCOVID-19 vaccineCt valuereal-world study

Identifiers

PMID35850623
PMCPMC9359169
OpenAlexW4285797164

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.