Evidence map›Paper›PMID 35446790›Full record

ArticleJCI insight2022

Bacillus Calmette-Guérin-induced trained immunity protects against SARS-CoV-2 challenge in K18-hACE2 mice.

Bao-Zhong Zhang, Huiping Shuai, Hua-Rui Gong, Jing-Chu Hu, Bingpeng Yan, Terrence Tsz-Tai Yuen, Ye-Fan Hu, Chaemin Yoon, Xiao-Lei Wang, Yuxin Hou and 15 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it, 65 citations in OpenAlex.

  1. Mucosal immunity and vaccine development.Signal transduction and targeted therapy · 2026
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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

25 authors at 5 institutions in 2 countries.

Bao-Zhong ZhangCAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Huiping ShuaiState Key Laboratory of Emerging Infectious Diseases, and.
Hua-Rui GongSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Jing-Chu HuCAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Bingpeng YanState Key Laboratory of Emerging Infectious Diseases, and.
Terrence Tsz-Tai YuenState Key Laboratory of Emerging Infectious Diseases, and.
Ye-Fan HuSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Chaemin YoonState Key Laboratory of Emerging Infectious Diseases, and.
Xiao-Lei WangSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Yuxin HouState Key Laboratory of Emerging Infectious Diseases, and.
Xuansheng LinSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Xiner HuangState Key Laboratory of Emerging Infectious Diseases, and.
Renhao LiSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Yee Man Au-YeungSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Wenjun LiCAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Bingjie HuState Key Laboratory of Emerging Infectious Diseases, and.
Yue ChaiState Key Laboratory of Emerging Infectious Diseases, and.
Ming YueSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Jian-Piao CaiState Key Laboratory of Emerging Infectious Diseases, and.
Guang Sheng LingSchool of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Ivan Fan-Ngai HungDepartment of Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Pokfulam, Hong Kong Special Administrative Region, China.
Kwok-Yung YuenState Key Laboratory of Emerging Infectious Diseases, and.
Jasper Fuk-Woo ChanState Key Laboratory of Emerging Infectious Diseases, and.
Jian-Dong HuangCAS Key Laboratory of Quantitative Engineering Biology, Shenzhen Institute of Synthetic Biology, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.
Hin ChuState Key Laboratory of Emerging Infectious Diseases, and.
Hong Kong Science and Technology Parks Corporation · HKUniversity of Hong Kong · HKChinese Academy of Sciences · CNSun Yat-sen University · CNUniversity of Hong Kong - Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 has been confirmed in over 450 million confirmed cases since 2019. Although several vaccines have been certified by the WHO and people are being vaccinated on a global scale, it has been reported that multiple SARS-CoV-2 variants can escape neutralization by antibodies, resulting in vaccine breakthrough infections. Bacillus Calmette-Guérin (BCG) is known to induce heterologous protection based on trained immune responses. Here, we investigated whether BCG-induced trained immunity protected against SARS-CoV-2 in the K18-hACE2 mouse model. Our data demonstrate that i.v. BCG (BCG-i.v.) vaccination induces robust trained innate immune responses and provides protection against WT SARS-CoV-2, as well as the B.1.617.1 and B.1.617.2 variants. Further studies suggest that myeloid cell differentiation and activation of the glycolysis pathway are associated with BCG-induced training immunity in K18-hACE2 mice. Overall, our study provides the experimental evidence that establishes a causal relationship between BCG-i.v. vaccination and protection against SARS-CoV-2 challenge.

Indexed as

COVID-19SARS-CoV-2AnimalsBCG Vaccinegamma-GlobulinsHumansMelphalanMiceBCG Vaccinegamma-GlobulinsK-18 conjugateMelphalanCOVID-19Infectious diseaseInnate immunity

Identifiers

PMID35446790
PMCPMC9220951
OpenAlexW4224293809

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.