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

TitleBacillus Calmette-Guérin–induced trained immunity protects against SARS-CoV-2 challenge in K18-hACE2 mice
Authors
Issue Date2022
Citation
JCI Insight, 2022, v. 7, n. 11, article no. e157393 How to Cite?
AbstractSARS-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.
Persistent Identifierhttp://hdl.handle.net/10722/315398
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, Bao Zhong-
dc.contributor.authorShuai, Huiping-
dc.contributor.authorGong, Hua Rui-
dc.contributor.authorHu, Jing Chu-
dc.contributor.authorYan, Bingpeng-
dc.contributor.authorYuen, Terrence Tsz Tai-
dc.contributor.authorHu, Ye Fan-
dc.contributor.authorYoon, Chaemin-
dc.contributor.authorWang, Xiao Lei-
dc.contributor.authorHou, Yuxin-
dc.contributor.authorLin, Xuansheng-
dc.contributor.authorHuang, Xiner-
dc.contributor.authorLi, Renhao-
dc.contributor.authorAu-Yeung, Yee Man-
dc.contributor.authorLi, Wenjun-
dc.contributor.authorHu, Bingjie-
dc.contributor.authorChai, Yue-
dc.contributor.authorYue, Ming-
dc.contributor.authorCai, Jian Piao-
dc.contributor.authorLing, Guang Sheng-
dc.contributor.authorHung, Ivan Fan Ngai-
dc.contributor.authorYuen, Kwok Yung-
dc.contributor.authorChan, Jasper Fuk Woo-
dc.contributor.authorHuang, Jian Dong-
dc.contributor.authorChu, Hin-
dc.date.accessioned2022-08-05T10:18:45Z-
dc.date.available2022-08-05T10:18:45Z-
dc.date.issued2022-
dc.identifier.citationJCI Insight, 2022, v. 7, n. 11, article no. e157393-
dc.identifier.urihttp://hdl.handle.net/10722/315398-
dc.description.abstractSARS-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.-
dc.languageeng-
dc.relation.ispartofJCI Insight-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleBacillus Calmette-Guérin–induced trained immunity protects against SARS-CoV-2 challenge in K18-hACE2 mice-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1172/jci.insight.157393-
dc.identifier.pmid35446790-
dc.identifier.pmcidPMC9220951-
dc.identifier.scopuseid_2-s2.0-85131770741-
dc.identifier.volume7-
dc.identifier.issue11-
dc.identifier.spagearticle no. e157393-
dc.identifier.epagearticle no. e157393-
dc.identifier.eissn2379-3708-
dc.identifier.isiWOS:000810851500001-

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