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

卡介苗诱导的训练免疫可保护 K18-hACE2 小鼠免受 SARS-CoV-2 攻击。

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作者: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 ,Xuansheng Lin ,Xiner Huang ,Renhao Li ,Yee Man Au-Yeung ,Wenjun Li ,Bingjie Hu ,Yue Chai ,Ming Yue ,Jian-Piao Cai ,Guang Sheng Ling ,Ivan Fan-Ngai Hung ,Kwok-Yung Yuen ,Jasper Fuk-Woo Chan ,Jian-Dong Huang ,Hin Chu

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.

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