JCI Insight (Jun 2022)

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,
  • 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

Journal volume & issue
Vol. 7, no. 11

Abstract

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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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