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Pre-exposure to mRNA-LNP inhibits adaptive immune responses and alters innate immune fitness in an inheritable fashion

Zhen Qin, Aurélie Bouteau, Christopher Herbst, Botond Z. Igyártó
doi: https://doi.org/10.1101/2022.03.16.484616
Zhen Qin
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, U.S.
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Aurélie Bouteau
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, U.S.
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Christopher Herbst
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, U.S.
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Botond Z. Igyártó
Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA 19107, U.S.
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  • For correspondence: botond.igyarto@jefferson.edu
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ABSTRACT

Hundreds of millions of SARS-CoV-2 mRNA-LNP vaccine doses have already been administered to humans. However, we lack a comprehensive understanding of the immune effects of this platform. The mRNA-LNP-based SARS-CoV-2 vaccine is highly inflammatory, and its synthetic ionizable lipid component responsible for the induction of inflammation has a long in vivo half-life. Since chronic inflammation can lead to immune exhaustion and non-responsiveness, we sought to determine the effects of pre-exposure to the mRNA-LNP on adaptive immune responses and innate immune fitness. We found that pre-exposure to mRNA-LNPs or LNP alone led to long-term inhibition of the adaptive immune responses, which could be overcome using standard adjuvants. On the other hand, we report that after pre-exposure to mRNA-LNPs, the resistance of mice to heterologous infections with influenza virus increased while Candida albicans decreased. The diminished resistance to Candida albicans correlated with a general decrease in blood neutrophil percentages. Interestingly, mice pre-exposed to the mRNA-LNP platform can pass down the acquired immune traits to their offspring, providing better protection against influenza. In summary, the mRNA-LNP vaccine platform induces long-term unexpected immunological changes affecting both adaptive immune responses and heterologous protection against infections. Thus, our studies highlight the need for more research to determine this platform’s true impact on human health.

Authors Summary We bring experimental evidence that pre-exposure to mRNA-LNPs or its LNP component affects innate and adaptive immune responses. Pre-exposure to mRNA-LNPs led to long-term inhibition of the adaptive immune responses, which the use of adjuvants could overcome. On the other hand, we report that after pre-exposure to mRNA-LNPs, the resistance of mice to heterologous infections with influenza virus increased while Candida albicans decreased. We also detected a general neutropenia in the mRNA-LNP exposed mice. Interestingly, mice pre-exposed to mRNA-LNPs can pass down the acquired immune traits to their offspring. In summary, the mRNA-LNP vaccine platform induces long-term immunological changes that can affect both adaptive immune responses and heterologous protection against infections, some of which can be inherited by the offspring. More studies are needed to understand the mechanisms responsible for these effects and determine this platform’s impact on human health.

Competing Interest Statement

The authors have declared no competing interest.

Footnotes

  • The revision includes revised Candida data and several extra figures.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted August 20, 2022.
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Pre-exposure to mRNA-LNP inhibits adaptive immune responses and alters innate immune fitness in an inheritable fashion
Zhen Qin, Aurélie Bouteau, Christopher Herbst, Botond Z. Igyártó
bioRxiv 2022.03.16.484616; doi: https://doi.org/10.1101/2022.03.16.484616
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Pre-exposure to mRNA-LNP inhibits adaptive immune responses and alters innate immune fitness in an inheritable fashion
Zhen Qin, Aurélie Bouteau, Christopher Herbst, Botond Z. Igyártó
bioRxiv 2022.03.16.484616; doi: https://doi.org/10.1101/2022.03.16.484616

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