Journal
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 117, Issue 38, Pages 23674-23683Publisher
NATL ACAD SCIENCES
DOI: 10.1073/pnas.2010981117
Keywords
IgA; type I IFN signaling; circulation between gut and periphery; gut-microbiota education; mitochondrial activation
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Funding
- Japan Agency for Medical Research and Development (AMED) [JP19gm0710012, JP19cm0106302, JP19gm6110019]
- Tang Prize Foundation
- Japan Society for the Promotion of Science (JSPS) KAKENHI [JP16H06149]
- Honjo International Scholarship Foundation
- MEXT scholarship
- BristolMyers Squibb
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The gut microbiome has garnered attention as an effective target to boost immunity and improve cancer immunotherapy. We found that B cell-defective (BCD) mice, such as mu-membrane targeted deletion (mu MT) and activation-induced cytidine deaminase (AID) knockouts (KOs), have elevated antitumor immunity under specific pathogen-free but not germ-free conditions. Microbial dysbiosis in these BCD mice enriched the type I IFN (IFN) signature in mucosal CD8(+) T cells, resulting in up-regulation of the type I IFN-inducible protein stem cell antigen-1 (Sca-1). Among CD8(+) T cells, naive cells predominantly circulate from the gut to the periphery, and those that had migrated from the mesenteric lymph nodes (mLNs) to the periphery had significantly higher expression of Sca-1. The gut-educated Sca-1(+) naive subset is endowed with enhanced mitochondrial activity and antitumor effector potential. The heterogeneity and functional versatility of the systemic naive CD8(+) T cell compartment was revealed by single-cell analysis and functional assays of CD8(+) T cell subpopulations. These results indicate one of the potential mechanisms through which microbial dysbiosis regulates antitumor immunity.
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