Microbial cancer immunotherapy reprograms hematopoiesis to enhance myeloid-driven anti-tumor immunity.

TitleMicrobial cancer immunotherapy reprograms hematopoiesis to enhance myeloid-driven anti-tumor immunity.
Publication TypeJournal Article
Year of Publication2025
AuthorsDaman AW, Antonelli AC, Redelman-Sidi G, Paddock L, Khayat S, Ketavarapu M, Cheong JGyu, Jurado LF, Benjamin A, Jiang S, Ahimovic D, Lawless VR, Bale MJ, Loutochin O, McPherson VA, Divangahi M, Niec RE, Pe'er D, Pietzak E, Josefowicz SZ, Glickman MS
JournalCancer Cell
Volume43
Issue8
Pagination1442-1459.e10
Date Published2025 Aug 11
ISSN1878-3686
Abstract

Mycobacterium bovis Bacillus Calmette-Guérin (BCG) is the vaccine against tuberculosis and an immunotherapy for bladder cancer. When administered intravenously, BCG reprograms bone marrow hematopoietic stem and progenitor cells (HSPCs), leading to heterologous protection against infections. Whether HSPC reprogramming contributes to the anti-tumor effects of BCG administered into the bladder is unknown. We demonstrate that BCG administered in the bladder colonizes the bone marrow and, in both mice and humans, reprograms HSPCs to alter and amplify myelopoiesis. BCG-reprogrammed HSPCs are sufficient to confer augmented anti-tumor immunity through production of neutrophils, monocytes, and dendritic cells that broadly remodel the tumor microenvironment, drive T cell-dependent anti-tumor responses, and synergize with checkpoint blockade. We conclude that bladder BCG acts systemically through hematopoiesis, highlighting the broad potential of HSPC reprogramming to enhance the innate drivers of T cell-dependent tumor immunity.

DOI10.1016/j.ccell.2025.05.002
Alternate JournalCancer Cell
PubMed ID40446799
Grant ListT32 CA260293 / CA / NCI NIH HHS / United States

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