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Updated: Sep 9, 2025

Ex vivo Expansion of Tumor-reactive T Cells by Means of Bryostatin 1/Ionomycin and the Common Gamma Chain Cytokines Formulation
Published on: January 14, 2011
Bifidobacteria-derived exopolysaccharide promotes anti-tumor immunity
Rômulo Silva de Oliveira1, Amy Shupe2, Tim Krause3
1M3 Research Center, Faculty of Medicine, University of Tübingen, Tübingen, Germany; Department of Internal Medicine I, Faculty of Medicine, University of Tübingen, Tübingen, Germany; Cluster of Excellence EXC 2124 Controlling Microbes to Fight Infections, University of Tübingen, Tübingen, Germany.
None:
While several phylogenetically distinct bacterial taxa can predict responses to or improve cancer immunotherapies, the underlying mechanisms remain poorly understood. The use of microbes for microbial therapeutics is currently under intense research, yet safety and regulatory hurdles remain challenging. Thus, non-replicative bacterial-derived molecules or extracts provide promising alternatives. We have identified exopolysaccharides (EPSs) from two bacterial species-Bifidobacterium pseudolongum and Bifidobacterium pseudocatenulatum-that promote anti-tumor immunity. EPS improved Th1 T cell immunity, which was further boosted by the metabolite inosine. Mechanistically, EPS was sensed by dendritic cells in a Tlr2-MyD88-dependent manner, which induced interleukin (IL)-12 and tumor necrosis factor (TNF)-α. Both cytokines were required for T cell-dependent killing of tumor cells in murine colon cancer models. EPS stimulated IL-12 production through Toll-like receptor 2 (TLR2) in human dendritic cells and promoted cell death in patient-derived colon cancer organoids through immune cells. Collectively, our study identifies microbe-derived EPS as an adjuvant immunotherapy in cancer.
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