Targeting B cells enhances STING agonism in liver cancer

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Targeting B cells enhances STING agonism in liver cancer

Scientists have identified a promising strategy to improve liver cancer immunotherapy: targeting B-cells. While immunotherapy has transformed cancer treatment by activating T-cells—a type of immune cell that fights cancerous cells—many patients still fail to respond. New research shows that B-cells—another type of immune cells that fight infections—may play a surprising role in limiting immunotherapy’s effectiveness. 

The study was recently published in Nature Communications. The study’s principal investigator said that most current research efforts are focusing on activating T-cells against cancers. This study showed tumor-associated B-cells can create an environment that suppresses T-cell activity, allowing cancer cells to escape immune attacks.  

“We observed a significant rise in B-cell activity in the tumor, suggesting they may play an important role in how cancer escapes treatment,” said the author. “By blocking these immunosuppressive B-cells, we may be able to remove this barrier and enhance the power of immunotherapy.” 

The researchers used advanced laboratory and experimental models to uncover how B-cells contribute to immunotherapy resistance in liver cancer. Using liver  cancer mouse models, they tested treatments that either blocked B-cells or targeted immune pathways. 

They found that when tumors stopped responding to immunotherapy, B-cells moved into the tumor and formed clusters that looked like special immune structures called tertiary lymphoid tissues.

“Combining B-cell depletion with immunotherapy (anti-PD-1 ICB or the STING agonist BMS-986301) significantly improved survival and reduced metastasis,” said the author. “These exciting findings suggest that targeting B-cells or their signaling pathways could overcome acquired resistance and enhance the effectiveness of cancer immunotherapy, including in cases where the disease has spread.” 

The research also pinpoints the need for precision approaches—selectively targeting the B-cell subsets that drive resistance while preserving their beneficial roles in producing antibodies that fight diseases. 

https://www.nature.com/articles/s41467-025-66581-3

https://sciencemission.com/Inhibiting-B-cells