# Role of microbiota in the outcome of immune checkpoint inhibition therapy of cancer

**Authors:** Ger T. Rijkers, Yonah Langcauon, Pippe van Leersum, Lara Popović, Frans J. van Overveld

PMC · DOI: 10.37349/etat.2025.1002348 · Exploration of Targeted Anti-tumor Therapy · 2025-11-18

## TL;DR

Gut microbiota influences cancer treatment outcomes, and understanding its role could improve immune therapy effectiveness.

## Contribution

The paper highlights how gut microbiota can be manipulated to enhance immune checkpoint inhibition therapy for cancer.

## Key findings

- Fecal microbiota transplantation can improve immune checkpoint inhibition therapy outcomes.
- Certain gut bacteria can promote or inhibit tumor growth, affecting treatment success.
- Microbiota can colonize the tumor microenvironment, influencing immune responses.

## Abstract

The realization that the composition and functionality of gut microbiota have an impact on the outcome of immune checkpoint inhibition (ICI) therapy of cancer has initiated research into the potential of microbiota management as adjunctive therapy. Fecal microbiota transplantation can improve the outcome of ICI, but for optimal donor selection, safety, and large-scale implementation, there remain bottlenecks. Alternative strategies, such as the use of selected bacterial species, require fundamental knowledge of the underlying mechanisms governing the interaction between (intestinal) microbiota and the immune system. Gut microbiota also appears to be able to colonize the tumor microenvironment. Some bacterial species directly or indirectly promote tumor growth. Other defined species have tumoricidal properties. These findings and insights are now being used to further optimize the functionality of the immune system and shape the tumor microenvironment in order to improve the outcome of ICI.

## Linked entities

- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Diseases:** cancer (MESH:D009369)

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12635439/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12635439/full.md

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Source: https://tomesphere.com/paper/PMC12635439