# TIR domain proteins: regulatory mechanisms in the tumor immune microenvironment, clinical translation strategies, and prospects for precision therapy applications

**Authors:** Jiatian Lou, Chenlei Gong, Xiaotao Gao, Jiaren Zhou, Qiyuan Wu, Xiaoliang Zheng, Liyan Cheng

PMC · DOI: 10.3389/fimmu.2025.1695754 · Frontiers in Immunology · 2025-12-18

## TL;DR

This review explores how TIR domain proteins regulate tumor immunity and discusses new strategies for combining TIR-targeted therapies with immunotherapies to improve cancer treatment.

## Contribution

The paper introduces novel combinatorial therapeutic strategies involving TIR agonists/inhibitors and immune checkpoint inhibitors for precision cancer immunotherapy.

## Key findings

- TIR domain proteins regulate both pro- and anti-tumor immune responses in the tumor microenvironment.
- Combining TIR-targeted therapies with nanodelivery systems and radiotherapy may enhance treatment efficacy and reduce toxicity.
- TIR proteins show promise as precision therapy targets for improving cancer immunotherapy outcomes.

## Abstract

Toll/IL-1R (TIR) domain proteins, as central signaling hubs in innate immunity, dynamically orchestrate inflammatory responses and immune processes within the tumor microenvironment (TME) by mediating both MyD88-dependent and TRIF-dependent pathways. This review systematically elaborates on the dual regulatory roles of the TIR superfamily-encompassing toll-like receptors (TLRs), IL-1 receptors (IL-1Rs), and adaptor proteins-in tumor immunity, including the facilitation of stemness maintenance in cancer stem cells (CSCs) and the inductive mechanisms driving the formation of an immunosuppressive TME. From the perspective of clinical translation, the combinatorial therapeutic strategy of TIR agonists/inhibitors with immune checkpoint inhibitors (ICIs) represents a novel paradigm: the synergistic effects among TIR agonists/inhibitors, advanced nanodelivery systems, and radiotherapy-responsive prodrug technology provide a potential approach to address challenges such as systemic toxicity and low targeted delivery efficiency. Looking forward, the continuous advancement and broader application of TIR protein targets in the field of precision cancer immunotherapy hold great promise for offering new hope in the fight against malignant tumors.

## Linked entities

- **Proteins:** MYD88 (MYD88 innate immune signal transduction adaptor), TRIM69 (tripartite motif containing 69)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** TICAM1 (TIR domain containing adaptor molecule 1) [NCBI Gene 148022] {aka IIAE6, MyD88-3, PRVTIRB, TICAM-1, TRIF}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}
- **Diseases:** inflammatory (MESH:D007249), cancer (MESH:D009369), toxicity (MESH:D064420)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12756155/full.md

## References

249 references — full list in the complete paper: https://tomesphere.com/paper/PMC12756155/full.md

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Source: https://tomesphere.com/paper/PMC12756155