Combined GPR81 Blockade and STING Agonism Restore CD8⁺ T Cell–Mediated Tumor Control in Triple-Negative Breast Cancer

Triple-negative breast cancer (TNBC) creates an immunosuppressive tumor microenvironment (TME) that limits the efficacy of checkpoint immunotherapy. Tumor-derived lactate activates GPR81 signaling on tumor-associated macrophages (TAMs), while the STING pathway, which normally drives innate immune activation, remains suppressed, together maintaining TAMs in an immunosuppressive state and limiting CD8⁺ T cell activity. This study aims to test whether combined GPR81 blockade and STING activation can synergistically repolarize TAMs and restore CD8⁺ T cell–mediated tumor control. Using a syngeneic 4T1 mouse model of TNBC, we will compare vehicle, single-agent, and combination treatment groups, alongside genetic GPR81 deletion and CD8⁺ T cell depletion to establish pathway specificity. We predict combination therapy will produce greater macrophage repolarization, CD8⁺ T cell infiltration, and tumor regression than either agent alone. These findings would support dual metabolic and innate immune targeting as a strategy to overcome immunotherapy resistance in breast cancer.

Authors

Institutions

Publication Details

Journal
Theoretical and Natural Science
Published
2026-10-27
DOI
https://doi.org/10.54254/2753-8818/2026.38136
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Combined GPR81 Blockade and STING Agonism Restore CD8⁺ T Cell–Mediated Tumor Control in Triple-Negative Breast Cancer

Kevin Yang, Sungjae Lee, Rain Lin, Qingyu Che et al.
2 links
Theoretical and Natural Science
Immune cells in cancer
article

Combined GPR81 Blockade and STING Agonism Restore CD8⁺ T Cell–Mediated Tumor Control in Triple-Negative Breast Cancer

Kevin Yang, Sungjae Lee, Rain Lin, Qingyu Che, Alex Pang
article en

Abstract

Triple-negative breast cancer (TNBC) creates an immunosuppressive tumor microenvironment (TME) that limits the efficacy of checkpoint immunotherapy. Tumor-derived lactate activates GPR81 signaling on tumor-associated macrophages (TAMs), while the STING pathway, which normally drives innate immune activation, remains suppressed, together maintaining TAMs in an immunosuppressive state and limiting CD8⁺ T cell activity. This study aims to test whether combined GPR81 blockade and STING activation can synergistically repolarize TAMs and restore CD8⁺ T cell–mediated tumor control. Using a syngeneic 4T1 mouse model of TNBC, we will compare vehicle, single-agent, and combination treatment groups, alongside genetic GPR81 deletion and CD8⁺ T cell depletion to establish pathway specificity. We predict combination therapy will produce greater macrophage repolarization, CD8⁺ T cell infiltration, and tumor regression than either agent alone. These findings would support dual metabolic and innate immune targeting as a strategy to overcome immunotherapy resistance in breast cancer.

Theoretical and Natural ScienceVol. 201(1)
Ste. Anne's Hospital (CA), University College London (GB)
Good health and well-being
Openalex Percentile: Top 19%
Immune cells in cancer
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon