Investigating the complex interplay between fibroblast activation protein α-positive cancer associated fibroblasts and the tumor microenvironment in the context of cancer immunotherapy

被引:1
|
作者
Kraxner, Anton [1 ]
Braun, Franziska [2 ]
Cheng, Wei-Yi [3 ]
Yang, Tai-Hsien Ou [3 ]
Pipaliya, Shweta [4 ]
Canamero, Marta [5 ]
Andersson, Emilia [5 ]
Harring, Suzana Vega [5 ]
Dziadek, Sebastian [1 ]
Broeske, Ann-Marie E. [5 ]
Ceppi, Maurizio [1 ]
Tanos, Tamara [1 ]
Teichgraber, Volker [1 ]
Charo, Jehad [6 ]
机构
[1] F Hoffmann La Roche Ltd, Roche Innovat Ctr Basel, Roche Pharm Res & Early Dev Oncol, Basel, Switzerland
[2] Roche Diagnost GmbH, Roche Innovat Ctr Munich, Roche Pharm Res & Early Dev Data & Analyt, Penzberg, Germany
[3] F Hoffmann La Roche Ltd, Roche Translat & Clin Res Ctr, Roche Pharm Res & Early Dev Data & Analyt, Little Falls, NJ USA
[4] Roche Glycart AG, Roche Innovat Ctr Zurich, Roche Pharm Res & Early Dev Data & Analyt, Schlieren, Switzerland
[5] Roche Diagnost GmbH, Roche Innovat Ctr Munich, Roche Pharm Res & Early Dev Oncol, Penzberg, Germany
[6] Roche Glycart AG, Roche Innovat Ctr Zurich, Roche Pharm Res & Early Dev, Oncol, Schlieren, Switzerland
来源
FRONTIERS IN IMMUNOLOGY | 2024年 / 15卷
关键词
fibroblast activation protein (FAP); tumor immune microenvironment; T cell infiltration; immune cell subsets; cancer immuno-therapy; patient enrichment; STROMAL FIBROBLASTS; SERINE-PROTEASE; T-CELLS; IMMUNITY; GELATINASE; CARCINOMA; BLOCKADE; GROWTH; IL-10;
D O I
10.3389/fimmu.2024.1352632
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction This study investigates the role of Fibroblast Activation Protein (FAP)-positive cancer-associated fibroblasts (FAP+CAF) in shaping the tumor immune microenvironment, focusing on its association with immune cell functionality and cytokine expression patterns.Methods Utilizing immunohistochemistry, we observed elevated FAP+CAF density in metastatic versus primary renal cell carcinoma (RCC) tumors, with higher FAP+CAF correlating with increased T cell infiltration in RCC, a unique phenomenon illustrating the complex interplay between tumor progression, FAP+CAF density, and immune response.Results Analysis of immune cell subsets in FAP+CAF-rich stromal areas further revealed significant correlations between FAP+ stroma and various T cell types, particularly in RCC and non-small cell lung cancer (NSCLC). This was complemented by transcriptomic analyses, expanding the range of stromal and immune cell subsets interrogated, as well as to additional tumor types. This enabled evaluating the association of these subsets with tumor infiltration, tumor vascularization and other components of the tumor microenvironment. Our comprehensive study also encompassed cytokine, angiogenesis, and inflammation gene signatures across different cancer types, revealing heterogeneous cellular composition, cytokine expressions and angiogenic profiles. Through cytokine pathway profiling, we explored the relationship between FAP+CAF density and immune cell states, uncovering potential immunosuppressive circuits that limit anti-tumor activity in tumor-resident immune cells.Conclusions These findings underscore the complexity of tumor biology and the necessity for personalized therapeutic and patient enrichment approaches. The insights gathered from FAP+CAF prevalence, immune infiltration, and gene signatures provide valuable perspectives on tumor microenvironments, aiding in future research and clinical strategy development.
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页数:13
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