Thrombin contributes to cancer immune evasion via proteolysis of platelet-bound GARP to activate LTGF-β

Alessandra Metelli(Medical University of South Carolina), Bill X. Wu(The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute), Brian Riesenberg(The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute), Silvia Guglietta(Medical University of South Carolina), John D. Huck(Hauptman-Woodward Medical Research Institute), Catherine M. Mills(Medical University of South Carolina), Anqi Li(The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute), Saleh Rachidi(Medical University of South Carolina), Carsten Krieg(Medical University of South Carolina), Mark P. Rubinstein(Medical University of South Carolina), D.T. Gewirth(Hauptman-Woodward Medical Research Institute), Shaoli Sun(Medical University of South Carolina), Michael B. Lilly(Medical University of South Carolina), Amy H. Wahlquist(Medical University of South Carolina), David P. Carbone(The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute), Yiping Yang(The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute), Bei Liu(Medical University of South Carolina), Zihai Li(Medical University of South Carolina)
Science Translational Medicine
January 8, 2020
Cited by 131Open Access
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Abstract

Cancer-associated thrombocytosis and high concentrations of circulating transforming growth factor-β1 (TGF-β1) are frequently observed in patients with progressive cancers. Using genetic and pharmacological approaches, we show a direct link between thrombin catalytic activity and release of mature TGF-β1 from platelets. We found that thrombin cleaves glycoprotein A repetitions predominant (GARP), a cell surface docking receptor for latent TGF-β1 (LTGF-β1) on platelets, resulting in liberation of active TGF-β1 from the GARP-LTGF-β1 complex. Furthermore, systemic inhibition of thrombin obliterates TGF-β1 maturation in platelet releasate and rewires the tumor microenvironment toward favorable antitumor immunity, which translates into efficient cancer control either alone or in combination with programmed cell death 1-based immune checkpoint blockade therapy. Last, we demonstrate that soluble GARP and GARP-LTGF-β1 complex are present in the circulation of patients with cancer. Together, our data reveal a mechanism of cancer immune evasion that involves thrombin-mediated GARP cleavage and the subsequent TGF-β1 release from platelets. We propose that blockade of GARP cleavage is a valuable therapeutic strategy to overcome cancer's resistance to immunotherapy.


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