Abstract 4800: Targeting CD160 as an immunotherapy approach to modulate tumor angiogenesis and improve outcomes in triple-negative breast cancer

Abstract Triple-negative breast cancer (TNBC) is an aggressive subtype with limited treatment options and poor clinical outcomes. While immune checkpoint inhibitors (ICIs) have shown promise in TNBC, many patients remain unresponsive, highlighting the urgent need for new immunotherapeutic targets and mechanisms. CD160, a GPI-anchored receptor expressed on cytotoxic immune and endothelial cells, we have recently been proposed CD160 as a novel immune checkpoint inhibitor in solid tumors (Scheffges, Devy, et al. 2024). In this study, we investigated CD160 as a dual therapeutic target in TNBC, combining immunoregulatory and anti-angiogenic potential. Using a novel high-affinity monoclonal antibody against CD160, we demonstrate that targeting this receptor significantly inhibits pathological angiogenesis and promotes vascular normalization in vitro and ex vivo, without inducing cytotoxicity. These effects may contribute to enhanced immune infiltration and improved tumor perfusion, ultimately improving patient survival. To better understand CD160’s mechanism of action, we explored its molecular interactions in human endothelial cells. Super-resolution microscopy and functional assays revealed that CD160 physically associates with LRP1, identifying it as a potential co-receptor involved in its vascular effects. These findings support the development of CD160-targeted immunotherapy as a promising strategy for TNBC, acting both as an immune checkpoint inhibitor and a modulator of the tumor vasculature. References : Scheffges C, Devy J, Giustiniani J, Francois S, Cartier L, Merrouche Y, Foussat A, Potteaux S, Bensussan A, Marie-Cardine A. Identification of CD160-TM as a tumor target on triple negative breast cancers: possible therapeutic applications. Breast Cancer Res. 2024 Feb 15;26(1):28. doi: 10.1186/s13058-024-01785-x. PMID: 38360636; PMCID: PMC10870674. Citation Format: Abdel-Ilah Aziz, Maxence Mocquery-Corre, Chloé Jean, Jessica Thevenard-Devy, Alexandre Berquand, Sabrina Haddou, Cathy Hachet, André F. Martins, Rachid El fatimy, Laurent Duca, Armand Bensussan, Sanae Ben Mkaddem, Jérôme Devy. Targeting CD160 as an immunotherapy approach to modulate tumor angiogenesis and improve outcomes in triple-negative breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4800.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-4800
Primary Topic
Nanoplatforms for cancer theranostics
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article
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article

Abstract 4800: Targeting CD160 as an immunotherapy approach to modulate tumor angiogenesis and improve outcomes in triple-negative breast cancer

Sanae Ben Mkaddem, C Hachet, Abdel-ilah Aziz, Jessica Thevenard-Devy et al.
Cancer Research
Nanoplatforms for cancer theranostics
article

Abstract 4800: Targeting CD160 as an immunotherapy approach to modulate tumor angiogenesis and improve outcomes in triple-negative breast cancer

Sanae Ben Mkaddem, C Hachet, Abdel-ilah Aziz, Jessica Thevenard-Devy, André F. Martins, Alexandre Berquand, Armand Bensussan, Laurent Duca, Jérôme Devy, Sabrina Haddou, Rachid Elfatimy, C. Manson Jean, Maxence Mocquery-Corre
article en

Abstract

Abstract Triple-negative breast cancer (TNBC) is an aggressive subtype with limited treatment options and poor clinical outcomes. While immune checkpoint inhibitors (ICIs) have shown promise in TNBC, many patients remain unresponsive, highlighting the urgent need for new immunotherapeutic targets and mechanisms. CD160, a GPI-anchored receptor expressed on cytotoxic immune and endothelial cells, we have recently been proposed CD160 as a novel immune checkpoint inhibitor in solid tumors (Scheffges, Devy, et al. 2024). In this study, we investigated CD160 as a dual therapeutic target in TNBC, combining immunoregulatory and anti-angiogenic potential. Using a novel high-affinity monoclonal antibody against CD160, we demonstrate that targeting this receptor significantly inhibits pathological angiogenesis and promotes vascular normalization in vitro and ex vivo, without inducing cytotoxicity. These effects may contribute to enhanced immune infiltration and improved tumor perfusion, ultimately improving patient survival. To better understand CD160’s mechanism of action, we explored its molecular interactions in human endothelial cells. Super-resolution microscopy and functional assays revealed that CD160 physically associates with LRP1, identifying it as a potential co-receptor involved in its vascular effects. These findings support the development of CD160-targeted immunotherapy as a promising strategy for TNBC, acting both as an immune checkpoint inhibitor and a modulator of the tumor vasculature. References : Scheffges C, Devy J, Giustiniani J, Francois S, Cartier L, Merrouche Y, Foussat A, Potteaux S, Bensussan A, Marie-Cardine A. Identification of CD160-TM as a tumor target on triple negative breast cancers: possible therapeutic applications. Breast Cancer Res. 2024 Feb 15;26(1):28. doi: 10.1186/s13058-024-01785-x. PMID: 38360636; PMCID: PMC10870674. Citation Format: Abdel-Ilah Aziz, Maxence Mocquery-Corre, Chloé Jean, Jessica Thevenard-Devy, Alexandre Berquand, Sabrina Haddou, Cathy Hachet, André F. Martins, Rachid El fatimy, Laurent Duca, Armand Bensussan, Sanae Ben Mkaddem, Jérôme Devy. Targeting CD160 as an immunotherapy approach to modulate tumor angiogenesis and improve outcomes in triple-negative breast cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 4800.

Cancer ResearchVol. 86(7_Supplement)
Centre National de la Recherche Scientifique (FR), Siemens (Germany) (DE), Université Mohammed VI Polytechnique (MA), Université de Reims Champagne-Ardenne (FR)
Openalex Percentile: Top 33%
Nanoplatforms for cancer theranostics
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