Abstract LB-C012: Immune-Like Circulating Tumor Cells and Large Extracellular Vesicles in Metastatic Breast Cancer

Abstract Circulating tumor cells (CTCs) provide a minimally invasive window into cancer biology and metastatic progression. However, their phenotypic heterogeneity extends beyond classical epithelial marker expression to include subsets with immune features. Using high-resolution single-cell genomic and proteomic profiling of peripheral blood from patients with stage 4 breast cancer, we identified a distinct population of immune-like CTCs (im.CTCs) that co-express epithelial and immune markers, including CD45, CD3, and CD4. These im.CTCs share clonal, tumor-specific genomic alterations with canonical epithelial CTCs, indicating a non-fusion origin and supporting the existence of a previously unrecognized tumor cell plasticity state. We further observed direct physical interactions between circulating white blood cells, predominantly CD4+ T cells, and both im.CTCs and immune marker–positive large extracellular vesicles (im.LEVs) in patient blood samples. Immune membrane markers were enriched at sites of cell–cell contact, consistent with membrane transfer as a mechanism by which tumor-derived circulating analytes acquire immune features. Together, these findings demonstrate that tumor–immune cell interactions in circulation contribute to the emergence of hybrid phenotypes among circulating tumor analytes. This phenomenon has important implications for liquid biopsy interpretation, immune modulation, and the biology of metastatic dissemination. Future work will be required to define the functional consequences of immune marker expression on CTCs and extracellular vesicles and to determine how these interactions influence immune surveillance, metastatic potential, and clinical outcomes. Citation Format: Stephanie N. Shishido, Peter Kuhn, James Hicks, Nikki Higa, Amin Naghdloo, Mohamed Kamal, Dean Tessone, Valerie Hennes, Audrey Limb, Andres Rivera, Rafael Nevarez, Anand Kolatkar, Carol K. Tweed, Adam I. Riker, Young Lee, Lorraine Tafra, Jeremy Perkins, Craig D. Shriver. Immune-Like Circulating Tumor Cells and Large Extracellular Vesicles in Metastatic Breast Cancer [abstract]. In: Proceedings of the AACR Immuno-Oncology Conference (AACR IO): Discovery and Innovation in Cancer Immunology: Revolutionizing Treatment through Immunotherapy; 2026 Feb 18-21; Los Angeles, CA. Philadelphia (PA): AACR; Cancer Immunol Res 2026;14(2 Suppl):Abstract nr LB-C012.

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Journal
Cancer Immunology Research
Published
2026-03-05
DOI
https://doi.org/10.1158/2326-6074.io2026-lb-c012
Primary Topic
Extracellular vesicles in disease
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article
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article

Abstract LB-C012: Immune-Like Circulating Tumor Cells and Large Extracellular Vesicles in Metastatic Breast Cancer

Rafael Nevarez, Valerie Hennes, Amin Naghdloo, Stephanie N. Shishido et al.
Cancer Immunology Research
Extracellular vesicles in disease
article

Abstract LB-C012: Immune-Like Circulating Tumor Cells and Large Extracellular Vesicles in Metastatic Breast Cancer

Rafael Nevarez, Valerie Hennes, Amin Naghdloo, Stephanie N. Shishido, Lorraine Tafra, Dean Tessone, Nikki Higa, Carol Tweed, Adam I. Riker, Young Joo Lee, Audrey Limb, C. D. Shriver, Anand Kolatkar, Mohamed Kamal, Andres Rivera, Jeremy Perkins, Peter Kuhn, James Hicks
article en

Abstract

Abstract Circulating tumor cells (CTCs) provide a minimally invasive window into cancer biology and metastatic progression. However, their phenotypic heterogeneity extends beyond classical epithelial marker expression to include subsets with immune features. Using high-resolution single-cell genomic and proteomic profiling of peripheral blood from patients with stage 4 breast cancer, we identified a distinct population of immune-like CTCs (im.CTCs) that co-express epithelial and immune markers, including CD45, CD3, and CD4. These im.CTCs share clonal, tumor-specific genomic alterations with canonical epithelial CTCs, indicating a non-fusion origin and supporting the existence of a previously unrecognized tumor cell plasticity state. We further observed direct physical interactions between circulating white blood cells, predominantly CD4+ T cells, and both im.CTCs and immune marker–positive large extracellular vesicles (im.LEVs) in patient blood samples. Immune membrane markers were enriched at sites of cell–cell contact, consistent with membrane transfer as a mechanism by which tumor-derived circulating analytes acquire immune features. Together, these findings demonstrate that tumor–immune cell interactions in circulation contribute to the emergence of hybrid phenotypes among circulating tumor analytes. This phenomenon has important implications for liquid biopsy interpretation, immune modulation, and the biology of metastatic dissemination. Future work will be required to define the functional consequences of immune marker expression on CTCs and extracellular vesicles and to determine how these interactions influence immune surveillance, metastatic potential, and clinical outcomes. Citation Format: Stephanie N. Shishido, Peter Kuhn, James Hicks, Nikki Higa, Amin Naghdloo, Mohamed Kamal, Dean Tessone, Valerie Hennes, Audrey Limb, Andres Rivera, Rafael Nevarez, Anand Kolatkar, Carol K. Tweed, Adam I. Riker, Young Lee, Lorraine Tafra, Jeremy Perkins, Craig D. Shriver. Immune-Like Circulating Tumor Cells and Large Extracellular Vesicles in Metastatic Breast Cancer [abstract]. In: Proceedings of the AACR Immuno-Oncology Conference (AACR IO): Discovery and Innovation in Cancer Immunology: Revolutionizing Treatment through Immunotherapy; 2026 Feb 18-21; Los Angeles, CA. Philadelphia (PA): AACR; Cancer Immunol Res 2026;14(2 Suppl):Abstract nr LB-C012.

Cancer Immunology ResearchVol. 14(2_Supplement)
Uniformed Services University of the Health Sciences (US), Anne Arundel Medical Center (US), Istituto De Angeli (Italy) (IT)
Openalex Percentile: Top 32%
Extracellular vesicles in disease
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