The glycosaminoglycan oncofetal chondroitin sulfate is a novel target for antibody-drug conjugate therapy for AML

Antibody-drug conjugates (ADCs) have emerged as promising targeted therapies for acute myeloid leukemia (AML). However, most ADCs exhibit off-target binding to normal hematopoietic stem and myeloid progenitor cells, resulting in adverse hematotoxicity and narrow therapeutic windows, thereby limiting their clinical application to young and fit patients with AML who are eligible for intensive curative therapies. Proteoglycans with high levels of the glycosaminoglycan oncofetal chondroitin sulfate (ofCS) are abundantly expressed in solid cancers but are absent or expressed at low levels in normal adult tissues. Here, we report high ofCS levels on bone marrow (BM) cells from patients with AML and patient-derived xenografts (PDXs) from these patients, whereas BM cells from healthy individuals showed low or undetectable ofCS levels. Consistently, an anti-ofCS antibody demonstrated binding to and internalization into AML cells, and anti-ofCS ADCs effectively killed AML cells in vitro. Moreover, anti-ofCS ADC treatment significantly prolonged survival of AML PDXs compared with controls and was associated with low toxicity. Thus, anti-ofCS ADCs could represent an effective therapy with acceptable toxicity for patients with AML, including those who are ineligible for or unresponsive to current intensive curative therapies. In conclusion, this study demonstrates, to our knowledge for the first time, that a glycosaminoglycan-like ofCS is a druggable target for the development of effective antibody-based AML therapies.

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Journal
Blood
Published
2025-12-17
DOI
https://doi.org/10.1182/blood.2024028147
Citations
1
Primary Topic
Proteoglycans and glycosaminoglycans research
Type
article
Field-Weighted Citation Impact
1.15
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article

The glycosaminoglycan oncofetal chondroitin sulfate is a novel target for antibody-drug conjugate therapy for AML

Kirsten Grønbæk, Montserrat Estruch, Caroline Løppke, Mette Ø. Agerbæk et al.
1 citations
Blood
Proteoglycans and glycosaminoglycans research
1.15
article

The glycosaminoglycan oncofetal chondroitin sulfate is a novel target for antibody-drug conjugate therapy for AML

Kirsten Grønbæk, Montserrat Estruch, Caroline Løppke, Mette Ø. Agerbæk, Bo Porse, Mie A. Nordmaj, S. Qin, Swati Choudhary, Brigitte Kircher, Yen Nguyen, Olaf T Heidenreich, Robert Dagil, Thor G. Theander, Kim Theilgaard‐Mönch, Elena Ethel Vidal-Calvo, Jan Mueller, Anne Louise Tølbøll Sørensen, Ali Salanti, Joana Mujollari, Priya Khadgawat, Tobias Gustavsson, Norbert Redlinger
article en
1 citations

Abstract

Antibody-drug conjugates (ADCs) have emerged as promising targeted therapies for acute myeloid leukemia (AML). However, most ADCs exhibit off-target binding to normal hematopoietic stem and myeloid progenitor cells, resulting in adverse hematotoxicity and narrow therapeutic windows, thereby limiting their clinical application to young and fit patients with AML who are eligible for intensive curative therapies. Proteoglycans with high levels of the glycosaminoglycan oncofetal chondroitin sulfate (ofCS) are abundantly expressed in solid cancers but are absent or expressed at low levels in normal adult tissues. Here, we report high ofCS levels on bone marrow (BM) cells from patients with AML and patient-derived xenografts (PDXs) from these patients, whereas BM cells from healthy individuals showed low or undetectable ofCS levels. Consistently, an anti-ofCS antibody demonstrated binding to and internalization into AML cells, and anti-ofCS ADCs effectively killed AML cells in vitro. Moreover, anti-ofCS ADC treatment significantly prolonged survival of AML PDXs compared with controls and was associated with low toxicity. Thus, anti-ofCS ADCs could represent an effective therapy with acceptable toxicity for patients with AML, including those who are ineligible for or unresponsive to current intensive curative therapies. In conclusion, this study demonstrates, to our knowledge for the first time, that a glycosaminoglycan-like ofCS is a druggable target for the development of effective antibody-based AML therapies.

BloodVol. 147(11)
University of Copenhagen (DK), Innsbruck Medical University (AT), University of Southern Denmark (DK), Copenhagen Business School (DK), Universität Innsbruck (AT), Frederiksberg Hospital (DK), Odense University Hospital (DK), Copenhagen University Hospital (DK), Rigshospitalet (DK), Princess Máxima Center (NL), Capital Region of Denmark (DK), IT University of Copenhagen (DK), Newcastle University (GB)
Openalex Percentile: Top 17%
Proteoglycans and glycosaminoglycans research
1.15
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