Abstract A026: Discovery and development of a transferrin receptor antibody panel for efficient blood-brain barrier delivery as part of a multispecific antibody

Abstract Therapeutic delivery across the blood-brain barrier (BBB) remains a significant challenge in developing treatments for neurological diseases, particularly for protein-based therapeutics. One promising delivery approach utilizes receptor-mediated transcytosis (RMT). In this approach, therapeutics are targeted to a receptor present in the brain endothelia, typically via a secondary binding domain, which facilitates transport of the bound therapeutic. Transferrin receptor (TfR) and CD98 heavy chain (CD98HC) are two receptors that are attractive targets for this receptor-targeted BBB delivery. TfR has been a primary focus due to its well-characterized transport properties. Using a yeast-based antibody discovery platform, we have discovered and optimized a diverse panel of conventional (IgG) and single-domain antibodies (sdAbs) that target TfR. These antibodies show a range of binding affinities to TfR and do not compete with endogenous transferrin binding. The panel displays diverse epitope breadth and cross-reactivity between human and cynomolgus TfR. The panel exhibits rapid internalization in TfR-expressing Jurkat cells and in a brain endothelial cell line (hCMEC/D3). Finally, we have generated a panel of 2+1 multispecific antibodies containing two anti-BACE1 Fab arms and a C-terminal fusion of the anti-TfR binder (Fab or sdAb) for in vivo BBB permeability assessment using a humanized mouse TfR model. The 2+1 multispecifics showed improved uptake across the BBB compared to an anti-BACE1 antibody containing a non-TfR-binding C-terminal Fab. The TfR antibody panel developed here provides a novel toolset to aid in the development of complex multispecific antibodies across neurological indications. Citation Format: Nadthakarn Boland, Emma Cammack, Olivia Scheideler, John Martel, Robert Pejchal, Eric Krauland, Emily Radke, Kevin Schutz, Bradley M. Lunde. Discovery and development of a transferrin receptor antibody panel for efficient blood-brain barrier delivery as part of a multispecific antibody [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Brain Cancer; 2026 Mar 23-25; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(6_Suppl):Abstract nr A026.

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Journal
Cancer Research
Published
2026-03-23
DOI
https://doi.org/10.1158/1538-7445.brain26-a026
Primary Topic
Barrier Structure and Function Studies
Type
article
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article

Abstract A026: Discovery and development of a transferrin receptor antibody panel for efficient blood-brain barrier delivery as part of a multispecific antibody

Kevin Schutz, Nadthakarn Boland, Olivia J. Scheideler, Eric Krauland et al.
Cancer Research
Barrier Structure and Function Studies
article

Abstract A026: Discovery and development of a transferrin receptor antibody panel for efficient blood-brain barrier delivery as part of a multispecific antibody

Kevin Schutz, Nadthakarn Boland, Olivia J. Scheideler, Eric Krauland, Emily E. Radke, Bradley Lunde, Robert Pejchal, Emma Cammack, John Martel
article en

Abstract

Abstract Therapeutic delivery across the blood-brain barrier (BBB) remains a significant challenge in developing treatments for neurological diseases, particularly for protein-based therapeutics. One promising delivery approach utilizes receptor-mediated transcytosis (RMT). In this approach, therapeutics are targeted to a receptor present in the brain endothelia, typically via a secondary binding domain, which facilitates transport of the bound therapeutic. Transferrin receptor (TfR) and CD98 heavy chain (CD98HC) are two receptors that are attractive targets for this receptor-targeted BBB delivery. TfR has been a primary focus due to its well-characterized transport properties. Using a yeast-based antibody discovery platform, we have discovered and optimized a diverse panel of conventional (IgG) and single-domain antibodies (sdAbs) that target TfR. These antibodies show a range of binding affinities to TfR and do not compete with endogenous transferrin binding. The panel displays diverse epitope breadth and cross-reactivity between human and cynomolgus TfR. The panel exhibits rapid internalization in TfR-expressing Jurkat cells and in a brain endothelial cell line (hCMEC/D3). Finally, we have generated a panel of 2+1 multispecific antibodies containing two anti-BACE1 Fab arms and a C-terminal fusion of the anti-TfR binder (Fab or sdAb) for in vivo BBB permeability assessment using a humanized mouse TfR model. The 2+1 multispecifics showed improved uptake across the BBB compared to an anti-BACE1 antibody containing a non-TfR-binding C-terminal Fab. The TfR antibody panel developed here provides a novel toolset to aid in the development of complex multispecific antibodies across neurological indications. Citation Format: Nadthakarn Boland, Emma Cammack, Olivia Scheideler, John Martel, Robert Pejchal, Eric Krauland, Emily Radke, Kevin Schutz, Bradley M. Lunde. Discovery and development of a transferrin receptor antibody panel for efficient blood-brain barrier delivery as part of a multispecific antibody [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Brain Cancer; 2026 Mar 23-25; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(6_Suppl):Abstract nr A026.

Cancer ResearchVol. 86(6_Supplement)
Adimab (United States) (US)
Openalex Percentile: Top 29%
Barrier Structure and Function Studies
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