DoggifAI: A transformer based approach for antibody caninisation

<h2>Abstract</h2> Antibody translation across species offers a compelling strategy to extend the vast and expensive investments in human therapeutic antibodies to veterinary oncology, with applications in both veterinary medicine and comparative oncology. While precise, low-immunogenic treatments are essential for canine cancer care, traditional species conversion methods rely on ad hoc bioinformatics modifications. These methods often implicitly decouple the framework (FR) and complementarity-determining regions (CDRs), ignoring how structural changes in FRs can affect the conformation and function of CDRs. This can compromise binding specificity and require costly high-throughput <i>in vitro</i> screening. To address this, we present DoggifAI, a transformer model that translates non-canine antibody sequences into canine ones by generating species-appropriate framework regions (FRs) based on desired CDRs. This allows the model to better preserve structural compatibility between FRs and CDRs. The model is pretrained in a T5-style text-to-text denoising task on a large multispecies antibody dataset, which allows further finetuning on a much smaller species-specific dataset. DoggifAI generates highly canine-like antibodies and shows promising results in preserving binding specificity. To support further progress in this field, we also release a curated dataset of over 430,000 unique canine antibody chain sequences, significantly expanding the public sequence repertoire.

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Publication Details

Journal
ImmunoInformatics
Published
2025-11-08
DOI
https://doi.org/10.1016/j.immuno.2025.100064
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00

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article

DoggifAI: A transformer based approach for antibody caninisation

Javier A. Alfaro, Maciej Parys, Mikołaj Kocikowski, Shay B. Cohen et al.
ImmunoInformatics
Monoclonal and Polyclonal Antibodies Research
article

DoggifAI: A transformer based approach for antibody caninisation

Javier A. Alfaro, Maciej Parys, Mikołaj Kocikowski, Shay B. Cohen, Douglas R. Houston, Ted R. Hupp, Dominik Grabarczyk
article en

Abstract

<h2>Abstract</h2> Antibody translation across species offers a compelling strategy to extend the vast and expensive investments in human therapeutic antibodies to veterinary oncology, with applications in both veterinary medicine and comparative oncology. While precise, low-immunogenic treatments are essential for canine cancer care, traditional species conversion methods rely on ad hoc bioinformatics modifications. These methods often implicitly decouple the framework (FR) and complementarity-determining regions (CDRs), ignoring how structural changes in FRs can affect the conformation and function of CDRs. This can compromise binding specificity and require costly high-throughput <i>in vitro</i> screening. To address this, we present DoggifAI, a transformer model that translates non-canine antibody sequences into canine ones by generating species-appropriate framework regions (FRs) based on desired CDRs. This allows the model to better preserve structural compatibility between FRs and CDRs. The model is pretrained in a T5-style text-to-text denoising task on a large multispecies antibody dataset, which allows further finetuning on a much smaller species-specific dataset. DoggifAI generates highly canine-like antibodies and shows promising results in preserving binding specificity. To support further progress in this field, we also release a curated dataset of over 430,000 unique canine antibody chain sequences, significantly expanding the public sequence repertoire.

ImmunoInformaticsVol. 20
Roslin Institute (GB), University of Calgary (CA), Edinburgh Cancer Research (GB), University of Gdańsk (PL), Institute of Genetics and Cancer (GB), University of Edinburgh (GB)
Israel Cancer Research Fund, UK Research and Innovation, Royal Academy of Engineering, University of Bristol
Openalex Percentile: Top 52%
Monoclonal and Polyclonal Antibodies Research
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