Humatch - fast, gene-specific joint humanisation of antibody heavy and light chains

Antibodies are a popular and powerful class of therapeutic due to their ability to exhibit high affinity and specificity to target proteins. However, the majority of antibody therapeutics are not genetically human, with initial therapeutic designs typically obtained from animal models. Humanization of these precursors is essential to reduce immunogenic risks when administered to humans.Here, we present Humatch, a computational tool designed to offer experimental-like joint humanization of heavy and light chains in seconds. Humatch consists of three lightweight Convolutional Neural Networks (CNNs) trained to identify human heavy V-genes, light V-genes, and well-paired antibody sequences with near-perfect accuracy. We show that these CNNs, alongside germline similarity, can be used for fast humanization that aligns well with known experimental data. Throughout the humanization process, a sequence is guided toward a specific target gene and away from others via multiclass CNN outputs and gene-specific germline data. This guidance ensures final humanized designs do not sit 'between' genes, a trait that is not naturally observed. Humatch's optimization toward specific genes and good VH/VL pairing increases the chances that final designs will be stable and express well and reduces the chances of immunogenic epitopes forming between the two chains. Humatch's training data and source code are provided open-source.

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Publication Details

Journal
mAbs
Published
2024-11-29
DOI
https://doi.org/10.1080/19420862.2024.2434121
Citations
9
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
3.64

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article

Humatch - fast, gene-specific joint humanisation of antibody heavy and light chains

Lewis Chinery, Charlotte M. Deane, Jeliazko R. Jeliazkov
9 citations
mAbs
Monoclonal and Polyclonal Antibodies Research
3.64
article

Humatch - fast, gene-specific joint humanisation of antibody heavy and light chains

Lewis Chinery, Charlotte M. Deane, Jeliazko R. Jeliazkov
article en
9 citations

Abstract

Antibodies are a popular and powerful class of therapeutic due to their ability to exhibit high affinity and specificity to target proteins. However, the majority of antibody therapeutics are not genetically human, with initial therapeutic designs typically obtained from animal models. Humanization of these precursors is essential to reduce immunogenic risks when administered to humans.Here, we present Humatch, a computational tool designed to offer experimental-like joint humanization of heavy and light chains in seconds. Humatch consists of three lightweight Convolutional Neural Networks (CNNs) trained to identify human heavy V-genes, light V-genes, and well-paired antibody sequences with near-perfect accuracy. We show that these CNNs, alongside germline similarity, can be used for fast humanization that aligns well with known experimental data. Throughout the humanization process, a sequence is guided toward a specific target gene and away from others via multiclass CNN outputs and gene-specific germline data. This guidance ensures final humanized designs do not sit 'between' genes, a trait that is not naturally observed. Humatch's optimization toward specific genes and good VH/VL pairing increases the chances that final designs will be stable and express well and reduces the chances of immunogenic epitopes forming between the two chains. Humatch's training data and source code are provided open-source.

mAbsVol. 16(1)
Providence College (US), University of Oxford (GB), Applied Technologies (United States) (US)
GlaxoSmithKline, Directorate for Biological Sciences, Biotechnology and Biological Sciences Research Council
Openalex Percentile: Top 6%
Monoclonal and Polyclonal Antibodies Research
3.64
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Humatch - fast, gene-specific joint humanisation of antibody heavy and light chains — Lewis Chinery, Charlotte M. Deane, et al. · mAbs (2024) | TGRS Research Map | TGRS