Cited by 190Monoclonal and Polyclonal Antibodies Researchvaccines and immunoinformatics approachesComputational Drug Discovery Methods

BioPhi: A platform for antibody design, humanization, and humanness evaluation based on natural antibody repertoires and deep learning

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Prihoda, David, Maamary, Jad, Waight, Andrew, Juan, Veronica, Fayadat-Dilman, Laurence, Svozil, Daniel, Bitton, Danny A.·2022·mAbs

Published version of a preprint

Abstract

Abstract Despite recent advances in transgenic animal models and display technologies, humanization of mouse sequences remains the primary route for therapeutic antibody development. Traditionally, humanization is manual, laborious, and requires expert knowledge. Although automation efforts are advancing, existing methods are either demonstrated on a small scale or are entirely proprietary. To predict the immunogenicity risk, the human-likeness of sequences can be evaluated using existing humanness scores, but these lack diversity, granularity or interpretability. Meanwhile, immune repertoire sequencing has generated rich antibody libraries such as the Observed Antibody Space (OAS) that offer augmented diversity not yet exploited for antibody engineering. Here we present BioPhi, an open-source platform featuring novel methods for humanization (Sapiens) and humanness evaluation (OASis). Sapiens is a deep learning humanization method trained on the OAS database using language modeling. Based on an in silico humanization benchmark of 177 antibodies, Sapiens produced sequences at scale while achieving results comparable to that of human experts. OASis is a granular, interpretable and diverse humanness score based on 9-mer peptide search in the OAS. OASis separated human and non-human sequences with high accuracy, and correlated with clinical immunogenicity. Together, BioPhi offers an antibody design interface with automated methods that capture the richness of natural antibody repertoires to produce therapeutics with desired properties and accelerate antibody discovery campaigns. BioPhi is accessible at https://biophi.dichlab.org and https://github.com/Merck/BioPhi .

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References 54 · Cited by 190

Research works printed but not linked: 2

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Authors
Prihoda, D., Maamary, J., Waight, A., Juan, V., Fayadat-Dilman, L., Svozil, D., & Bitton, D. A.
Affiliations
  • Department of Informatics and Chemistry, University of Chemistry and Technology, Prague, Czech Republic
  • Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
  • Discovery Biologics, Protein Sciences, MRL, Merck & Co., Inc, South San Francisco, CA, USA
  • Czech Academy of Sciences, Institute of Molecular Genetics (CZ)
  • MSD (Czech Republic) (CZ)
Corresponding author
Bitton, Danny A.
Venue
mAbs
Published
2022-02-08
Volume
14
Issue
1
Pages
2020203-2020203
ISSN
  • 1942-0862 (ISSN-L)
  • 1942-0870
OpenAlex
W4220757565
Cited by
190
References
54
Citations by year
2026: 36 · 2025: 65 · 2024: 50 · 2023: 28 · 2022: 11
FWCI
21.84
Type
journal article
Language
en
Open access
Locations
  • mAbs (publishedVersion, cc-by-nc)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nd)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA
  • Ministry of Education, Youth and Sports of the Czech Republic (LM2018130)
Topics
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
  • Physical Sciences › Computer Science › Computational Theory and Mathematics › Computational Drug Discovery Methods
Keywords
antibody humanization, therapeutic antibody design, immunogenicity prediction, language modeling, antibody discovery
MeSH terms
Deep Learning, Animals, Antibodies, Mice

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