# Improving Antibody Humanness Prediction using Patent Data

arXiv: https://arxiv.org/abs/2401.14442 · HTML: https://mlsanity.com/paper/2401.14442/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 15 of its 34 references that are in the map.
- First posted on arXiv 25 Jan 2024.

## Builds on (most cited first, 15 of 15)

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- [Unsupervised Cross-lingual Representation Learning at Scale](https://mlsanity.com/paper/1911.02116/) (2019)
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- [Bag of Tricks for Efficient Text Classification](https://mlsanity.com/paper/1607.01759/) (2016)
- [SubTab: Subsetting Features of Tabular Data for Self-Supervised Representation Learning](https://mlsanity.com/paper/2110.04361/) (2021)
- [Deciphering antibody affinity maturation with language models and weakly supervised learning](https://mlsanity.com/paper/2112.07782/) (2021)
- [A Framework For Contrastive Self-Supervised Learning And Designing A New Approach](https://mlsanity.com/paper/2009.00104/) (2020)

## Abstract (arXiv)

We investigate the potential of patent data for improving the antibody humanness prediction using a multi-stage, multi-loss training process. Humanness serves as a proxy for the immunogenic response to antibody therapeutics, one of the major causes of attrition in drug discovery and a challenging obstacle for their use in clinical settings. We pose the initial learning stage as a weakly-supervised contrastive-learning problem, where each antibody sequence is associated with possibly multiple identifiers of function and the objective is to learn an encoder that groups them according to their patented properties. We then freeze a part of the contrastive encoder and continue training it on the patent data using the cross-entropy loss to predict the humanness score of a given antibody sequence. We illustrate the utility of the patent data and our approach by performing inference on three different immunogenicity datasets, unseen during training. Our empirical results demonstrate that the learned model consistently outperforms the alternative baselines and establishes new state-of-the-art on five out of six inference tasks, irrespective of the used metric.
