Josua StadelmaierUniversity of Tübingen, Brandon MaloneNEC OncoImmunity, Ralf EggelingUniversity of Tübingen
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引用次数: 0
Abstract
We study the prediction of T-cell response for specific given peptides, which
could, among other applications, be a crucial step towards the development of
personalized cancer vaccines. It is a challenging task due to limited,
heterogeneous training data featuring a multi-domain structure; such data
entail the danger of shortcut learning, where models learn general
characteristics of peptide sources, such as the source organism, rather than
specific peptide characteristics associated with T-cell response. Using a transformer model for T-cell response prediction, we show that the
danger of inflated predictive performance is not merely theoretical but occurs
in practice. Consequently, we propose a domain-aware evaluation scheme. We then
study different transfer learning techniques to deal with the multi-domain
structure and shortcut learning. We demonstrate a per-source fine tuning
approach to be effective across a wide range of peptide sources and further
show that our final model outperforms existing state-of-the-art approaches for
predicting T-cell responses for human peptides.
我们研究了针对特定多肽的 T 细胞反应预测,除其他应用外,这可能是开发个性化癌症疫苗的关键一步。由于具有多域结构的异构训练数据有限,这是一项具有挑战性的任务;此类数据存在捷径学习的危险,即模型学习的是肽源的一般特征,如源生物,而不是与 T 细胞反应相关的特定肽特征。通过使用 T 细胞反应预测的转换器模型,我们发现预测性能膨胀的危险不仅存在于理论上,而且在实践中也时有发生。因此,我们提出了一种领域感知评估方案。然后,我们研究了不同的迁移学习技术,以处理多领域结构和捷径学习。我们证明了按来源进行微调的方法在广泛的肽来源中是有效的,并进一步证明了我们的最终模型在预测人类肽的 T 细胞反应方面优于现有的最先进方法。