Abstract
Background: The identification of B-cell epitopes, the regions that bind to antibodies, is essential for creating effective prophylactic treatments against infectious diseases and cancer, particularly in the realm of reverse vaccinology. While experimental techniques like X-ray crystallography and peptide arrays help identify epitopes, they are expensive, time-consuming and differ in throughput and precision. Methods: This review examines how predictive techniques and datasets have evolved for the problem, highlighting recent breakthroughs in data-driven algorithms used to predict B-cell epitopes. We specifically examine how methodologies have progressed from traditional machine learning to cutting-edge deep learning models. Conclsion: The review summarizes significant research contributions in this domain including linear and conformational epitope prediction techniques, addresses methodological biases, dataset limitations, systematic evaluation challenges that plague the field, and explores future opportunities for innovation.
| Original language | English |
|---|---|
| Article number | 248 |
| Journal | Journal of Translational Medicine |
| Volume | 24 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Dec 2026 |
Keywords
- B-cell epitopes
- Linear conformational epitopes
- Machine learning
- Protein Language Models (PLMs)
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