Epitope specific antibodies and T cell receptors in the immune epitope database
Open accessAbstract
The Immune Epitope Database (IEDB) is a free public resource which catalogs experiments characterizing immune epitopes. To accommodate data from next generation repertoire sequencing experiments, we recently updated how we capture and query epitope specific antibodies and T cell receptors. Specifically, we are now storing partial receptor sequences sufficient to determine CDRs and VDJ gene usage which are commonly identified by repertoire sequencing. For previously captured full length receptor sequencing data, we have calculated the corresponding CDR sequences and gene usage information using IMGT numbering and VDJ gene nomenclature format. To integrate information from receptors defined at different levels of resolution, we grouped receptors based on their host species, receptor type and CDR3 sequence. As of August 2018, we have cataloged sequence information for more than 22,510 receptors in 18,292 receptor groups, shown to bind to more than 2,241 distinct epitopes. These data are accessible as full exports and through a new dedicated query interface. The later combines the new ability to search by receptor characteristics with previously existing capability to search by epitope characteristics such as the infectious agent the epitope is derived from, or the kind of immune response involved in its recognition. We expect that this comprehensive capture of epitope specific immune receptor information will provide new insights into receptor-epitope interactions, and facilitate the development of novel tools that help in the analysis of receptor repertoire data.
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Data on epitopes targeted by antibodies can be readily downloaded from the IEDB that now links such information to epitope-specific antibody sequences.
“Data on epitopes targeted by antibodies can be readily downloaded from the IEDB that now links such information to epitope-specific antibody sequences [67].”
From Computational approaches to therapeutic antibody design: established methods and emerging trends (2020) · cites this paper as [67]
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References 35 · Cited by 53
- Authors
- Mahajan, S., Vita, R., Shackelford, D., Lane, J., Schulten, V., Zarebski, L., Jespersen, M. C., Marcatili, P., Nielsen, M., Sette, A., & Peters, B.
- Affiliations
- La Jolla Institute for Immunology (US)
- Technical University of Denmark (DK)
- National University of General San Martín (AR)
- Corresponding author
- Peters, Bjoern
- Venue
- Frontiers in Immunology
- Publisher
- Frontiers Media SA
- Published
- 2018-11-20
- Volume
- 9
- Pages
- 2688-2688
- ISSN
- 1664-3224 (ISSN-L)
- PMC
- PMC6255941
- OpenAlex
- W2901096054
- Cited by
- 53
- References
- 35
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 9 · 2023: 7 · 2022: 8 · 2021: 5 · 2020: 7 · 2019: 7
- FWCI
- 1.69
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Immunology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Technical University of Denmark, DTU Orbit (Technical University of Denmark, DTU) (submittedVersion, other-oa)
- Funders
- National Institutes of Health (HHSN272201200010C)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Keywords
- IEDB, epitope-specific antibodies, T cell receptor, CDR3 sequences, database query interface, immune epitopes
- MeSH terms
- Animals, Antibodies, Antibody Specificity, Humans, Receptors, Antigen, T-Cell, Epitopes, T-Lymphocyte, Databases, Protein, Mice
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