PO.BCS01.04 · 生物信息与计算
CEDAR:一个精选的癌症表位和受体综合数据库
CEDAR: A comprehensive database of curated cancer epitopes and receptors
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
识别具有免疫原性的癌症表位,包括患者特异性新表位和共有肿瘤相关抗原(TAA),是推进有效癌症免疫治疗的关键基础。为向学界提供该研究的集中数据源,癌症表位数据库与分析资源(CEDAR,cedar.iedb.org)提供了最广泛且持续更新的经实验验证的癌症表位和受体数据集合。目前,CEDAR收录了来自6,242篇出版物的数据,涵盖152,636项T细胞检测、143,715项B细胞检测和4,394,087项MHC配体检测,覆盖666种不同的限制性MHC等位基因。
CEDAR的综合目录包括新表位、致癌病毒表位和TAA,存储了人类、小鼠及其他物种的阳性和阴性免疫反应。数据库的核心要素是验证这些肿瘤分子相互作用的实验数据;检测信息经过细致报告,包括用于确认T细胞、B细胞和MHC结合/呈递的具体检测类型(如ELISpot、四聚体染色、质谱)。此外,数据库还存储了已知能特异性识别这些表位的T细胞和B细胞受体。
CEDAR的优势在于其严格且透明的精选过程。所有条目均由博士级科学家依据公开可用的精选手册进行精选,该手册概述了数据提取、验证和注释的具体、一致应用的规则。精选人员使用经广泛验证的工作流,将自动化文本挖掘与详细的人工审核相结合,以确保完整性和准确性。数据以高度结构化的方式进行注释,使用社区支持的本体,如Uniprot、疾病本体(Disease Ontology)和生物医学研究本体(OBI)等。这种高度标准化确保了数据准确性,最大化了互操作性,并使用户能够执行高度精细的查询,按物种、MHC分子、癌症病理、抗原类型和特定来源抗原进行筛选。
作为免疫表位数据库(IEDB)不可或缺且免费访问的配套网站,CEDAR是基础和转化免疫肿瘤学研究的关键基础。它提供了验证预测模型、设计靶向治疗和探索肿瘤免疫图景所必需的高质量、可信的实验数据。
查看英文原文 English abstract
The identification of immunogenic cancer epitopes, including patient-specific neoepitopes and shared tumor-associated antigens (TAAs), is a critical foundation for advancing effective cancer immunotherapies. To provide the community with a centralized data source for this research, the Cancer Epitope Database and Analysis Resource (CEDAR, cedar.iedb.org) offers the most extensive and actively updated collection of experimentally validated cancer epitope and receptor data. Currently, CEDAR hosts data from 6,242 publications, encompassing 152,636 T Cell Assays, 143,715 B Cell Assays, and 4,394,087 MHC Ligand Assays, covering 666 distinct restricting MHC alleles.
CEDAR's comprehensive catalog includes neoepitopes, oncoviral epitopes, and TAAs, storing both positive and negative immune responses across human, mouse, and other species. The central element of the database is the experimental data validating these tumor molecule interactions; assay information is meticulously reported, including the specific assay types (e.g., ELISpot, tetramer staining, mass spectrometry) used to confirm T cell, B cell, and MHC binding/presentation. Furthermore, the database stores T and B cell receptors known to specifically recognize these epitopes.
The strength of the CEDAR lies in its rigorous and transparent curation process. All entries are curated by PhD-level scientists following a publicly available curation manual that outlines specific, consistently applied rules for data extraction, validation, and annotation. Curators use extensively validated workflows that combine automated text-mining with detailed manual review to ensure completeness and accuracy. Data is annotated in a highly structured way using community-supported ontologies, such as Uniprot, the Disease Ontology, and The Ontology for Biomedical Investigations (OBI), among others. This high degree of standardization ensures data accuracy, maximizes interoperability, and enables users to perform highly granular queries, filtering by species, MHC molecules, cancer pathology, antigen type, and specific source antigens.
As an integral and freely accessible companion site to the Immune Epitope Database (IEDB), CEDAR serves as a critical foundation for basic and translational immuno-oncology research. It provides the high-quality, trusted experimental data necessary for validating predictive models, designing targeted therapeutics, and exploring the landscape of tumor immunity.
利益披露 Disclosure
Z. Kosaloglu-Yalcin, None..
I. Carri, None..
N. Blazeska, None..
R. Vita, None..
D. Marrama, None..
M. Nielsen, None..
A. Sette, None.
B. Peters,
Amgen Other, Speaker, consultant.
Sanofi Other, Speaker, consultant.