Evidence map›Paper›PMID 41717447›Full record

ArticleFrontiers in immunology2025

Enhancing Named Entity Recognition for immunology and immune-mediated disorders.

Songyue Chen, Jinshan Che, Mingming Sun, Yuhong Wang

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Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Songyue ChenDepartment of Rheumatology and Immunology, First Affiliated Hospital of Bengbu Medical University, Bengbu, China.
Jinshan CheFourth Clinical College of Xinxiang Medical College, Xinxiang Central Hospital, Xinxiang, China.
Mingming SunFourth Clinical College of Xinxiang Medical College, Xinxiang Central Hospital, Xinxiang, China.
Yuhong WangFourth Clinical College of Xinxiang Medical College, Xinxiang Central Hospital, Xinxiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Named Entity Recognition (NER) in the biomedical domain, particularly within immunology and immune-mediated disorders, presents unique challenges due to the presence of complex, nested, and overlapping entities. Existing NER systems often struggle with the specialized terminologies and contextual ambiguity of immunological texts, which limits their effectiveness in downstream biomedical applications. Methods: To address these challenges, we propose a domain-specific NERframework that integrates structured span encoding and knowledge-guided decoding. The framework is designed to enhance recognition accuracy under low-resource and weak supervision conditions by combining a hierarchical span encoder (SpanStructEncoder) with a constraint-based decoding strategy (Contextual Constraint Decoding, CCD). We evaluate our model on three immunology-specific datasets: the NCBI Disease Corpus (immune-related diseases), SNPPhenA (genetic variants and phenotype associations), and HLA-SPREAD (HLA-disease and drug-response relations). These datasets were selected because they represent key immunological concepts such as cytokines, immune cell types, and genetic markers that underlie immune responses and disease mechanisms. Results and discussion: Experimental results demonstrate that our model achieves consistent improvements in F1-score over strong biomedical baselines including BioGPT, BioLinkBERT, and SciFive. Our results confirm that incorporating structured span representations and ontology-aware decoding significantly improves entity extraction for immunology-related texts. The proposed framework provides a robust and interpretable solution for immunology-focused biomedical text mining, facilitating applications in literature curation, biomarker discovery, and clinical decision support.

Indexed as

Allergy and ImmunologyData MiningImmune System DiseasesHumansImmunoinformaticsTerminology as Topicbiomedical NLPconstraint-based decodingimmunologynamed entity recognitionstructural span encoding

Identifiers

PMID41717447
PMCPMC12913371

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.