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March 5, 2026Biomedicines0 citationsOpen Access

TCR Repertoire Analysis Unveils the Link Between Kawasaki Disease and Viral Infection

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ZGZhimi GengWZWei ZhouZFZhihao Fang

Key Points

  • This study aims to investigate the connection between Kawasaki disease and viral infections through TCR repertoire analysis.
  • Compared TCR repertoires from KD patients, healthy controls, and individuals with viral infections.
  • Assessed TCR diversity and V(D)J usage using Shannon’s entropy and statistical tests.
  • Conducted positional motif enrichment analysis within CDR3 regions to identify paratope hotspots.
  • KD patients had reduced TCR clonal abundance and diversity compared to healthy controls.
  • Overlap in VJ gene segment usage was significant between KD and cytomegalovirus infection.
  • A prominent TCR combination with specific amino acid motifs was frequently found in KD.

Abstract

Background: Kawasaki disease (KD) is a systemic vasculitis of unknown origin, though recent evidence implicates viral pathogens in its pathogenesis. Given the central role of T cell receptors (TCRs) in antigen recognition and immune response, this study investigated the association between KD and viral infection through comparative analysis of TCR repertoires. Methods: TCR repertoires from KD patients, healthy children, and individuals with viral infections were comparatively analyzed. TCR diversity and V(D)J usage were assessed using Shannon’s entropy, the Mann–Whitney U test, and Fisher’s exact test. Positional motif enrichment analysis within CDR3 regions was performed based on paratope hotspot classification. Results: Relatively reduced TCR clonal abundance and diversity were observed in KD patients compared to healthy controls. While substantial overlap in VJ gene segment usage was detected between KD and cytomegalovirus (CMV) infection, limited overlap in clonal TCRαβ chains was found between KD and viral infection groups. A predominant TCR combination, TRAV14DV4-J13-TRBV20-1-J2-5, enriched with characteristic amino acid motifs (EET, YNE, LAG, GQG, and AYE), was frequently identified in KD. Conclusions: These observations suggest potential differences in TCR repertoire features between KD patients and both healthy and virus-infected groups. However, the relationship between KD pathogenesis and the viruses examined requires further investigation with larger cohorts.

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Cite This Study

Geng et al. (2026) studied this question.

synapsesocial.com/papers/69a91e4cd6127c7a504c217fhttps://doi.org/10.3390/biomedicines14030574
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