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Identification of a shared antigen linking CD4(+) T and B cell pathology in Sjögren's disease.
PubMed
Authors: Takeshita M, Inamo J, Wakui S, Nagashima R, Nishino T, Tsunoda K, Usuda S, Inokuchi H, Ishigaki K, Sasaki T, Kagoya Y, Suzuki K, Kaneko Y
Year
2026
Paper ID
68603
Status
Peer-reviewed
Abstract Read
~2 min
Abstract Words
172
Citations
N/A
Abstract
Sjögren's disease (SjD) is an autoimmune disorder characterized by lymphocytic infiltration of exocrine glands. Although B cells producing anti-Ro60 autoantibodies are frequently found in salivary gland lesions, the antigen specificity of CD4 T cells has remained unclear. Given accumulating evidence for T cell involvement in local autoantibody production, we comprehensively investigated Ro60 reactivity among lesion-infiltrating CD4 T cells. Over 200 T cell receptors (TCRs) enriched in salivary glands from Japanese and Caucasian patients with SjD were screened using a TCR reporter system, identifying 13 Ro60-reactive TCRs predominantly expressed in T peripheral helper/T follicular helper subset, along with human leukocyte antigen alleles linked to SjD susceptibility. Ro60 was efficiently phagocytosed by antigen-presenting cells in the presence of autoantibodies and presented to Ro60-specific T cells, triggering their activation. This suggests that Ro60-specific B and CD4 T cells orchestrate a pathological loop in salivary glands. Our study provides the first molecular identification of a major CD4 T cell antigen in systemic autoimmunity and highlights coordinated T-B cell responses against a shared autoantigen.
Why This Paper Matters
- This paper contributes to the Quantum Chemistry research area in the Quantum Articles archive.
- It adds a 2026 reference point for readers tracking recent quantum research.
- Sjögren's disease (SjD) is an autoimmune disorder characterized by lymphocytic infiltration of exocrine glands.
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