Masaru Takeshita, Jun Inamo, 和久井世紀, Ryosuke Nagashima, Takahiro Nishino, Kazuyuki Tsunoda, Satoshi Usuda, Hajime Inokuchi, Kazuyoshi Ishigaki, Takashi Sasaki, Yuki Kagoya, Katsuya Suzuki, Yuko Kaneko
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.