Association of Th2-like inflammation with a Tfh/Tph–germinal center immune programs in submandibular gland lesions of IgG4-related disease

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ID: 323206
2026
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Abstract
OBJECTIVES: IgG4-related disease (IgG4-RD) has long been associated with Th2-predominant immune responses and allergic features. However, the immunological context underlying lesional Th2-like inflammation remains incompletely understood. METHODS: Bulk RNA-seq data from 49 submandibular gland lesions of IgG4-RD were analyzed. Module scores representing Th2, Tfh/Tph, B cell, germinal center B cell (GC_B), plasma cell, macrophage, and stromal/fibrotic programs were calculated. Correlations between Th2 module scores and other immune/stromal modules were assessed using Spearman correlation analysis. Differentially expressed genes between Th2-high and Th2-low lesions were also evaluated. RESULTS: Th2 module scores were strongly associated with Tfh, Tfh/Tph, and Tph helper T cell programs, as well as with B cell, GC_B, and plasma cell signatures. In addition, Th2 module scores positively correlated with M2 macrophage and fibrosis-associated macrophage (FAM) programs. Differential expression analysis demonstrated increased expression of chronic helper T cell-related genes, including PDCD1, TOX, and MAF, together with plasmablast-associated genes such as JCHAIN, MZB1, and PRDM1 in Th2-high lesions. In contrast, serum IgG4 and IgE levels did not significantly differ between Th2-high and Th2-low groups. CONCLUSIONS: Lesional Th2-like inflammation in IgG4-RD was closely associated with chronic Tfh/Tph-germinal center immune programs linked to plasmablast and M2/FAM macrophage responses. No clear association with available systemic allergy-related parameters was observed in this cohort.
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openalex_W7172122329 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Motohisa Yamamoto, Ryuta Kamekura, Masaaki Uehara, Yuta Ichii, Kenichi Takano
Journal Lara D. Veeken
Year 2026
DOI
10.1093/rheumatology/keag394
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Keywords Keywords not found

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