CD4+LAG3+T cells are decreased in SSc-ILD and affect fibroblast mesenchymal transition by TGF-β3

Pulmonary fibrosis frequently occurs in rheumatic conditions, particularly systemic sclerosis-associated interstitial lung disease (SSc-ILD). The pathology involves cell transformation into interstitial structures and collagen accumulation. CD4+LAG3+T cells, known for immune inhibition, are relevant in autoimmunity. This study investigates CD4+LAG3+T cells in SSc-ILD. Clinical analysis revealed a correlation between CD4+LAG3+T cells and interleukin-6 (IL-6) and erythrocyte sedimentation rate (ESR). Using primary human lung fibroblasts (pHLFs) and murine bone marrow-derived macrophages (BMDMs), we showed that CD4+LAG3+T cells secreted TGF-β3 inhibits TGF-β1-induced mesenchymal transformation, modulates cellular function, and reduces collagen release. In mouse models, CD4+LAG3+T cells exhibited potential in alleviating bleomycin-induced pulmonary fibrosis. This study emphasizes CD4+LAG3+T cells’ therapeutic promise against fibrosis and proposes their role as biomarkers. [Display omitted] •Reduced CD4+LAG3+T cell in SSc-ILD correlate negatively with IL-6•CD4+LAG3+T cells block TGF-β1-induced mesenchymal transition in cells•CD4+LAG3+T cells hinder cell function and collagen secretion due to TGF-β1•CD4+LAG3+T cells ameliorate bleomycin-induced mouse pulmonary fibrosis Health sciences; Rheumatology; Fibrosis