Journal Article

Anti-CXCL4 Antibody Reactivity Is Present in Systemic Sclerosis (SSc) and Correlates with the SSc Type I Interferon Signature

Mennella, Anna, Palazzo, Raffaella, Boirivant, Monica, Riccieri, Valeria, Chizzolini, Carlo, Stefanantoni, Katia, Pica, Roberta, Frasca, Loredana, Pietraforte, Immacolata, Butera, Alessia, Lande, Roberto, Conrad, Curdin, Iannace, Nicoletta

2020

Overview

Systemic sclerosis (SSc) is characterized by skin/internal organ fibrosis, vasculopathy and autoimmunity. Chemokine (C-X-C motif) ligand 4 (CXCL4) is an SSc biomarker, predicting unfavorable prognosis and lung fibrosis. CXCL4 binds DNA/RNA and favors interferon (IFN)-α production by plasmacytoid dendritic cells (pDCs), contributing to the type I IFN (IFN-I) signature in SSc patients. However, whether CXCL4 is an autoantigen in SSc is unknown. Here, we show that at least half of SSc patients show consistent antibody reactivity to CXCL4. T-cell proliferation to CXCL4, tested in a limited number of patients, correlates with anti-CXCL4 antibody reactivity. Antibodies to CXCL4 mostly correlate with circulating IFN-α levels and are significantly higher in patients with lung fibrosis in two independent SSc cohorts. Antibodies to CXCL4 implement the CXCL4–DNA complex’s effect on IFN-α production by pDCs; CXCL4–DNA/RNA complexes stimulate purified human B-cells to become antibody-secreting plasma cells in vitro. These data indicate that CXCL4 is indeed an autoantigen in SSc and suggest that CXCL4, and CXCL4-specific autoantibodies, can fuel a harmful loop: CXCL4–DNA/RNA complexes induce IFN-α in pDCs and direct B-cell stimulation, including the secretion of anti-CXCL4 antibodies. Anti-CXCL4 antibodies may further increase pDC stimulation and IFN-α release in vivo, creating a vicious cycle which sustains the SSc IFN-I signature and general inflammation.

• Publisher: MDPI AG,MDPI
• Subject: Adaptive Immunity / Adult / Aged / Antibodies / Antibody Specificity / Autoantibodies - blood / Autoantigens - immunology / B-Lymphocytes - immunology / Biomarkers - blood / Case-Control Studies / Cell Proliferation / Colitis, Ulcerative - immunology / Dendritic Cells - immunology / Deoxyribonucleic acid / Disease / DNA / DNA - immunology / Female / Healthy Volunteers / Humans / Immunity, Innate / Immunologic Memory / In Vitro Techniques / Interferon / Interferon Type I - blood / Interferon-alpha - blood / Male / Middle Aged / Pathogenesis / Plasma / Platelet Factor 4 - immunology / Scleroderma / Scleroderma, Systemic - immunology / T-Lymphocytes - immunology