Autoantibodies are associated with disease progression in idiopathic pulmonary fibrosis

Several reports have highlighted a potential role of autoreactive B-cells and autoantibodies that correlates with increased disease severity in patients with idiopathic pulmonary fibrosis (IPF). Here we show that patients with IPF have an altered B-cell phenotype and that those subjects who have aut...

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Published inThe European respiratory journal Vol. 61; no. 5; p. 2102381
Main Authors Koether, Katerina, Besnard, Valérie, Sandig, Hilary, Carruthers, Alan, Miranda, Elena, Grootenboer-Mignot, Sabine, Taillé, Camille, Chevret, Sylvie, Valeyre, Dominique, Nunes, Hilario, Israel-Biet, Dominique, Lim, Wei Keat, Cottin, Vincent, Corkill, Dominic, Dobson, Claire, Groves, Maria, Ferraro, Franco, Guenzi, Edouard, Huang, Ling, Sulikowski, Michal, Mailleux, Arnaud, Murray, Lynne Anne, Mustelin, Thomas, Strickland, Ian, Sleeman, Matthew A., Crestani, Bruno
Format Journal Article
LanguageEnglish
Published England 01.05.2023
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ISSN0903-1936
1399-3003
1399-3003
DOI10.1183/13993003.02381-2021

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Summary:Several reports have highlighted a potential role of autoreactive B-cells and autoantibodies that correlates with increased disease severity in patients with idiopathic pulmonary fibrosis (IPF). Here we show that patients with IPF have an altered B-cell phenotype and that those subjects who have autoantibodies against the intermediate filament protein periplakin (PPL) have a significantly worse outcome in terms of progression-free survival. Using a mouse model of lung fibrosis, we demonstrate that introducing antibodies targeting the endogenous protein PPL (mimicking naturally occurring autoantibodies seen in patients) directly in the lung increases lung injury, inflammation, collagen and fibronectin expression through direct activation of follicular dendritic cells, which in turn activates and drives proliferation of fibroblasts. This fibrocyte population was also observed in fibrotic foci of patients with IPF and was increased in peripheral blood of IPF patients compared to aged-matched controls. This study reiterates the complex and heterogeneous nature of IPF, identifying new pathways that may prove suitable for therapeutic intervention.
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ISSN:0903-1936
1399-3003
1399-3003
DOI:10.1183/13993003.02381-2021