Journal article
PD-1 up-regulation on CD4 + T cells promotes pulmonary fibrosis through STAT3-mediated IL-17A and TGF-β1 production
Science Translational Medicine, Vol.10(460)
2018
Abstract
Pulmonary fibrosis is a progressive inflammatory disease with high mortality and limited therapeutic options. Previous genetic and immunologic investigations suggest common intersections between idiopathic pulmonary fibrosis (IPF), sarcoidosis, and murine models of pulmonary fibrosis. To identify immune responses that precede collagen deposition, we conducted molecular, immunohistochemical, and flow cytometric analysis of human and murine specimens. Immunohistochemistry revealed programmed cell death-1 (PD-1) up-regulation on IPF lymphocytes. PD-1+CD4+ T cells with reduced proliferative capacity and increased transforming growth factor–β (TGF-β)/interleukin-17A (IL-17A) expression were detected in IPF, sarcoidosis, and bleomycin CD4+ T cells. PD-1+ T helper 17 cells are the predominant CD4+ T cell subset expressing TGF-β. Coculture of PD-1+CD4+ T cells with human lung fibroblasts induced collagen-1 production. Strikingly, ex vivo PD-1 pathway blockade resulted in reductions in TGF-β and IL-17A expression from CD4+ T cells, with concomitant declines in collagen-1 production from fibroblasts. Molecular analysis demonstrated PD-1 regulation of the transcription factor STAT3 (signal transducer and activator of transcription 3). Chemical blockade of STAT3, using the inhibitor STATTIC, inhibited collagen-1 production. Both bleomycin administration to PD-1 null mice or use of antibody against programmed cell death ligand 1 (PD-L1) demonstrated significantly reduced fibrosis compared to controls. This work identifies a critical, previously unrecognized role for PD-1+CD4+ T cells in pulmonary fibrosis, supporting the use of readily available therapeutics that directly address interstitial lung disease pathophysiology.
Details
- Title
- PD-1 up-regulation on CD4 + T cells promotes pulmonary fibrosis through STAT3-mediated IL-17A and TGF-β1 production
- Authors/Creators
- L.J. Celada (Author/Creator) - Vanderbilt UniversityJ.A. Kropski (Author/Creator) - Vanderbilt UniversityJ.D. Herazo-Maya (Author/Creator) - Yale UniversityW. Luo (Author/Creator) - Vanderbilt UniversityA. Creecy (Author/Creator) - Oklahoma Medical Research FoundationA.T. Abad (Author/Creator) - Vanderbilt UniversityO.S. Chioma (Author/Creator) - Vanderbilt UniversityG. Lee (Author/Creator) - Vanderbilt UniversityN.E. Hassell (Author/Creator) - Vanderbilt UniversityG.I. Shaginurova (Author/Creator) - Vanderbilt UniversityY. Wang (Author/Creator) - Vanderbilt UniversityJ.E. Johnson (Author/Creator) - Vanderbilt UniversityA. Kerrigan (Author/Creator) - Vanderbilt UniversityW.R. Mason (Author/Creator) - Vanderbilt UniversityR.P. Baughman (Author/Creator) - University of CincinnatiG.D. Ayers (Author/Creator) - Vanderbilt UniversityG.R. Bernard (Author/Creator) - Vanderbilt UniversityD.A. Culver (Author/Creator) - Cleveland ClinicC.G. Montgomery (Author/Creator) - Oklahoma Medical Research FoundationT.M. Maher (Author/Creator) - National Institute for Health ResearchP.L. Molyneaux (Author/Creator) - National Institute for Health ResearchI. Noth (Author/Creator) - University of ChicagoS.E. Mutsaers (Author/Creator) - The University of Western AustraliaC.M. Prêle (Author/Creator) - The University of Western AustraliaR. Stokes Peebles (Author/Creator)D.C. Newcomb (Author/Creator) - Vanderbilt UniversityN. Kaminski (Author/Creator) - Yale UniversityT.S. Blackwell (Author/Creator) - Vanderbilt UniversityL. Van Kaer (Author/Creator) - Vanderbilt UniversityW.P. Drake (Author/Creator) - Vanderbilt University
- Publication Details
- Science Translational Medicine, Vol.10(460)
- Publisher
- AAAS
- Identifiers
- 991005540763307891
- Copyright
- © 2018 American Association for the Advancement of Science
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
UN Sustainable Development Goals (SDGs)
This output has contributed to the advancement of the following goals:
Source: InCites
Metrics
79 Record Views
InCites Highlights
These are selected metrics from InCites Benchmarking & Analytics tool, related to this output
Highly Cited Paper
- Collaboration types
- Domestic collaboration
- International collaboration
- Citation topics
- 1 Clinical & Life Sciences
- 1.208 Vasculitis & Autoimmune Disorders
- 1.208.1262 Idiopathic Pulmonary Fibrosis
- Web Of Science research areas
- Cell Biology
- Medicine, Research & Experimental
- ESI research areas
- Biology & Biochemistry