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Human Lung Conventional Dendritic Cells Orchestrate Lymphoid Neogenesis during Chronic Obstructive Pulmonary Disease.
Naessens, Thomas; Morias, Yannick; Hamrud, Eva; Gehrmann, Ulf; Budida, Ramachandramouli; Mattsson, Johan; Baker, Tina; Skogberg, Gabriel; Israelsson, Elisabeth; Thörn, Kristofer; Schuijs, Martijn J; Angermann, Bastian; Melville, Faye; Staples, Karl J; Cunoosamy, Danen M; Lambrecht, Bart N.
Afiliación
  • Naessens T; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Morias Y; Bioscience Cardiovascular, Research and Early Development, Cardiovascular, Renal and Metabolism (CVRM), and.
  • Hamrud E; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Gehrmann U; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Budida R; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Mattsson J; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Baker T; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity, BioPharmaceuticals R&D, AstraZeneca, Cambridge, United Kingdom.
  • Skogberg G; Bioscience COPD/IPF, Research and Early Development, Respiratory, Inflammation, Autoimmunity, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.
  • Israelsson E; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Thörn K; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Schuijs MJ; Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, United Kingdom.
  • Angermann B; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Melville F; Faculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom.
  • Staples KJ; Faculty of Medicine, Clinical and Experimental Sciences, University of Southampton, Southampton, United Kingdom.
  • Cunoosamy DM; Translational Science and Experimental Medicine, Research and Early Development, Respiratory, Inflammation, Autoimmunity.
  • Lambrecht BN; Laboratory of Immunoregulation, VIB-UGhent Center for Inflammation Research, Ghent, Belgium.
Am J Respir Crit Care Med ; 202(4): 535-548, 2020 08 15.
Article en En | MEDLINE | ID: mdl-32255375
ABSTRACT
Rationale Emerging evidence supports a crucial role for tertiary lymphoid organs (TLOs) in chronic obstructive pulmonary disease (COPD) progression. However, mechanisms of immune cell activation leading to TLOs in COPD remain to be defined.

Objectives:

To examine the role of lung dendritic cells (DCs) in T follicular helper (Tfh)-cell induction, a T-cell subset critically implicated in lymphoid organ formation, in COPD.

Methods:

Myeloid cell heterogeneity and phenotype were studied in an unbiased manner via single-cell RNA sequencing on HLA-DR+ cells sorted from human lungs. We measured the in vitro capability of control and COPD lung DC subsets, sorted using a fluorescence-activated cell sorter, to polarize IL-21+CXCL13+ (IL-21-positive and C-X-C chemokine ligand type 13-positive) Tfh-like cells. In situ imaging analysis was performed on Global Initiative for Chronic Obstructive Lung Disease stage IV COPD lungs with TLOs.Measurements and Main

Results:

Single-cell RNA-sequencing analysis revealed a high degree of heterogeneity among human lung myeloid cells. Among these, conventional dendritic type 2 cells (cDC2s) showed increased induction of IL-21+CXCL13+ Tfh-like cells. Importantly, the capacity to induce IL-21+ Tfh-like cells was higher in cDC2s from patients with COPD than in those from control patients. Increased Tfh-cell induction by COPD cDC2s correlated with increased presence of Tfh-like cells in COPD lungs as compared with those in control lungs, and cDC2s colocalized with Tfh-like cells in TLOs of COPD lungs. Mechanistically, cDC2s exhibited a unique migratory signature and (transcriptional) expression of several pathways and genes related to DC-induced Tfh-cell priming. Importantly, blocking the costimulatory OX40L (OX40 ligand)-OX40 axis reduced Tfh-cell induction by control lung cDC2s.

Conclusions:

In COPD lungs, we found lung EBI2+ (Epstein-Barr virus-induced gene 2-positive) OX-40L-expressing cDC2s that induced IL-21+ Tfh-like cells, suggesting an involvement of these cells in TLO formation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Dendríticas / Enfermedad Pulmonar Obstructiva Crónica / Estructuras Linfoides Terciarias / Pulmón Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Dendríticas / Enfermedad Pulmonar Obstructiva Crónica / Estructuras Linfoides Terciarias / Pulmón Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Respir Crit Care Med Asunto de la revista: TERAPIA INTENSIVA Año: 2020 Tipo del documento: Article
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