BOS is associated with decreased HDAC2 from steroid resistant lymphocytes in the small airways. (29th October 2018)

• Record Type: Journal Article
• Authors: Hodge, G; Hodge, S; Yeo, A; Nguyen, P; Hopkins, E; Liu, H; Holmes-Liew, C L; Holmes, M
• Is Part Of: Clinical and experimental immunology. Volume 195:Number 2(2019)
• Page Start: 277
• Page End: 285
• Publication Date: 2018-10-29
• Subjects: bronchiolitis obliterans syndrome -- CD8+ T and NK T-like -- histone deacetylase 2 -- proinflammatory lymphocytes -- small airways; Immunopathology -- Periodicals; 616.079
• DOI: 10.1111/cei.13221
• Languages: English
• ISSNs: 0009-9104

Abstract

Summary: Immunosuppression therapies including corticosteroids fail to prevent bronchiolitis obliterans syndrome (BOS), primarily a disease of the small airways, following lung transplantation. We reported increases in steroid-resistant proinflammatory lymphocytes and their loss of histone deacetylase 2 (HDAC2), an important mediator of steroid action, in the blood of stable lung transplant recipients. We noted similar increases in the steroid-resistant lymphocytes in both the blood and small airways in BOS compared with the large airways. We hypothesized that these small airway cells would also exhibit a loss of HDAC2, and that these changes could be reversed by treatment with theophylline (HDAC2 activator). Blood, bronchoalveolar lavage and large and small airway brushings were collected from lung transplant patients with BOS ( n = 12) or stable lung function ( n = 18) and healthy aged-matched controls ( n = 13). Intracellular proinflammatory cytokines [interferon (IFN-γ) and tumour necrosis factor (TNF)-α and HDAC2 were measured in CD8 + T, natural killer (NK) T-like and NK cells from cultured small airway brushings ± 5 mg/l theophylline ± 1 µM prednisolone using flow cytometry. Increased small airway CD8 T, NK T-like and NK cells were identified in BOS versus stable transplant and controls. In BOS, these cells exhibited increased IFN-γ/TNF-α and a loss of HDAC2. HDAC2 expression by small airway CD8 + T cells correlated with forced expiratory volume in 1 s (FEV1 ) ( R = 0·880, P = 0·031). Theophylline and prednisolone synergistically up-regulated HDAC2 in CD8 + T cells. BOS is associated with loss of HDAC2 from steroid-resistant proinflammatory CD8 + T, NK T-like and NK cells in the small airways. Therapeutically increasing HDAC2 in these lymphocytes may reduce steroid resistance and improve graft survival. Graphical Abstract: