Regulatory T cells are expanded in blood and disease sites in patients with tuberculosis

V Guyot-Revol, JA Innes, S Hackforth… - American journal of …, 2006 - atsjournals.org
Rationale: T-cell responses during tuberculosis (TB) help contain Mycobacterium tuberculosis
in vivo but also cause collateral damage to host tissues. Immune regulatory mechanisms …

[HTML][HTML] Repeated nebulisation of non-viral CFTR gene therapy in patients with cystic fibrosis: a randomised, double-blind, placebo-controlled, phase 2b trial

…, SC Hyde, L Hyndman, JA Innes… - The Lancet …, 2015 - thelancet.com
Background Lung delivery of plasmid DNA encoding the CFTR gene complexed with a
cationic liposome is a potential treatment option for patients with cystic fibrosis. We aimed to …

Inappropriate inhaler use: assessment of use and patient preference of seven inhalation devices

J Lenney, JA Innes, GK Crompton - Respiratory medicine, 2000 - Elsevier
Inefficient inhaler technique is a common problem resulting in poor drug delivery, decreased
disease control and increased inhaler use. The aim of this study was to assess patients' use …

Evidence for reflex upper airway dilator muscle activation by sudden negative airway pressure in man.

RL Horner, JA Innes, K Murphy… - The Journal of …, 1991 - Wiley Online Library
1. To determine if negative upper airway pressure causes reflex pharyngeal dilator muscle
activation, we used intra‐oral bipolar surface electrodes to record genioglossus …

Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

…, LP Ho, JM Samways, M Imrie, AP Greening, JA Innes - Gene therapy, 1997 - nature.com
In cystic fibrosis (CF), mutation of the cystic fibrosis transmembrane conductance regulator (CFTR)
gene results in defective transepithelial ion transport, leading to life shortening …

Dynamic relationship between IFN-γ and IL-2 profile of Mycobacterium tuberculosis-specific T cells and antigen load

KA Millington, JA Innes, S Hackforth… - The Journal of …, 2007 - journals.aai.org
Distinct IFN-γ and IL-2 profiles of Ag-specific CD4+ T cells have recently been associated
with different clinical disease states and Ag loads in viral infections. We assessed the kinetics …

Airways in cystic fibrosis are acidified: detection by exhaled breath condensate

S Tate, G MacGregor, M Davis, JA Innes, AP Greening - Thorax, 2002 - thorax.bmj.com
Background: The loss of cystic fibrosis transmembrane conductance regulator (CFTR) mediated
chloride conductance does not fully explain the diverse pathologies evident in patients …

Lung clearance index is a sensitive, repeatable and practical measure of airways disease in adults with cystic fibrosis

…, JC Davies, S Cunningham, E Alton, JA Innes - Thorax, 2008 - thorax.bmj.com
Background: Lung clearance index (LCI) is a sensitive marker of early lung disease in children
but has not been assessed in adults. Measurement is hindered by the complexity of the …

Managing passengers with stable respiratory disease planning air travel: British Thoracic Society recommendations

…, AR Cummin, DP Gradwell, L Howard, JA Innes… - Thorax, 2011 - thorax.bmj.com
INTRODUCTION Need for new recommendations for managing passengers with respiratory
disease planning air travel Since the first British Thoracic Society (BTS) recommendations …

Cluster of human tuberculosis caused by Mycobacterium bovis: evidence for person-to-person transmission in the UK

…, EG Smith, A Banerjee, RMM Smith, J Dale, JA Innes… - The Lancet, 2007 - thelancet.com
Background Despite a recent resurgence in the incidence of bovine tuberculosis in UK cattle
herds, no associated rise in the number of cases in man has been noted. Disease due to …