Use of autologous 99mTechnetium-labelled neutrophils to quantify lung neutrophil clearance in COPD. Issue 7 (23rd January 2019)

• Record Type: Journal Article
• Authors: Tregay, Nicola; Begg, Malcolm; Cahn, Anthony; Farahi, Neda; Povey, Kathryn; Madhavan, Sujith; Simmonds, Rosalind; Gillett, Daniel; Solanki, Chandra; Wong, Anna; Maison, Joanna; Lennon, Mark; Bradley, Glyn; Jarvis, Emily; de Groot, Marius; Wilson, Fred; Babar, Judith; Peters, A Michael; Hessel, Edith M; Chilvers, Edwin R
• Is Part Of: Thorax. Volume 74:Issue 7(2019)
• Page Start: 659
• Page End: 666
• Publication Date: 2019-01-23
• Subjects: imaging/ct mri etc -- innate immunity -- neutrophil biology -- copd pathology; Chest -- Diseases -- Periodicals; Thorax; Chest -- Diseases; Periodicals; Periodicals; 617.54
• DOI: 10.1136/thoraxjnl-2018-212509
• Languages: English
• ISSNs: 0040-6376

Abstract

Abstract : Rationale: There is a need to develop imaging protocols which assess neutrophilic inflammation in the lung. Aim: To quantify whole lung neutrophil accumulation in (1) healthy volunteers (HV) following inhaled lipopolysaccharide (LPS) or saline and (2) patients with COPD using radiolabelled autologous neutrophils and single-photon emission computed tomography/CT (SPECT/CT). Methods: 20 patients with COPD (Global initiative for chronic obstructive lung disease (GOLD) stages 2–3) and 18 HVs were studied. HVs received inhaled saline (n=6) or LPS (50 µg, n=12) prior to the injection of radiolabelled cells. Neutrophils were isolated using dextran sedimentation and Percoll plasma gradients and labelled with 99m Technetium (Tc)-hexamethylpropyleneamine oxime. SPECT was performed over the thorax/upper abdomen at 45 min, 2 hours, 4 hours and 6 hours. Circulating biomarkers were measured prechallenge and post challenge. Blood neutrophil clearance in the lung was determined using Patlak-Rutland graphical analysis. Results: There was increased accumulation of 99m Tc-neutrophils in the lungs of patients with COPD and LPS-challenged subjects compared with saline-challenged subjects (saline: 0.0006±0.0003 mL/min/mL lung blood distribution volume [mean ±1 SD]; COPD: 0.0022±0.0010 mL/min/mL [p<0.001]; LPS: 0.0025±0.0008 mL/min/mL [p<0.001]). The accumulation of labelled neutrophils in 10 patients with COPD who underwent repeat radiolabelling/imaging 7–10 days later was highly reproducible (0.0022±0.0010 mL/min/mL vs 0.0023±0.0009 mL/min/mL). Baseline interleukin (IL)-6 levels in patients with COPD were elevated compared with HVs (1.5±1.06 pg/mL [mean ±1 SD] vs 0.4±0.24 pg/mL). LPS challenge increased the circulating IL-6 levels (7.5±2.72 pg/mL) 9 hours post challenge. Conclusions: This study shows the ability to quantify 'whole lung' neutrophil accumulation in HVs following LPS inhalation and in subjects with COPD using autologous radiolabelled neutrophils and SPECT/CT imaging. Moreover, the reproducibility observed supports the feasibility of using this approach to determine the efficacy of therapeutic agents aimed at altering neutrophil migration to the lungs.