S65 Quantification of 'whole lung' pulmonary eosinophilic inflammation using radiolabelled autologous human eosinophils. (15th November 2017)
- Record Type:
- Journal Article
- Title:
- S65 Quantification of 'whole lung' pulmonary eosinophilic inflammation using radiolabelled autologous human eosinophils. (15th November 2017)
- Main Title:
- S65 Quantification of 'whole lung' pulmonary eosinophilic inflammation using radiolabelled autologous human eosinophils
- Authors:
- Farahi, N
Loutsios, S
Tregay, N
Wright, AKA
Lok, LSC
Gillett, D
Cullum, I
Simmonds, RP
Summers, C
Wong, A
Solanki, CK
Buscombe, J
Pang, PH
Thavakumar, A
Peters, AM
Brightling, CE
Condliffe, AM
Chilvers, ER - Abstract:
- Abstract : Background: Eosinophils are key mediators of allergic inflammation. The ability to localise and quantify eosinophilic inflammation in vivo would facilitate patient endotyping and evaluation of eosinophil-targeted therapeutics. We aimed to quantify eosinophil distribution and organ-specific uptake in healthy subjects, asthmatics, and patients with focal pulmonary eosinophilic inflammation. Methods: We injected autologous radiolabelled eosinophils into 8 healthy volunteers, 15 asthmatics (7 obese and 7 non-obese), and 3 patients with focal eosinophilic inflammation and monitored eosinophil distribution (planar imaging, single photon emission computed tomography – SPECT)/CT). Lung accumulation of technetium-99 m-labelled eosinophils was quantified (Patlak-Rutland analysis). Whole body indium-111-labelled eosinophil distribution and loss were further assessed in 5 healthy volunteers and 7 asthmatics using a whole body counter. Findings: Pulmonary eosinophil clearance was increased in patients with focal eosinophilia (0·0033 ml/min/ml; 95% CI −0·005–0·011; p=0.02) compared to asthmatics (0·0007 ml/min/ml; 95% CI 0·0003–0·0010; p=0.14) and controls (0·0003 ml/min/ml; 95% CI −7·5 × 10 –5 –0·0008). Absolute lung eosinophil migration was elevated in patients with focal inflammation (5932 eosinophils/min/ml; 95% CI −14351–26215, p=0.01) and asthma (364 eosinophils/min/ml; 95% CI 38–689; p=0.03) versus healthy volunteers (38 eosinophils/min/ml; 95% CI −11–87). StratificationAbstract : Background: Eosinophils are key mediators of allergic inflammation. The ability to localise and quantify eosinophilic inflammation in vivo would facilitate patient endotyping and evaluation of eosinophil-targeted therapeutics. We aimed to quantify eosinophil distribution and organ-specific uptake in healthy subjects, asthmatics, and patients with focal pulmonary eosinophilic inflammation. Methods: We injected autologous radiolabelled eosinophils into 8 healthy volunteers, 15 asthmatics (7 obese and 7 non-obese), and 3 patients with focal eosinophilic inflammation and monitored eosinophil distribution (planar imaging, single photon emission computed tomography – SPECT)/CT). Lung accumulation of technetium-99 m-labelled eosinophils was quantified (Patlak-Rutland analysis). Whole body indium-111-labelled eosinophil distribution and loss were further assessed in 5 healthy volunteers and 7 asthmatics using a whole body counter. Findings: Pulmonary eosinophil clearance was increased in patients with focal eosinophilia (0·0033 ml/min/ml; 95% CI −0·005–0·011; p=0.02) compared to asthmatics (0·0007 ml/min/ml; 95% CI 0·0003–0·0010; p=0.14) and controls (0·0003 ml/min/ml; 95% CI −7·5 × 10 –5 –0·0008). Absolute lung eosinophil migration was elevated in patients with focal inflammation (5932 eosinophils/min/ml; 95% CI −14351–26215, p=0.01) and asthma (364 eosinophils/min/ml; 95% CI 38–689; p=0.03) versus healthy volunteers (38 eosinophils/min/ml; 95% CI −11–87). Stratification of asthmatics based on BMI revealed increased pulmonary eosinophil clearance in obese (0·001 ml/min/ml; 95% CI 0·0007–0·001; p=0.02) versus non-obese asthmatics (0·0003 ml/min/ml; 95% CI −0·0002–0·0009). Interpretation: Eosinophil radiolabelling can quantify pulmonary eosinophilic inflammation, with the potential for patient endotyping and testing eosinophil-targeted treatments. Funding: Medical Research Council, Wellcome Trust, Asthma UK, Cambridge NIHR Biomedical Research Centre. … (more)
- Is Part Of:
- Thorax. Volume 72(2017)Supplement 3
- Journal:
- Thorax
- Issue:
- Volume 72(2017)Supplement 3
- Issue Display:
- Volume 72, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 72
- Issue:
- 3
- Issue Sort Value:
- 2017-0072-0003-0000
- Page Start:
- A41
- Page End:
- A41
- Publication Date:
- 2017-11-15
- Subjects:
- Chest -- Diseases -- Periodicals
Thorax
Chest -- Diseases
Periodicals
Periodicals
617.54 - Journal URLs:
- http://thorax.bmjjournals.com/contents-by-date.0.shtml ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/thoraxjnl-2017-210983.71 ↗
- Languages:
- English
- ISSNs:
- 0040-6376
- Deposit Type:
- Legaldeposit
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