Soluble interleukin-2 receptor in exhaled breath condensate in pulmonary sarcoidosis: a cross-sectional pilot study.


Journal

Journal of breath research
ISSN: 1752-7163
Titre abrégé: J Breath Res
Pays: England
ID NLM: 101463871

Informations de publication

Date de publication:
18 12 2020
Historique:
entrez: 18 12 2020
pubmed: 19 12 2020
medline: 22 6 2021
Statut: epublish

Résumé

Sarcoidosis is a chronic granulomatous disease of unknown aetiology with a variable clinical course and prognosis. There is an urgent need to identify new and novel biomarkers to help differentiate between clinical phenotypes and guide clinical decisions with respect to commencing and monitoring treatment. Across the spectrum of respiratory disease there has been a growing interest in the role of breath-based biomarkers given their non-invasive nature and ability to repeat sampling with ease for serial monitoring. Soluble interleukin-2 receptor (sIL2R) in bronchoalveolar lavage and serum correlates with disease activity in sarcoidosis; however, no previous study has evaluated sIL2R in exhaled breath. The main aim of this cross-sectional case-controlled pilot study was to determine the concentration of sIL2R in exhaled breath condensate (EBC) from patients with recently diagnosed sarcoidosis compared to healthy volunteers and to establish, if present, if this correlated with markers of disease activity, pulmonary function tests and serological markers used in current clinical practice. Paired serum and EBC samples were collected from twelve treatment naïve patients with histologically proven sarcoidosis diagnosed during the previous six months and compared to twelve healthy volunteers matched for age and gender. Mean concentration of serum sIL2R was significantly elevated in participants with sarcoidosis compared to healthy controls (1584.3 ± 489.1 versus 874.2 ± 235.7 pg mL Soluble interleukin-2 receptor is detectable in EBC; however, the findings from our study do not support its role as a diagnostic marker in sarcoidosis. Further research is required to evaluate its prognostic utility.

Identifiants

pubmed: 33336649
doi: 10.1088/1752-7163/abb763
doi:

Substances chimiques

Biomarkers 0
Receptors, Interleukin-2 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

016016

Subventions

Organisme : Department of Health
Pays : United Kingdom

Auteurs

Dayle L Terrington (DL)

Norwich Medical School, The University of East Anglia, Norwich, United Kingdom.
Norfolk and Norwich University Hospital NHS Foundation Trust, Norwich, United Kingdom.

Jee Whang Kim (JW)

Norwich Medical School, The University of East Anglia, Norwich, United Kingdom.
Norfolk and Norwich University Hospital NHS Foundation Trust, Norwich, United Kingdom.

Garth Ravenhill (G)

Norfolk and Norwich University Hospital NHS Foundation Trust, Norwich, United Kingdom.

Jonathan Tang (J)

Norwich Medical School, The University of East Anglia, Norwich, United Kingdom.

Isabelle Piec (I)

Norwich Medical School, The University of East Anglia, Norwich, United Kingdom.

Stephen J Fowler (SJ)

Division of Infection, Immunity and Respiratory Medicine, School of Biological Sciences, The University of Manchester; Manchester Academic Health Science Centre and NIHR Manchester Biomedical Research Centre, Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom.

William Fraser (W)

Norwich Medical School, The University of East Anglia, Norwich, United Kingdom.
Norfolk and Norwich University Hospital NHS Foundation Trust, Norwich, United Kingdom.

Andrew M Wilson (AM)

Norwich Medical School, The University of East Anglia, Norwich, United Kingdom.
Norfolk and Norwich University Hospital NHS Foundation Trust, Norwich, United Kingdom.

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Classifications MeSH