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Serial characterisation of monocyte and neutrophil function after lung resection
  1. Richard O Jones1,2,
  2. Mairi Brittan1,
  3. Niall H Anderson3,
  4. Andrew Conway Morris1,4,
  5. John T Murchison5,
  6. William S Walker2 and
  7. A John Simpson1,6
  1. 1The University of Edinburgh/Medical Research Council Centre for Inflammation Research, The Queen's Medical Research Institute, Edinburgh, UK
  2. 2Department of Thoracic Surgery, The Royal Infirmary of Edinburgh, Edinburgh, UK
  3. 3Centre for Population Health Sciences, The University of Edinburgh, Medical School, Edinburgh, UK
  4. 4Department of Anaesthesia, University of Cambridge, Cambridge Biomedical Campus, Hills Road, Cambridge, UK
  5. 5Department of Radiology, The Royal Infirmary of Edinburgh, Edinburgh, UK
  6. 6Institute of Cellular Medicine, Medical School, Newcastle University, Newcastle upon Tyne, UK
  1. Correspondence to Professor A John Simpson; j.simpson{at}ncl.ac.uk

Abstract

Objectives The primary aim of this prospective study was to perform a comprehensive serial characterisation of monocyte and neutrophil function, circulating monocyte subsets, and bronchoalveolar lavage (BAL) fluid after lung resection. A secondary aim was to perform a pilot, hypothesis-generating evaluation of whether innate immune parameters were associated with postoperative pneumonia.

Methods Forty patients undergoing lung resection were studied in detail. Blood monocytes and neutrophils were isolated preoperatively and at 6, 24 and 48 h postoperatively. BAL was performed preoperatively and immediately postoperatively. Monocyte subsets, monocyte responsiveness to lipopolysaccharide (LPS) and neutrophil phagocytic capacity were quantified at all time points. Differential cell count, protein and cytokine concentrations were measured in BAL. Pneumonia evaluation at 72 h was assessed using predefined criteria.

Results After surgery, circulating subsets of classical and intermediate monocytes increased significantly. LPS-induced release of proinflammatory cytokines from monocytes increased significantly and by 48 h a more proinflammatory profile was found. Neutrophil phagocytosis demonstrated a small but significant fall. Factors associated with postoperative pneumonia were: increased release of specific proinflammatory and anti-inflammatory cytokines from monocytes; preoperative neutrophilia; and preoperative BAL cell count.

Conclusions We conclude that postoperative lung inflammation is associated with specific changes in the cellular innate immune response, a better understanding of which may improve patient selection and prediction of complications in the future.

  • Innate Immunity
  • Thoracic Surgery

This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/

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