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Single-cell analysis: a novel approach to tumour necrosis factor- synthesis and secretion in sarcoidosis

Interstitial Lung Disease Unit, Dept of Occupational and Environmental Medicine, Royal Brompton Hospital and National Heart and Lung Institute, London, UK

CORRESPONDENCE: R.M. du Bois, Interstitial Lung Disease Unit, Dept of Occupational and Environmental Medicine, Royal Brompton Hospital, London, UK, SW3 6NP. Fax: 44 2073518336. E-mail: r.dubois@rbh.nthames.nhs.uk

Keywords: haemolytic plaquemacrophagesmonocytessarcoidosistumour necrosis factor

Received: January 25, 2002
Accepted May 12, 2002

This study was supported by the Sir Jules Thorn Trust.

Tumour necrosis factor (TNF)- is thought to be a key early cytokine in the pathogenesis of sarcoidosis, despite conflicting data. Largely the product of mononuclear phagocyte activation, it is unclear whether TNF- production at disease sites is a feature of all mononuclear phagocytes that accumulate there or whether it is secreted by a subset of these cells. Using the reverse haemolytic plaque assay, the aims of this study were to determine if the upregulation of TNF- could be confirmed and to investigate whether this was monocyte or macrophage specific. The reverse haemolytic plaque assay allows the measurement of cytokine production at a single cell level.

A greater number of alveolar macrophages produced TNF- compared to autologous monocytes in sarcoidosis but not in controls and, based on cell size, it was confirmed that this was the product of more mature macrophages and that the secretion of TNF- by monocytes and macrophages was heterogeneous: not all monocytes and macrophages secrete TNF-. No differences in the average levels of TNF- secretion by peripheral blood monocytes or alveolar macrophages were observed.

This study has demonstrated that a subset of mononuclear phagocytes, mature macrophages, are responsible for tumour necrosis factor secretion and this could have implications for targeted management in sarcoidosis in the future.

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