Nuclear Medicine and Biology
Volume 35, Issue 8 , Pages 901-909, November 2008

PET scanning of macrophages in patients with scleroderma fibrosing alveolitis

  • Howard M. Branley

      Affiliations

    • Imperial College London, Hammersmith Campus, London, UK
    • Corresponding Author InformationCorresponding author. Department of Respiratory Medicine, The Whittington Hospital, Magdala Avenue, N19 5NF London, UK. Tel.: +44 20 7288 5272; fax: +44 20 7288 5060.
  • ,
  • Roland M. du Bois

      Affiliations

    • Royal Brompton Hospital, London, UK
  • ,
  • Athol U. Wells

      Affiliations

    • Royal Brompton Hospital, London, UK
  • ,
  • Hazel A. Jones

      Affiliations

    • Imperial College London, Hammersmith Campus, London, UK

Received 8 April 2008; received in revised form 11 August 2008; accepted 1 October 2008.

Abstract 

Rationale

Assessment of disease activity in fibrosing alveolitis due to systemic sclerosis (FASSc) is difficult without using invasive investigation. A repeatable noninvasive method of assessing disease at a cellular level such as with positron emission tomography (PET) could be of great value in evaluating high-resolution changes in the pathological process.

Objectives

To investigate whether the level of inflammatory cell traffic and lung density in FASSc, imaged in vivo by PET, is different to controls and whether they are associated with changes in pulmonary function indices.

Methods

We used PET to measure lung density and tissue uptake of 11C-[R]-PK11195, a ligand that binds to receptors found in abundance in macrophages. Fifteen patients with FASSc were compared to seven controls.

Results

A trend of reduced uptake of 11C-[R]-PK11195 was observed in FASSc patients (P=.09) and correlated inversely with lung density (r=−.62; P<.05), which was significantly elevated in FASSc [0.35±0.02 vs. 0.23±0.02 g/cc (mean±S.E.M.); P<.005].

Conclusion

These results demonstrate that inflammatory cell traffic and lung density can be imaged in vivo in FASSc using PET, and that this approach might be of potential value in understanding, in situ, components of pathogenesis that may have value for prognosis.

Keywords: PET scanning, Systemic sclerosis, Pulmonary fibrosis

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 This work was funded by the Raynaud's and Scleroderma Association of the United Kingdom.

PII: S0969-8051(08)00200-X

doi:10.1016/j.nucmedbio.2008.10.001

Nuclear Medicine and Biology
Volume 35, Issue 8 , Pages 901-909, November 2008