Pulmonary monocyte kinetics in healthy volunteers and subjects with inflammatory arthritis

Monocytes are central to innate and adaptive immunity, regulating tissue homeostasis and inflammation. However, data on their steady-state biodistribution in healthy humans are limited. We developed a non-invasive method to track radiolabelled autologous monocytes. Monocytes showed distinct intravascular transit kinetics vs neutrophils, with 45 min recovery of 47% for neutrophils vs 7% for monocytes (p=0.008), indicating predominant distribution in marginated pools. In patients with psoriatic and rheumatoid arthritis but no documented lung disease, we observed preferential early retention of monocytes in the lungs (transit half-life 25.2 min vs 14.2 min; p=0.008) compared with healthy volunteers, with reduced intravascular recovery in patients with rheumatoid arthritis (4.3% vs 12%; p=0.0043). These findings provide the first direct evidence of human monocyte pulmonary transit kinetics, systemic biodistribution and fate in health and inflammatory disease, advancing understanding of in vivo monocyte biology.

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Publication Details

Journal
Thorax
Published
2026-06-29
DOI
https://doi.org/10.1136/thorax-2025-224226
Primary Topic
Immune cells in cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

Pulmonary monocyte kinetics in healthy volunteers and subjects with inflammatory arthritis

Rebecca C. Furze, Nicholas Shenker, Charlotte Summers, Flavia Sunzini et al.
Thorax
Immune cells in cancer
article

Pulmonary monocyte kinetics in healthy volunteers and subjects with inflammatory arthritis

Rebecca C. Furze, Nicholas Shenker, Charlotte Summers, Flavia Sunzini, Huw D. Lewis, Joseph Hutton, Neda Farahi, Edwin R. Chilvers, Daniel Gillett, Alex Tate, Richard Hohne, Jonathan Cavanagh, Anthony YKC Ng
article en

Abstract

Monocytes are central to innate and adaptive immunity, regulating tissue homeostasis and inflammation. However, data on their steady-state biodistribution in healthy humans are limited. We developed a non-invasive method to track radiolabelled autologous monocytes. Monocytes showed distinct intravascular transit kinetics vs neutrophils, with 45 min recovery of 47% for neutrophils vs 7% for monocytes (p=0.008), indicating predominant distribution in marginated pools. In patients with psoriatic and rheumatoid arthritis but no documented lung disease, we observed preferential early retention of monocytes in the lungs (transit half-life 25.2 min vs 14.2 min; p=0.008) compared with healthy volunteers, with reduced intravascular recovery in patients with rheumatoid arthritis (4.3% vs 12%; p=0.0043). These findings provide the first direct evidence of human monocyte pulmonary transit kinetics, systemic biodistribution and fate in health and inflammatory disease, advancing understanding of in vivo monocyte biology.

Thorax
GlaxoSmithKline (United Kingdom) (GB), University of Cambridge (GB), Cambridge University Hospitals NHS Foundation Trust (GB), Cambridge University Health Partners (GB), Imperial College London (GB), University of Glasgow (GB)
GlaxoSmithKline, Wellcome Trust, UK Research and Innovation, National Institute for Health and Care Research, Evelyn Trust, Medical Research Council, NIHR Cambridge Biomedical Research Centre
Good health and well-being
Openalex Percentile: Top 11%
Immune cells in cancer
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