Examines monocyte transit in healthy volunteers and arthritis patients, indicating key differences in retention.
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 radiolabeled autologous monocytes. Monocytes showed distinct intravascular transit kinetics versus neutrophils, with 45 min recovery of 47% for neutrophils versus 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 to 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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Farahi et al. (2026) studied this question.
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