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TIM-3-driven macrophage polarisation is associated to recalcitrant chronic rhinosinusitis with nasal polyps
Objective:
This study evaluated the expression of TIM-3 and its influence on macrophage polarisation in recalcitrant chronic rhinosinusitis with nasal polyps (CRSwNP).
Methods:
We detected TIM-3 expression in serum and tissue samples of healthy controls (HC), primary CRSwNP, and patients with recurrent CRSwNP. Macrophage markers were detected among three groups, and their correlations with TIM-3 levels were examined. Macrophages from circulating blood were collected and used to examine the impact of TIM-3 on polarisation in vitro.
Results:
TIM-3 levels were enhanced in the CRSwNP group compared to the HC group. Tissue immunofluorescence revealed elevated TIM-3 expression in patients with CRSwNP, and patients with multiple recurrences exhibited higher TIM-3 levels compared to their first recurrence and baseline levels. Tissue CD163 and CD206 levels were higher in recurrent CRSwNP in comparison with primary cases and HCs, and had a positive correlation with TIM-3 levels. TIM-3 overexpression promoted M2 polarisation and enhanced TGF-β1 and IL-10 secretion.
Conclusions:
TIM-3 expression was enhanced in patients with CRSwNP, especially in those undergoing revision surgeries. TIM-3 may be a novel biomarker for recalcitrant CRSwNP. TIM-3-driven M2 polarisation might be involved in the mechanisms of recurrent CRSwNP.
Insights
T-cell immunoglobulin and mucin-domain containing-3 (TIM-3) expression is elevated in chronic rhinosinusitis with nasal polyps (CRSwNP), particularly in recurrent cases. TIM-3 promotes M2 macrophage polarization, suggesting its role in recalcitrant CRSwNP.
Area of Science:
- Immunology
- Otolaryngology
- Pathophysiology
Background:
- Chronic rhinosinusitis with nasal polyps (CRSwNP) is a complex inflammatory condition.
- Recalcitrant CRSwNP, especially following revision surgery, presents significant clinical challenges.
- The role of specific immune markers like TIM-3 in CRSwNP pathogenesis remains incompletely understood.
Purpose of the Study:
- To evaluate the expression of T-cell immunoglobulin and mucin-domain containing-3 (TIM-3) in patients with CRSwNP.
- To investigate the influence of TIM-3 on macrophage polarization in CRSwNP.
- To explore TIM-3 as a potential biomarker for recalcitrant CRSwNP.
Main Methods:
- TIM-3 expression was quantified in serum and tissue samples from healthy controls (HC), primary CRSwNP, and recurrent CRSwNP patients.
- Macrophage polarization markers (CD163, CD206) were assessed and correlated with TIM-3 levels.
- In vitro experiments examined the effect of TIM-3 overexpression on macrophage polarization and cytokine secretion (TGF-β1, IL-10).
Main Results:
- TIM-3 levels were significantly higher in CRSwNP patients compared to HCs, with elevated expression in recurrent cases.
- Tissue immunofluorescence confirmed increased TIM-3 expression in CRSwNP, correlating positively with CD163 and CD206.
- TIM-3 overexpression induced M2 macrophage polarization and increased secretion of TGF-β1 and IL-10.
Conclusions:
- Elevated TIM-3 expression is associated with CRSwNP, particularly in patients requiring revision surgery.
- TIM-3 may serve as a novel biomarker for identifying and managing recalcitrant CRSwNP.
- TIM-3-mediated M2 macrophage polarization is implicated in the pathophysiology of recurrent CRSwNP.
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