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Updated: Dec 24, 2025

Characterization of Human Monocyte Subsets by Whole Blood Flow Cytometry Analysis
Published on: October 17, 2018
Clinical features and monocyte/macrophage subsets characterization in granulomatous vs non-granulomatous Crohn's
1Department of Gastroenterology, West China Hospital, Sichuan University, Chengdu, China.
Insights
Granuloma presence in Crohn's disease (CD) indicates distinct clinical features and altered monocyte/macrophage profiles. Granulomatous CD patients may require more aggressive treatment due to these differences.
Area of Science:
- Gastroenterology
- Immunology
- Histopathology
Background:
- Granulomas, macrophage aggregates, are a hallmark of Crohn's disease (CD).
- The clinical significance and underlying immunological differences of granulomatous CD remain under-investigated.
Purpose of the Study:
- To compare clinical, endoscopic, and histopathological features between granulomatous and non-granulomatous CD.
- To investigate differences in monocyte/macrophage subsets, phagocytic capacity, and plasma cytokine profiles.
Main Methods:
- Comparative analysis of 222 CD patients (90 with granulomas) using clinical data, Montreal classification, and histopathology.
- Flow cytometry for monocyte subset analysis and phagocytosis assessment.
- ELISA and immunohistochemistry for plasma cytokine levels and macrophage marker expression (CD68, CD163, iNOS).
Main Results:
- Granulomatous CD patients presented with younger age, more diarrhea, perianal disease, higher endoscopic scores, intestinal stenosis, and crypt abscesses.
- Defective monocyte phagocytosis, altered monocyte subsets (increased intermediate/non-classic, decreased classic), and elevated TGF-β1/IL-10 with reduced TNF-α were observed.
- Increased CD163+/CD68+ and decreased iNOS+/CD68+ ratios indicated a shift towards an anti-inflammatory macrophage phenotype.
Conclusions:
- Granulomatous CD is clinically distinct from non-granulomatous CD, suggesting a more aggressive disease course.
- Heterogeneity in monocyte/macrophage subsets and altered cytokine profiles contribute to the distinct phenotypes.
- Granulomatous CD may necessitate tailored, more aggressive therapeutic strategies.
Abstract:
Aims: Granuloma, mainly composed of macrophages, is a histological feature of Crohn's disease (CD). However, its significance in CD has not been investigated adequately. Our study aims to address this issue by comparing the clinical manifestations and monocyte/macrophage subtypes between granulomatous and non-granulomatous CD.Materials and methods: Demographics, symptoms, endoscopic manifestations, histopathological features, and Montreal classification of patients with and without granulomas were compared. Flow cytometry was used to determine the phagocytosis and subsets of monocytes. ELISA was used to measure the plasma levels of TNF-α, IL-6, IL-1β, IL-10, CCL22, and TGF-β1. Immunohistochemistry was performed to quantify the expression of CD68, CD163 and iNOS.Results: Of the222 CD patients enrolled, granulomas were detected in 90. Compared with non-granulomatous CD patients, those with granulomas had younger age, increased rates of diarrhea and perianal complications, along with higher endoscopic score. Intestinal stenosis and crypt abscess were more frequently observed in granulomatous CD patients. A defective phagocytosis of monocytes was observed in granulomatous CD patients. Meanwhile, higher percentages of intermediate and non-classic monocytes, with a lower percentage of classic monocyte were found in them. Besides, they had higher levels of TGF-β1 and IL-10, a lower level of TNF-α, an increased ratio of CD163+/CD68+cells, and a decreased ratio of iNOS+/CD68+ cells.Conclusions: Granulomatous CD patients exhibited different manifestations compared with their non-granulomatous counterparts. More aggressive therapy may be needed in granulomatous CD patients. Furthermore, the heterogeneity of monocyte/macrophage subsets and altered plasma cytokine may underlie the difference between those two groups.
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