Related Experiment Video
Updated: Aug 17, 2026

An Immunohistopathologic Study to Profile the Folate Receptor Beta Macrophage and Vascular Immune Microenvironment in Giant Cell Arteritis
Published on: February 8, 2019
Macrophages overloaded with tissue debris in Wegener's granulomatosis
Z Mackiewicz1, A Rimkevicius, J Petersen
1Department of Pathology, Vilnius University Institute of Experimental and Clinical Medicine, Lithuania.
Objectives:
To analyse some scavenging related molecules in Wegener's granulomatosis (WG) macrophages.
Methods:
Immunohistochemical staining of lung, nasopharynx, and skin for macrophage markers related to scavenging (macrophage scavenger receptor MARCO, collagenase-1 and gelatinase-B), formation of multinuclear foreign body giant cells (ADAM 9/meltrin-gamma and ADAM 12/meltrin-alpha), and cell debris derived from neutrophils, endothelial cells and mast cells (specific granule protein 28 (SGP28), von Willebrand factor (vWF) and mast cell tryptase, respectively). TechMate staining robot and biotin-streptavidin protocol were used.
Results:
Some macrophages were activated and expressed collagenase-1 and gelatinase-B. Approximately 5% of macrophages expressed scavenger receptor, whereas 20-30% were meltrin positive. Interstitial and granuloma associated macrophages and giant cells contained partly undigested, immunoreactive SGP28-, vWF- and tryptase-positive cell rests and collagenous matrix. Lymphocytic follicles with germinal centres were found in the same areas.
Conclusion:
In WG tissue lesions macrophage and giant cells seem to be overwhelmed by the bulk to be scavenged. Despite cellular activation and continuing maturation to professional scavenger receptor (MARCO) and meltrin positive multinuclear giant cells combined with an organisation into granulomas, macrophages still contain partially undigested cell and tissue rests. This necrotic and damaged self may be the driving force for the formation of giant cell ("foreign body") granulomas. This, together with the local formation of secondary lymphatic follicles (with germinal centres), indicates active local antigen processing and presentation.
Insights
In Wegener's granulomatosis, macrophages and giant cells are overwhelmed by cellular debris, leading to granuloma formation. This suggests active antigen processing and presentation in affected tissues.
Area of Science:
- Immunology
- Pathology
Background:
- Wegener's granulomatosis (WG) is a complex inflammatory disease.
- Macrophages play a crucial role in immune responses and tissue repair.
Purpose of the Study:
- To investigate scavenging-related molecules and cellular debris within macrophages in WG lesions.
- To understand the role of macrophages and giant cells in WG pathogenesis.
Main Methods:
- Immunohistochemical staining of lung, nasopharynx, and skin tissues from WG patients.
- Analysis of macrophage markers (MARCO, collagenase-1, gelatinase-B), giant cell markers (ADAM 9, ADAM 12), and cell debris (SGP28, vWF, tryptase).
Main Results:
- Activated macrophages expressed collagenase-1 and gelatinase-B.
- Macrophages and giant cells contained undigested debris from neutrophils, endothelial cells, and mast cells.
- Lymphocytic follicles with germinal centers were observed in WG lesions.
Conclusions:
- Macrophages and giant cells in WG appear overwhelmed by the amount of cellular debris to be scavenged.
- Partially undigested necrotic self-material may drive foreign body giant cell granuloma formation.
- The presence of secondary lymphatic follicles indicates active local antigen processing and presentation in WG.
Related Concept Videos
Chronic Inflammation: Introduction
Acute Inflammation II: Cellular Phase

