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Related Concept Videos

Complement System01:27

Complement System

The complement system is a group of approximately 20 plasma proteins that strengthen the body's defenses against infections through opsonization, inflammation, and cell lysis. Opsonization involves coating pathogens with complement proteins, making them more recognizable and facilitating phagocyte engulfment. Certain complement proteins induce inflammation that attracts immune cells to the site of infection. Cell lysis involves the destruction of pathogens through the formation of a membrane...
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Chronic bronchitis is a key phenotype of chronic obstructive pulmonary disease (COPD), characterized by airway-centered inflammation and mucus overproduction. It develops from long-term exposure to harmful particles or gases, most commonly cigarette smoke, which triggers a persistent inflammatory response.Cellular and Structural ChangesInflammation initially affects the large bronchi and later the smaller airways, with infiltration by immune cells, including neutrophils, macrophages, and...

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Updated: Jun 22, 2026

Immunofluorescent Labeling in Nasal Mucosa Tissue Sections of Allergic Rhinitis Rats via Multicolor Immunoassay
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Published on: September 22, 2023

Local complement activation in nasal polyposis.

Thibaut Van Zele1, Frauke Coppieters, Philippe Gevaert

  • 1Upper Airway Research Laboratory, Department of Otorhinolaryngology, Ghent University Hospital, Belgium. thibaut.vanzele@ugent.be

The Laryngoscope
|July 3, 2009
PubMed
Summary
This summary is machine-generated.

The complement system is activated in nasal secretions of patients with chronic rhinosinusitis with nasal polyps (CRSwNP), correlating with inflammation. This suggests its role in CRSwNP pathogenesis, contributing to edema and granulocytic inflammation.

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Published on: February 28, 2021

Area of Science:

  • Immunology
  • Otorhinolaryngology

Background:

  • Chronic rhinosinusitis with nasal polyps (CRSwNP) pathogenesis is not fully understood.
  • Bacterial colonization in CRSwNP suggests a role for innate immune mechanisms like the complement system.
  • Previous studies have limited investigation into the complement system's role in CRSwNP.

Purpose of the Study:

  • To investigate local and systemic complement system activation in CRSwNP.
  • To correlate complement activation with local/systemic eosinophilic and neutrophilic inflammation.
  • To assess the relationship between complement activation and local plasma exudation in CRSwNP.

Main Methods:

  • Quantified complement factors (C3a desArg, C5a desArg) and inflammatory markers (eosinophilic cationic protein, myeloperoxidase) in nasal secretions and serum.
  • Analyzed albumin and alpha2-macroglobulin for plasma exudation.
  • Used immunohistochemistry to detect the membrane attack complex (C5b9) in nasal tissue.

Main Results:

  • Significantly higher C3a desArg and C5a desArg concentrations were found in CRSwNP nasal secretions compared to controls.
  • Serum complement factor levels did not differ significantly between CRSwNP patients and controls.
  • C5a desArg in secretions correlated with eosinophil cationic protein, and C5b9 was deposited in CRSwNP nasal polyp tissue.

Conclusions:

  • The complement system is locally activated in CRSwNP.
  • Complement activation correlates with eosinophilic inflammation and plasma exudation in CRSwNP.
  • These findings support the complement system's involvement in CRSwNP pathogenesis, contributing to edema and inflammation.