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The Schistosoma Granuloma: Friend or Foe?
- Source :
- Frontiers in Immunology, Frontiers in Immunology, Vol 4 (2013)
- Publication Year :
- 2013
- Publisher :
- Frontiers Media SA, 2013.
-
Abstract
- Infection of man with Schistosoma species of trematode parasite causes marked chronic morbidity. Individuals that become infected with Schistosomes may develop a spectrum of pathology ranging from mild cercarial dermatitis to severe tissue inflammation, in particular within the liver and intestines, which can lead to life threatening hepatosplenomegaly. It is well established that the etiopathology during schistosomiasis is primarily due to an excessive or unregulated inflammatory response to the parasite, in particular to eggs that become trapped in various tissue. The eggs forms the foci of a classical type 2 granulomatous inflammation, characterized by an eosinophil rich, CD4+ T helper (Th) 2 cell dominated infiltrate with additional infiltration of alternatively activated macrophages (M2). Indeed the sequela of the type 2 perioval granuloma is marked fibroblast infiltration and development of fibrosis. Paradoxically, while the granuloma is the cause of pathology it also can afford some protection, whereby the granuloma minimizes collateral tissue damage in the liver and intestines. Furthermore, the parasite is exquisitely reliant on the host to mount a granulomatous reaction to the eggs as this inflammatory response facilitates the successful excretion of the eggs from the host. In this focused review we will address the conundrum of the S. mansoni granuloma acting as both friend and foe in inflammation during infection.
- Subjects :
- lcsh:Immunologic diseases. Allergy
Pathology
medicine.medical_specialty
Fibrosi
Immunology
Cercarial Dermatitis
Inflammation
Schistosomiasis
Review Article
Biology
Fibrosis
medicine
Immunology and Allergy
granuloma
Schistosoma
fibrosis
Schistosoma mansoni
medicine.disease
biology.organism_classification
inflammation
Granuloma
medicine.symptom
lcsh:RC581-607
Infiltration (medical)
Subjects
Details
- ISSN :
- 16643224
- Volume :
- 4
- Database :
- OpenAIRE
- Journal :
- Frontiers in Immunology
- Accession number :
- edsair.doi.dedup.....e563f03a0613234fca24cf2fba9fd58b
- Full Text :
- https://doi.org/10.3389/fimmu.2013.00089