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Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
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Systemic hypereosinophilic syndromes: when autoimmunity is Th2 mediated
Andrea Matucci1, Francesca Nencini1, Enrico Maggi2
1Immunoallergology Unit, AOU Careggi, University of Florence, Florence.
Current Opinion in Allergy and Clinical Immunology
|January 28, 2020
Summary
Hypereosinophilia involves Th2 cells and pathogenic autoantibodies in autoimmune diseases. Understanding these mechanisms, including innate lymphoid cells, guides new biologic therapies for hypereosinophilic syndrome.
Area of Science:
- Immunology
- Autoimmune Diseases
- Allergy and Asthma
Background:
- Hypereosinophilia presents diverse clinical conditions with significant epidemiological impact.
- Autoimmune diseases can involve Th2 cell responses, including eosinophilic conditions like eosinophilic granulomatosis with polyangiitis.
Purpose of the Study:
- To review the role of Th2 cells and autoimmune mechanisms in hypereosinophilia.
- To explore the involvement of innate lymphoid cells and Th1/Th17 cells in hypereosinophilic syndrome pathogenesis.
Main Methods:
- Review of recent evidence on pathogenic autoantibodies against eosinophil proteins.
- Analysis of cellular and molecular mechanisms in hypereosinophilic syndrome.
Main Results:
- Pathogenic autoantibodies against eosinophil proteins are implicated in severe asthma and eosinophilic vasculitis.
- Type 2 innate lymphoid cells and Th1/Th17 cells are central to hypereosinophilic syndrome pathogenesis.
Conclusions:
- Understanding the cellular and molecular pathways of hypereosinophilic syndrome is crucial.
- Targeting specific cytokines and factors involved in pathogenesis enables new biologic therapies.
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