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Heterogeneity of Intestinal Tissue Eosinophils: Potential Considerations for Next-Generation Eosinophil-Targeting Strategies

Journal

CELLS
Volume 10, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/cells10020426

Keywords

eosinophil; eosinophilic gastrointestinal diseases; biologics; eosinophil sub-phenotypes

Categories

Funding

  1. Science Foundation Ireland [17/FRL/4863]
  2. N.I.H. [K23DK109263, R01AI121186]

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Eosinophils play crucial roles in gastrointestinal diseases, with diverse functional sub-phenotypes shaped by environmental pressures impacting disease outcomes. Understanding and targeting these sub-phenotypes may be key in developing next-generation treatments for inflammatory eosinophil functions while maintaining homeostatic roles.
Eosinophils are implicated in the pathophysiology of a spectrum of eosinophil-associated diseases, including gastrointestinal eosinophilic diseases (EGIDs). Biologics that target the IL-5 pathway and are intended to ablate eosinophils have proved beneficial in severe eosinophilic asthma and may offer promise in treating some endotypes of EGIDs. However, destructive effector functions of eosinophils are only one side of the coin; eosinophils also play important roles in immune and tissue homeostasis. A growing body of data suggest tissue eosinophils represent a plastic and heterogeneous population of functional sub-phenotypes, shaped by environmental (systemic and local) pressures, which may differentially impact disease outcomes. This may be particularly relevant to the GI tract, wherein the highest density of eosinophils reside in the steady state, resident immune cells are exposed to an especially broad range of external and internal environmental pressures, and greater eosinophil longevity may uniquely enrich for co-expression of eosinophil sub-phenotypes. Here we review the growing evidence for functional sub-phenotypes of intestinal tissue eosinophils, with emphasis on the multifactorial pressures that shape and diversify eosinophil identity and potential targets to inform next-generation eosinophil-targeting strategies designed to restrain inflammatory eosinophil functions while sustaining homeostatic roles.

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