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The intestine harbors a large population of resident eosinophils, yet the function of intestinal eosinophils has not been explored. Flow cytometry and whole-mount imaging identified eosinophils residing in the lamina propria along the length of the intestine prior to postnatal microbial colonization. Microscopy, transcriptomic analysis, and mass spectrometry of intestinal tissue revealed villus blunting, altered extracellular matrix, decreased epithelial cell turnover, increased gastrointestinal motility, and decreased lipid absorption in eosinophil-deficient mice. Mechanistically, intestinal epithelial cells released IL-33 in a microbiota-dependent manner, which led to eosinophil activation. The colonization of germ-free mice demonstrated that eosinophil activation in response to microbes regulated villous size alterations, macrophage maturation, epithelial barrier integrity, and intestinal transit. Collectively, our findings demonstrate a critical role for eosinophils in facilitating the mutualistic interactions between the host and microbiota and provide a rationale for the functional significance of their early life recruitment in the small intestine.
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http://dx.doi.org/10.1016/j.immuni.2022.05.014 | DOI Listing |
J Immunol
August 2025
Department of Internal Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander University Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.
Although alternatively-activated macrophages (AAM) have been implicated in the resolution of inflammation and tissue repair, their exact role, heterogeneity and origin in vivo remain incompletely defined. Here we show that distinct subsets of macrophages can acquire alternatively activated phenotypes in response to tissue injury where these cellular subsets display contrasting spatiotemporal dynamics and differentially contribute to the resolution of inflammation and tissue repair. By studying a model of cardiotoxin-induced muscle injury, we identify a population of monocyte-derived AAM characterized by expression of arginase-1 (Arg-1) and triggering receptor expressed on myeloid cells 2 (Trem2) that emerged in response to injury and fostered clearance of dying neutrophils and necrotic myofibers as well as the subsequent resolution of inflammation.
View Article and Find Full Text PDFMed
August 2025
Department of Experimental Medicine, University of Campania Luigi Vanvitelli, Naples, Italy.
Mepolizumab reduces exacerbations in eosinophilic COPD but shows limited effects on symptoms, lung function, or quality of life. The MATINEE trial supports a precision medicine approach targeting high blood eosinophil counts. However, IL-5 blockade alone may be insufficient due to complex, overlapping inflammatory pathways and persistent lung-resident eosinophils.
View Article and Find Full Text PDFCureus
July 2025
Department of Otolaryngology - Head and Neck Surgery, Dubai Health - MBRU, Dubai, ARE.
Objective Chronic rhinosinusitis with nasal polyposis (CRSwNP) is prevalent worldwide, but regional variations in disease endotypes have been described. The Gulf region is unique in genetic background and environmental conditions, potentially influencing disease characteristics. This study aimed to compare phenotypic traits and serum biomarkers associated with type 2 disease between CRSwNP patients in the Gulf and Canada.
View Article and Find Full Text PDFbioRxiv
July 2025
Divison of Allergy and Immunology, Department of Medicine, University of California San Diego, La Jolla, CA.
Group 2 innate lymphoid cells (ILC2s) are critical players during type 2 inflammation present in most forms of asthma. ILC2s are tissue-resident cells that produce cytokines IL-5 and IL-13 critical to eosinophilic airway inflammation, mucus production, remodeling, and hyperresponsiveness. Though each ILC subset (ILC1s, ILC2s, ILC3s) is identified by specific transcription factors, cell surface receptors and cytokine profiles, functional plasticity between ILC subtypes occurs in various contexts.
View Article and Find Full Text PDFJ Rhinol
July 2025
Department of Otorhinolaryngology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Background And Objectives: Chronic rhinosinusitis (CRS) is a heterogeneous inflammatory disease, classified into eosinophilic and non-eosinophilic subtypes. Although CD4+ tissue-resident memory T (TRM) cells play diverse roles in tissue homeostasis, their phenotypic and functional characteristics in the nasal tissue of patients with eosinophilic CRS (ECRS) remain poorly defined.
Methods: Nasal polyp tissue and/or peripheral blood (PB) samples were obtained from patients with ECRS undergoing endoscopic sinus surgery.