Characterization of Canine Peyer's Patches by Multidimensional Analysis: Insights from Immunofluorescence, Flow Cytometry, and Single-Cell RNA Sequencing.

Q3 Medicine ImmunoHorizons Pub Date : 2023-11-01 DOI:10.4049/immunohorizons.2300091
Beatriz Miguelena Chamorro, Sodiq Ayobami Hameed, Marianne Dechelette, Jean-Baptiste Claude, Lauriane Piney, Ludivine Chapat, Gokul Swaminathan, Hervé Poulet, Stéphanie Longet, Karelle De Luca, Egbert Mundt, Stéphane Paul
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Abstract

The oral route is effective and convenient for vaccine administration to stimulate a protective immune response. GALT plays a crucial role in mucosal immune responses, with Peyer's patches (PPs) serving as the primary site of induction. A comprehensive understanding of the structures and functions of these structures is crucial for enhancing vaccination strategies and comprehending disease mechanisms; nonetheless, our current knowledge of these structures in dogs remains incomplete. We performed immunofluorescence and flow cytometry studies on canine PPs to identify cell populations and structures. We also performed single-cell RNA sequencing (scRNA-seq) to investigate the immune cell subpopulations present in PPs at steady state in dogs. We generated and validated an Ab specifically targeting canine M cells, which will be a valuable tool for elucidating Ag trafficking into the GALT of dogs. Our findings will pave the way for future studies of canine mucosal immune responses to oral vaccination and enteropathies. Moreover, they add to the growing body of knowledge in canine immunology, further expanding our understanding of the complex immune system of dogs.

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犬Peyer斑块的多维分析表征:来自免疫荧光、流式细胞术和单细胞RNA测序的见解。
口服途径是有效和方便的疫苗接种,以刺激保护性免疫反应。GALT在粘膜免疫应答中起着至关重要的作用,而Peyer’s patches (PPs)是主要的诱导位点。全面了解这些结构的结构和功能对于加强疫苗接种策略和理解疾病机制至关重要;尽管如此,我们目前对狗的这些结构的了解仍然不完整。我们对犬PPs进行了免疫荧光和流式细胞术研究,以确定细胞群和结构。我们还进行了单细胞RNA测序(scRNA-seq)来研究狗在稳定状态下PPs中存在的免疫细胞亚群。我们生成并验证了一种特异性靶向犬M细胞的抗体,这将为阐明Ag进入犬GALT提供有价值的工具。我们的发现将为进一步研究犬粘膜免疫应答对口服疫苗和肠病的反应铺平道路。此外,它们增加了犬类免疫学不断增长的知识体系,进一步扩大了我们对犬类复杂免疫系统的理解。
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CiteScore
3.70
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0.00%
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0
审稿时长
4 weeks
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