Assessing Cellular and Transcriptional Diversity of Ileal Mucosa Among Treatment-Naïve and Treated Crohn’s Disease

Author:

Maddipatla Sushma Chowdary1,Kolachala Vasantha L1,Venkateswaran Suresh1,Dodd Anne F1,Pelia Ranjit Singh1,Geem Duke1,Yin Hong2,Sun Yutong3,Xu Congmin4,Mo Angela5,Kosters Astrid6,Yang Junkai6,Matthews Jason D1,Ghosn Eliver7,Kugathasan Subra189ORCID,Qiu Peng4

Affiliation:

1. Division of Pediatric Gastroenterology, Department of Pediatrics and Pediatric Research Institute, Children’s Healthcare of Atlanta, Emory University School of Medicine , Atlanta, GA , USA

2. Department of Pathology, Children’s Healthcare of Atlanta, Emory University , Atlanta, GA , USA

3. School of Electrical and Computer Engineering, Georgia Institute of Technology , Atlanta, GA , USA

4. Department of Biomedical Engineering, Georgia Institute of Technology and Emory University , Atlanta, GA , USA

5. School of Biological Sciences, Georgia Institute of Technology , Atlanta, GA , USA

6. Lowance Center for Human Immunology, Division of Immunology and Rheumatology, Department of Medicine, Emory University School of Medicine , Atlanta, GA , USA

7. Emory Vaccine Center, Lowance Center for Human Immunology, Departments of Medicine and Pediatrics, Emory University School of Medicine , Atlanta, GA , USA

8. Genetics and Molecular Biology Program, Emory University School of Medicine , Atlanta, GA , USA and

9. Department of Human Genetics, Emory University , Atlanta, GA , USA

Abstract

Abstract Background Crohn’s disease is a lifelong disease characterized by chronic inflammation of the gastrointestinal tract. Defining the cellular and transcriptional composition of the mucosa at different stages of disease progression is needed for personalized therapy in Crohn’s. Methods Ileal biopsies were obtained from (1) control subjects (n = 6), (2) treatment-naïve patients (n = 7), and (3) established (n = 14) Crohn’s patients along with remission (n = 3) and refractory (n = 11) treatment groups. The biopsies processed using 10x Genomics single cell 5' yielded 139 906 cells. Gene expression count matrices of all samples were analyzed by reciprocal principal component integration, followed by clustering analysis. Manual annotations of the clusters were performed using canonical gene markers. Cell type proportions, differential expression analysis, and gene ontology enrichment were carried out for each cell type. Results We identified 3 cellular compartments with 9 epithelial, 1 stromal, and 5 immune cell subtypes. We observed differences in the cellular composition between control, treatment-naïve, and established groups, with the significant changes in the epithelial subtypes of the treatment-naïve patients, including microfold, tuft, goblet, enterocyte,s and BEST4+ cells. Surprisingly, fewer changes in the composition of the immune compartment were observed; however, gene expression in the epithelial and immune compartment was different between Crohn’s phenotypes, indicating changes in cellular activity. Conclusions Our study identified cellular and transcriptional signatures associated with treatment-naïve Crohn’s disease that collectively point to dysfunction of the intestinal barrier with an increase in inflammatory cellular activity. Our analysis also highlights the heterogeneity among patients within the same disease phenotype, shining a new light on personalized treatment responses and strategies.

Funder

Leona M. and Harry B. Helmsley Charitable Trust

National Science Foundation

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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