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


Journal

Inflammatory bowel diseases
ISSN: 1536-4844
Titre abrégé: Inflamm Bowel Dis
Pays: England
ID NLM: 9508162

Informations de publication

Date de publication:
01 02 2023
Historique:
received: 11 08 2022
pubmed: 8 10 2022
medline: 3 2 2023
entrez: 7 10 2022
Statut: ppublish

Résumé

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. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 36206201
pii: 6752324
doi: 10.1093/ibd/izac201
pmc: PMC9890215
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

274-285

Subventions

Organisme : NIDDK NIH HHS
ID : T32 DK108735
Pays : United States
Organisme : NIH HHS
ID : P51 OD011132
Pays : United States
Organisme : NIH HHS
ID : S10 OD026799
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2022 Crohn’s & Colitis Foundation. Published by Oxford University Press on behalf of Crohn’s & Colitis Foundation.

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Auteurs

Sushma Chowdary Maddipatla (SC)

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

Vasantha L Kolachala (VL)

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

Suresh Venkateswaran (S)

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

Anne F Dodd (AF)

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

Ranjit Singh Pelia (RS)

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

Duke Geem (D)

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

Hong Yin (H)

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

Yutong Sun (Y)

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

Congmin Xu (C)

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

Angela Mo (A)

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

Astrid Kosters (A)

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

Junkai Yang (J)

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

Jason D Matthews (JD)

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

Eliver Ghosn (E)

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

Subra Kugathasan (S)

Division of Pediatric Gastroenterology, Department of Pediatrics and Pediatric Research Institute, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.
Genetics and Molecular Biology Program, Emory University School of Medicine, Atlanta, GA, USAand.
Department of Human Genetics, Emory University, Atlanta, GA, USA.

Peng Qiu (P)

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

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