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Cellular and molecular basis of proximal small intestine disorders.
Bildstein, Tania; Charbit-Henrion, Fabienne; Azabdaftari, Aline; Cerf-Bensussan, Nadine; Uhlig, Holm H.
Affiliation
  • Bildstein T; Great Ormond Street Hospital for Children, Department of Paediatric Gastroenterology, London, UK.
  • Charbit-Henrion F; Department of Genomic Medicine for Rare Diseases, Necker-Enfants Malades Hospital, APHP, University of Paris-Cité, Paris, France.
  • Azabdaftari A; INSERM UMR1163, Intestinal Immunity, Institut Imagine, Paris, France.
  • Cerf-Bensussan N; Translational Gastroenterology Unit, Nuffield Department of Medicine, Oxford, UK.
  • Uhlig HH; INSERM UMR1163, Intestinal Immunity, Institut Imagine, Paris, France. nadine.cerf-bensussan@inserm.fr.
Nat Rev Gastroenterol Hepatol ; 21(10): 687-709, 2024 Oct.
Article in En | MEDLINE | ID: mdl-39117867
ABSTRACT
The proximal part of the small intestine, including duodenum and jejunum, is not only dedicated to nutrient digestion and absorption but is also a highly regulated immune site exposed to environmental factors. Host-protective responses against pathogens and tolerance to food antigens are essential functions in the small intestine. The cellular ecology and molecular pathways to maintain those functions are complex. Maladaptation is highlighted by common immune-mediated diseases such as coeliac disease, environmental enteric dysfunction or duodenal Crohn's disease. An expanding spectrum of more than 100 rare monogenic disorders inform on causative molecular mechanisms of nutrient absorption, epithelial homeostasis and barrier function, as well as inflammatory immune responses and immune regulation. Here, after summarizing the architectural and cellular traits that underlie the functions of the proximal intestine, we discuss how the integration of tissue immunopathology and molecular mechanisms can contribute towards our understanding of disease and guide diagnosis. We propose an integrated mechanism-based taxonomy and discuss the latest experimental approaches to gain new mechanistic insight into these disorders with large disease burden worldwide as well as implications for therapeutic interventions.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Celiac Disease / Intestine, Small Limits: Humans Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Main subject: Celiac Disease / Intestine, Small Limits: Humans Language: En Year: 2024 Type: Article