Ontology highlight
ABSTRACT:
SUBMITTER: Rigoni R
PROVIDER: S-EPMC4813669 | biostudies-literature | 2016 Mar
REPOSITORIES: biostudies-literature
Rigoni Rosita R Fontana Elena E Guglielmetti Simone S Fosso Bruno B D'Erchia Anna Maria AM Maina Virginia V Taverniti Valentina V Castiello Maria Carmina MC Mantero Stefano S Pacchiana Giovanni G Musio Silvia S Pedotti Rosetta R Selmi Carlo C Mora J Rodrigo JR Pesole Graziano G Vezzoni Paolo P Poliani Pietro Luigi PL Grassi Fabio F Villa Anna A Cassani Barbara B
The Journal of experimental medicine 20160229 3
Omenn syndrome (OS) is caused by hypomorphic Rag mutations and characterized by a profound immunodeficiency associated with autoimmune-like manifestations. Both in humans and mice, OS is mediated by oligoclonal activated T and B cells. The role of microbial signals in disease pathogenesis is debated. Here, we show that Rag2(R229Q) knock-in mice developed an inflammatory bowel disease affecting both the small bowel and colon. Lymphocytes were sufficient for disease induction, as intestinal CD4 T ...[more]