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Immunodeficiency and autoimmune enterocolopathy linked to NFAT5 haploinsufficiency.
Boland, Brigid S; Widjaja, Christella E; Banno, Asoka; Zhang, Bing; Kim, Stephanie H; Stoven, Samantha; Peterson, Michael R; Jones, Marilyn C; Su, H Irene; Crowe, Sheila E; Bui, Jack D; Ho, Samuel B; Okugawa, Yoshinaga; Goel, Ajay; Marietta, Eric V; Khosroheidari, Mahdieh; Jepsen, Kristen; Aramburu, Jose; López-Rodríguez, Cristina; Sandborn, William J; Murray, Joseph A; Harismendy, Olivier; Chang, John T.
Affiliation
  • Boland BS; Department of Medicine, University of California San Diego, La Jolla, CA 92093; Inflammatory Bowel Disease Center, University of California San Diego, La Jolla, CA 92093;
  • Widjaja CE; Department of Medicine, University of California San Diego, La Jolla, CA 92093;
  • Banno A; Department of Medicine, University of California San Diego, La Jolla, CA 92093;
  • Zhang B; Department of Medicine, University of California San Diego, La Jolla, CA 92093;
  • Kim SH; Department of Medicine, University of California San Diego, La Jolla, CA 92093;
  • Stoven S; Department of Medicine, Mayo Clinic, Rochester, MN 55905;
  • Peterson MR; Western Washington Pathology and Multicare Health System, Tacoma, WA 98405;
  • Jones MC; Department of Pediatrics and Rady Children's Hospital, University of California San Diego, La Jolla, CA 92093;
  • Su HI; Department of Reproductive Medicine, University of California San Diego, La Jolla, CA 92093;
  • Crowe SE; Department of Medicine, University of California San Diego, La Jolla, CA 92093;
  • Bui JD; Department of Pathology, University of California San Diego, La Jolla, CA 92093;
  • Ho SB; Department of Pathology, University of California San Diego, La Jolla, CA 92093;
  • Okugawa Y; Center for Gastrointestinal Research, Center for Epigenetics, Cancer Prevention and Cancer Genomics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX 75246; Charles A. Sammons Cancer Center, Baylor University Medical Center, Dallas, TX 75246;
  • Goel A; Center for Gastrointestinal Research, Center for Epigenetics, Cancer Prevention and Cancer Genomics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX 75246; Charles A. Sammons Cancer Center, Baylor University Medical Center, Dallas, TX 75246;
  • Marietta EV; Department of Medicine, Mayo Clinic, Rochester, MN 55905;
  • Khosroheidari M; Institute of Genomic Medicine, University of California San Diego, La Jolla, CA 92093;
  • Jepsen K; Institute of Genomic Medicine, University of California San Diego, La Jolla, CA 92093;
  • Aramburu J; Immunology Unit, Department of Experimental and Health Sciences, Pompeu Fabra University, Barcelona 08003 Spain; and.
  • López-Rodríguez C; Immunology Unit, Department of Experimental and Health Sciences, Pompeu Fabra University, Barcelona 08003 Spain; and.
  • Sandborn WJ; Department of Medicine, University of California San Diego, La Jolla, CA 92093; Inflammatory Bowel Disease Center, University of California San Diego, La Jolla, CA 92093;
  • Murray JA; Department of Medicine, Mayo Clinic, Rochester, MN 55905;
  • Harismendy O; Department of Medicine, University of California San Diego, La Jolla, CA 92093; Moores Cancer Center, University of California San Diego, La Jolla, CA 92093.
  • Chang JT; Department of Medicine, University of California San Diego, La Jolla, CA 92093; Inflammatory Bowel Disease Center, University of California San Diego, La Jolla, CA 92093; changj@ucsd.edu.
J Immunol ; 194(6): 2551-60, 2015 Mar 15.
Article de En | MEDLINE | ID: mdl-25667416
ABSTRACT
The link between autoimmune diseases and primary immunodeficiency syndromes has been increasingly appreciated. Immunologic evaluation of a young man with autoimmune enterocolopathy and unexplained infections revealed evidence of immunodeficiency, including IgG subclass deficiency, impaired Ag-induced lymphocyte proliferation, reduced cytokine production by CD8(+) T lymphocytes, and decreased numbers of NK cells. Genetic evaluation identified haploinsufficiency of NFAT5, a transcription factor regulating immune cell function and cellular adaptation to hyperosmotic stress, as a possible cause of this syndrome. Inhibition or deletion of NFAT5 in normal human and murine cells recapitulated several of the immune deficits identified in the patient. These results provide evidence of a primary immunodeficiency disorder associated with organ-specific autoimmunity linked to NFAT5 deficiency.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies auto-immunes / Facteurs de transcription / Haploinsuffisance / Maladies gastro-intestinales / Déficits immunitaires Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Adult / Animals / Humans / Male Langue: En Journal: J Immunol Année: 2015 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Maladies auto-immunes / Facteurs de transcription / Haploinsuffisance / Maladies gastro-intestinales / Déficits immunitaires Type d'étude: Diagnostic_studies / Prognostic_studies Limites: Adult / Animals / Humans / Male Langue: En Journal: J Immunol Année: 2015 Type de document: Article