Inflammatory skin and bowel disease linked to ADAM17 deletion.

نویسندگان

  • Diana C Blaydon
  • Paolo Biancheri
  • Wei-Li Di
  • Vincent Plagnol
  • Rita M Cabral
  • Matthew A Brooke
  • David A van Heel
  • Franz Ruschendorf
  • Mark Toynbee
  • Amanda Walne
  • Edel A O'Toole
  • Joanne E Martin
  • Keith Lindley
  • Tom Vulliamy
  • Dominic J Abrams
  • Thomas T MacDonald
  • John I Harper
  • David P Kelsell
چکیده

We performed genetic and immunohistochemical studies in a sister and brother with autosomal recessive neonatal inflammatory skin and bowel lesions. The girl died suddenly at 12 years of age from parvovirus B19-associated myocarditis; her brother had mild cardiomyopathy. We identified a loss-of-function mutation in ADAM17, which encodes a disintegrin and metalloproteinase 17 (also called tumor necrosis factor α [TNF-α]-converting enzyme, or TACE), as the probable cause of this syndrome. Peripheral-blood mononuclear cells (PBMCs) obtained from the brother at 17 years of age showed high levels of lipopolysaccharide-induced production of interleukin-1β and interleukin-6 but impaired release of TNF-α. Despite repeated skin infections, this young man has led a relatively normal life. (Funded by Barts and the London Charity and the European Commission Seventh Framework Programme.).

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عنوان ژورنال:
  • The New England journal of medicine

دوره 365 16  شماره 

صفحات  -

تاریخ انتشار 2011