X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production

نویسندگان

  • Orchidée Filipe-Santos
  • Jacinta Bustamante
  • Margje H. Haverkamp
  • Emilie Vinolo
  • Cheng-Lung Ku
  • Anne Puel
  • David M. Frucht
  • Karin Christel
  • Horst von Bernuth
  • Emmanuelle Jouanguy
  • Jacqueline Feinberg
  • Anne Durandy
  • Brigitte Senechal
  • Ariane Chapgier
  • Guillaume Vogt
  • Ludovic de Beaucoudrey
  • Claire Fieschi
  • Capucine Picard
  • Meriem Garfa
  • Jalel Chemli
  • Mohamed Bejaoui
  • Maria N. Tsolia
  • Necil Kutukculer
  • Alessandro Plebani
  • Luigi Notarangelo
  • Christine Bodemer
  • Frédéric Geissmann
  • Alain Israël
  • Michel Véron
  • Maike Knackstedt
  • Ridha Barbouche
  • Laurent Abel
  • Klaus Magdorf
  • Dominique Gendrel
  • Fabrice Agou
  • Steven M. Holland
  • Jean-Laurent Casanova
چکیده

Germline mutations in five autosomal genes involved in interleukin (IL)-12-dependent, interferon (IFN)-gamma-mediated immunity cause Mendelian susceptibility to mycobacterial diseases (MSMD). The molecular basis of X-linked recessive (XR)-MSMD remains unknown. We report here mutations in the leucine zipper (LZ) domain of the NF-kappaB essential modulator (NEMO) gene in three unrelated kindreds with XR-MSMD. The mutant proteins were produced in normal amounts in blood and fibroblastic cells. However, the patients' monocytes presented an intrinsic defect in T cell-dependent IL-12 production, resulting in defective IFN-gamma secretion by T cells. IL-12 production was also impaired as the result of a specific defect in NEMO- and NF-kappaB/c-Rel-mediated CD40 signaling after the stimulation of monocytes and dendritic cells by CD40L-expressing T cells and fibroblasts, respectively. However, the CD40-dependent up-regulation of costimulatory molecules of dendritic cells and the proliferation and immunoglobulin class switch of B cells were normal. Moreover, the patients' blood and fibroblastic cells responded to other NF-kappaB activators, such as tumor necrosis factor-alpha, IL-1beta, and lipopolysaccharide. These two mutations in the NEMO LZ domain provide the first genetic etiology of XR-MSMD. They also demonstrate the importance of the T cell- and CD40L-triggered, CD40-, and NEMO/NF-kappaB/c-Rel-mediated induction of IL-12 by monocyte-derived cells for protective immunity to mycobacteria in humans.

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عنوان ژورنال:
  • The Journal of Experimental Medicine

دوره 203  شماره 

صفحات  -

تاریخ انتشار 2006