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An Slfn2 mutation causes lymphoid and myeloid immunodeficiency due to loss of immune cell quiescence.

Nature immunology | 2010

Here we describe a previously unknown form of inherited immunodeficiency revealed by an N-ethyl-N-nitrosourea-induced mutation called elektra. Mice homozygous for this mutation showed enhanced susceptibility to bacterial and viral infection and diminished numbers of T cells and inflammatory monocytes that failed to proliferate after infection and died via the intrinsic apoptotic pathway in response to diverse proliferative stimuli. They also had a greater proportion of T cells poised to replicate DNA, and their T cells expressed a subset of activation markers, suggestive of a semi-activated state. We positionally ascribe the elektra phenotype to a mutation in the gene encoding Schlafen-2 (Slfn2). Our findings identify a physiological role for Slfn2 in the defense against pathogens through the regulation of quiescence in T cells and monocytes.

Pubmed ID: 20190759 RIS Download

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Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: P01 AI070167-01
  • Agency: NIAID NIH HHS, United States
    Id: P01 AI070167
  • Agency: NIGMS NIH HHS, United States
    Id: R37 GM067759
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI076396
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR031203

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B6.MRL-Faslpr/J (tool)

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