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10.4049/jimmunol.1501284

http://scihub22266oqcxt.onion/10.4049/jimmunol.1501284
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C4779709!4779709!26880764
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suck abstract from ncbi


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pmid26880764      J+Immunol 2016 ; 196 (6): 2492-503
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  • A Heterozygous RAB27A Mutation Associated with Delayed Cytolytic Granule Polarization and Hemophagocytic Lymphohistiocytosis1 #MMPMID26880764
  • Zhang M; Bracaglia C; Prencipe G; Bemrich-Stolz CJ; Beukelman T; Dimmitt RA; Chatham WW; Zhang K; Li H; Walter MR; De Benedetti F; Grom AA; Cron RQ
  • J Immunol 2016[Mar]; 196 (6): 2492-503 PMID26880764show ga
  • Frequently fatal, primary hemophagocytic lymphohistiocytosis (HLH) occurs in infancy resulting from homozygous mutations in natural killer (NK) and CD8 T cell cytolytic pathway genes. Secondary HLH presents after infancy and may be associated with heterozygous mutations in HLH genes. We report 2 unrelated teenagers with HLH and an identical heterozygous RAB27A mutation (c.259G>C). We explore the contribution of this Rab27A missense (p.A87P) mutation on NK cell cytolytic function by cloning it into a lentiviral expression vector prior to introduction into the human NK-92 cell line. NK cell degranulation (CD107a expression), target cell conjugation, and K562 target cell lysis was compared between mutant and wild-type transduced NK-92 cells. Polarization of granzyme B to the immunologic synapse and interaction of mutant Rab27A (p.A87P) with Munc13-4 were explored by confocal microscopy and proximity ligation assay, respectively. Over-expression of the RAB27A mutation had no effect on cell conjugate formation between the NK and target cells but decreased NK cell cytolytic activity and degranulation. Moreover, the mutant Rab27A protein decreased binding to Munc13-4 and delayed granzyme B polarization towards the immunologic synapse. This heterozygous RAB27A mutation blurs the genetic distinction between primary and secondary HLH by contributing to HLH via a partial dominant-negative effect.
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