A role for interleukin-12/23 in the maturation of human natural killer and CD56(+) T cells in vivo


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Guia S., Cognet C., de Beaucoudrey L., Tessmer M. S. , Jouanguy E., Berger C., ...Daha Fazla

BLOOD, cilt.111, ss.5008-5016, 2008 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 111 Konu: 10
  • Basım Tarihi: 2008
  • Doi Numarası: 10.1182/blood-2007-11-122259
  • Dergi Adı: BLOOD
  • Sayfa Sayıları: ss.5008-5016

Özet

Natural killer (NK) cells have been originally defined by their "naturally occurring" effector function. However, only a fraction of human NK cells is reactive toward a panel of prototypical tumor cell targets in vitro, both for the production of interferon-gamma (IFN-gamma) and for their cytotoxic response. In patients with IL12RB1 mutations that lead to a complete IL-12R beta 1 deficiency, the size of this naturally reactive NK cell subset is diminished, in particular for the IFN-gamma production. Similardata were obtained from a patient with a complete deficit in IL-12p40. In addition, the size of the subset of effector memory T cells expressing CD56 was severely decreased in IL-12R beta 1- and IL-12p40-deficient patients. Human NK cells thus require in vivo priming with IL-12/23 to acquire their full spectrum of functional reactivity, while T cells are dependent upon IL-12/23 signals for the differentiation and/or the maintenance of CD56(+) effector memory T cells. The susceptibility of IL-12/23 axis-deficient patients to Mycobacterium and Salmonella infections in combination with the absence of mycobacteriosis or salmonellosis in the rare cases of human NK cell deficiencies point to a role for CD56(+) T cells in the control of these infections in humans.