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ABSTRACT: Background
Patients with signal transducer and activator of transcription 5b (STAT5b) deficiency have impairment in T-cell homeostasis and natural killer (NK) cells which leads to autoimmunity, recurrent infections, and combined immune deficiency.Objective
In this study we characterized the NK cell defect in STAT5b-deficient human NK cells, as well as Stat5b-/- mice.Methods
We used multiparametric flow cytometry, functional NK cell assays, microscopy, and a Stat5b-/- mouse model to elucidate the effect of impaired and/or absent STAT5b on NK cell development and function.Results
This alteration generated a nonfunctional CD56bright NK cell subset characterized by low cytokine production. The CD56dim NK cell subset had decreased expression of perforin and CD16 and a greater frequency of cells expressing markers of immature NK cells. We observed low NK cell numbers and impaired NK cell maturation, suggesting that STAT5b is involved in terminal NK cell maturation in Stat5b-/- mice. Furthermore, human STAT5b-deficient NK cells had low cytolytic capacity, and fixed-cell microscopy showed poor convergence of lytic granules. This was accompanied by decreased expression of costimulatory and activating receptors. Interestingly, granule convergence and cytolytic function were restored after IL-2 stimulation.Conclusions
Our results show that in addition to the impaired terminal maturation of NK cells, human STAT5b mutation leads to impairments in early activation events in NK cell lytic synapse formation. Our data provide further insight into NK cell defects caused by STAT5b deficiency.
SUBMITTER: Vargas-Hernandez A
PROVIDER: S-EPMC7155380 | biostudies-literature | 2020 Jan
REPOSITORIES: biostudies-literature
The Journal of allergy and clinical immunology 20191007 1
<h4>Background</h4>Patients with signal transducer and activator of transcription 5b (STAT5b) deficiency have impairment in T-cell homeostasis and natural killer (NK) cells which leads to autoimmunity, recurrent infections, and combined immune deficiency.<h4>Objective</h4>In this study we characterized the NK cell defect in STAT5b-deficient human NK cells, as well as Stat5b<sup>-/-</sup> mice.<h4>Methods</h4>We used multiparametric flow cytometry, functional NK cell assays, microscopy, and a Sta ...[more]