Cytokine secretion and NK cell activity in human ADAM17 deficiency

被引:30
|
作者
Tsukerman, Pinchas [1 ]
Eisenstein, Eli M. [2 ]
Chavkin, Maor [2 ]
Schmiedel, Dominik [1 ]
Wong, Eitan [3 ]
Werner, Marion [4 ]
Yaacov, Barak [4 ]
Averbuch, Diana [5 ]
Molho-Pessach, Vered [6 ]
Stepensky, Polina [7 ]
Kaynan, Noa [1 ]
Bar-On, Yotam [1 ]
Seidel, Einat [1 ]
Yamin, Rachel [1 ]
Sagi, Irit [3 ]
Elpeleg, Orly [4 ]
Mandelboim, Ofer [1 ]
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, BioMed Res Inst, Lautenberg Ctr Gen & Tumor Immunol, IL-91010 Jerusalem, Israel
[2] Hadassah Hebrew Univ, Med Ctr, Dept Pediat, Mt Scopus, Jerusalem Il, Israel
[3] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
[4] Hadassah Hebrew Univ, Med Ctr, Monique & Jacques Roboh Dept Genet Res, Jerusalem, Israel
[5] Hadassah Hebrew Univ, Med Ctr, Pediat Infect Dis Unit, Jerusalem, Israel
[6] Hadassah Hebrew Univ, Med Ctr, Dept Dermatol, Jerusalem, Israel
[7] Hadassah Hebrew Univ, Med Ctr, Pediat Hematooncol & Bone Marrow Transplantat Dep, Jerusalem, Israel
基金
欧洲研究理事会; 以色列科学基金会;
关键词
ADAM17; deficiency; NK cells; CD16; ADCC; Immunology and Microbiology Section; Immune response; Immunity; NATURAL-KILLER-CELLS; CD16; CYTOTOXICITY; INHIBITION; RECEPTORS; INFLAMMATION; ACTIVATION; FC; REGENERATION; STIMULATION;
D O I
10.18632/oncotarget.6629
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Genetic deficiencies provide insights into gene function in humans. Here we describe a patient with a very rare genetic deficiency of ADAM17. We show that the patient's PBMCs had impaired cytokine secretion in response to LPS stimulation, correlating with the clinical picture of severe bacteremia from which the patient suffered. ADAM17 was shown to cleave CD16, a major NK killer receptor. Functional analysis of patient's NK cells demonstrated that his NK cells express normal levels of activating receptors and maintain high surface levels of CD16 following mAb stimulation. Activation of individual NK cell receptors showed that the patient's NK cells are more potent when activated directly by CD16, albeit no difference was observed in Antibody Depedent Cytotoxicity (ADCC) assays. Our data suggest that ADAM17 inhibitors currently considered for clinical use to boost CD16 activity should be cautiously applied, as they might have severe side effects resulting from impaired cytokine secretion.
引用
收藏
页码:44151 / 44160
页数:10
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