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The 423Q polymorphism of the X‐linked inhibitor of apoptosis gene influences monocyte function and is associated with periodic fever

2009; Wiley; Volume: 60; Issue: 11 Linguagem: Inglês

10.1002/art.24905

1529-0131

Massimo Ferretti, Marco Gattorno, Annalisa Chiocchetti, Riccardo Mesturini, Elisabetta Orilieri, Thea Bensi, Maria Pia Sormani, Giuseppe Cappellano, Elisa Cerutti, Stefania Nicola, A. Biava, Claudio Bardelli, Silvia Federici, Isabella Ceccherini, Maurizia Baldi, Claudio Santoro, Irma Dianzani, Alberto Martini, Umberto Dianzani,

Cancer-related molecular mechanisms research

Abstract Objective Hereditary periodic fever syndromes (HPFs) develop as a result of uncontrolled activation of the inflammatory response, with a substantial contribution from interleukin‐1β or tumor necrosis factor α (TNFα). The HPFs include familial Mediterranean fever (FMF), hyperimmunoglobulinemia D with periodic fever syndrome (HIDS), TNF receptor–associated syndrome (TRAPS), and cryopyrinopathies, which are attributable to mutations of the MEFV , MVK , TNFRSF1A , and CIAS1 genes, respectively. However, in many patients, the mutated gene has not been determined; therefore, the condition in these patients with an HPF‐like clinical picture is referred to as idiopathic periodic fever (IPF). The aim of this study was to assess involvement of X‐linked inhibitor of apoptosis (XIAP), which plays a role in caspase inhibition and NF‐κB signaling, both of which are processes that influence the development of inflammatory cells. Methods The XIAP gene (X‐linked) was sequenced in 87 patients with IPF, 46 patients with HPF (13 with HIDS, 17 with TRAPS, and 16 with FMF), and 182 healthy control subjects. The expression of different alleles was evaluated by sequencing XIAP ‐specific complementary DNA mini‐libraries and by real‐time polymerase chain reaction and Western blot analyses. The functional effect of XIAP on caspase 9 activity was assessed by a fluorimetric assay, and cytokine secretion was evaluated by enzyme‐linked immunosorbent assay. Results Sequencing disclosed a 1268A>C variation that caused a Q423P amino acid substitution. The frequency of 423Q‐homozygous female patients and 423Q‐hemizygous male patients was significantly higher in the IPF group than in the control group (69% versus 51%; odds ratio 2.17, 95% confidence interval 1.23–3.87, P = 0.007), whereas no significant difference was detected in the HPF group (59%) compared with controls. In primary lymphocytes and transfected cell lines, 423Q, as compared with 423P, was associated with higher XIAP protein and messenger RNA expression and lower caspase 9 activation. In lipopolysaccharide‐activated monocytes, 423Q was associated with higher secretion of TNFα. Conclusion These results suggest that 423Q is a predisposing factor for IPF development, possibly through its influence on monocyte function.