Literature DB >> 21898142

Association of IRF5 polymorphisms with susceptibility to hemophagocytic lymphohistiocytosis in children.

Masakatsu Yanagimachi1, Hiroaki Goto, Takako Miyamae, Keisuke Kadota, Tomoyuki Imagawa, Masaaki Mori, Hidenori Sato, Ryu Yanagisawa, Tetsuji Kaneko, Satoshi Morita, Eiichi Ishii, Shumpei Yokota.   

Abstract

INTRODUCTION: Hemophagocytic lymphohistiocytosis (HLH) is a hyperinflammatory syndrome and has a varied genetic background. The polymorphism of interferon regulatory factor 5 gene (IRF5) was reported to be associated with susceptibility to macrophage activation syndrome. IRF5 acts as a master transcription factor in the activation of pro-inflammatory cytokines. We assessed associations of IRF5 gene polymorphisms with susceptibility to secondary HLH.
METHODS: Three IRF5 single nucleotide polymorphisms (rs729302, rs2004640, and rs2280714) were genotyped using TaqMan assays in 82 secondary HLH patients and 188 control subjects.
RESULTS: There was a significant association of the GT/TT genotype at rs2004640 with secondary HLH susceptibility (p < 0.01). The IRF5 haplotype (rs729302 A, rs2004640 T, and rs2280714 T) was associated with secondary HLH susceptibility (p < 0.01).
CONCLUSIONS: These findings indicate that IRF5 is a genetic factor influencing the susceptibility to secondary HLH and that the IRF5-associated immune response contributes to the pathogenesis of HLH.

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Year:  2011        PMID: 21898142     DOI: 10.1007/s10875-011-9583-x

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  38 in total

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Authors:  Jan-Inge Henter; Annacarin Horne; Maurizio Aricó; R Maarten Egeler; Alexandra H Filipovich; Shinsaku Imashuku; Stephan Ladisch; Ken McClain; David Webb; Jacek Winiarski; Gritta Janka
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Authors:  Robert R Graham; Sergey V Kozyrev; Emily C Baechler; M V Prasad Linga Reddy; Robert M Plenge; Jason W Bauer; Ward A Ortmann; Thearith Koeuth; Ma Francisca González Escribano; Bernardo Pons-Estel; Michelle Petri; Mark Daly; Peter K Gregersen; Javier Martín; David Altshuler; Timothy W Behrens; Marta E Alarcón-Riquelme
Journal:  Nat Genet       Date:  2006-04-16       Impact factor: 38.330

4.  Integral role of IRF-5 in the gene induction programme activated by Toll-like receptors.

Authors:  Akinori Takaoka; Hideyuki Yanai; Seiji Kondo; Gordon Duncan; Hideo Negishi; Tatsuaki Mizutani; Shin-Ichi Kano; Kenya Honda; Yusuke Ohba; Tak W Mak; Tadatsugu Taniguchi
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5.  Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.

Authors:  Udo zur Stadt; Susanne Schmidt; Brigitte Kasper; Karin Beutel; A Sarper Diler; Jan-Inge Henter; Hartmut Kabisch; Reinhard Schneppenheim; Peter Nürnberg; Gritta Janka; Hans Christian Hennies
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6.  Inflammatory cytokines in virus-associated hemophagocytic syndrome. Interferon-gamma as a sensitive indicator of disease activity.

Authors:  S Ohga; A Matsuzaki; M Nishizaki; T Nagashima; T Kai; M Suda; K Ueda
Journal:  Am J Pediatr Hematol Oncol       Date:  1993-08

Review 7.  Hemophagocytic syndromes.

Authors:  Gritta E Janka
Journal:  Blood Rev       Date:  2007-06-21       Impact factor: 8.250

8.  A single nucleotide polymorphism in the IRF5 promoter region is associated with susceptibility to rheumatoid arthritis in the Japanese population.

Authors:  K Shimane; Y Kochi; R Yamada; Y Okada; A Suzuki; A Miyatake; M Kubo; Y Nakamura; K Yamamoto
Journal:  Ann Rheum Dis       Date:  2008-04-13       Impact factor: 19.103

9.  Hemophagocytic lymphohistiocytosis is associated with deficiencies of cellular cytolysis but normal expression of transcripts relevant to killer-cell-induced apoptosis.

Authors:  E Marion Schneider; Ingrid Lorenz; Michaela Müller-Rosenberger; Gerald Steinbach; Martina Kron; Gritta E Janka-Schaub
Journal:  Blood       Date:  2002-10-15       Impact factor: 22.113

10.  Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11.

Authors:  Udo zur Stadt; Jan Rohr; Wenke Seifert; Florian Koch; Samantha Grieve; Julia Pagel; Julia Strauss; Brigitte Kasper; Gudrun Nürnberg; Christian Becker; Andrea Maul-Pavicic; Karin Beutel; Gritta Janka; Gillian Griffiths; Stephan Ehl; Hans Christian Hennies
Journal:  Am J Hum Genet       Date:  2009-10       Impact factor: 11.025

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Review 2.  [Still's disease in children and adults].

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Review 3.  The genetics of macrophage activation syndrome.

Authors:  Grant S Schulert; Randy Q Cron
Journal:  Genes Immun       Date:  2020-04-15       Impact factor: 2.676

4.  Clinical characteristics and genetic analysis of childhood acute lymphoblastic leukemia with hemophagocytic lymphohistiocytosis: a Japanese retrospective study by the Kyushu-Yamaguchi Children's Cancer Study Group.

Authors:  Hiroshi Moritake; Sachiyo Kamimura; Hiroyuki Nunoi; Hideki Nakayama; Aiko Suminoe; Hiroko Inada; Jiro Inagaki; Fumio Yanai; Yasuhiro Okamoto; Yuichi Shinkoda; Maiko Shimomura; Nobuyoshi Itonaga; Noriko Hotta; Yasufumi Hidaka; Osamu Ohara; Masakatsu Yanagimachi; Noriko Nakajima; Jun Okamura; Yoshifumi Kawano
Journal:  Int J Hematol       Date:  2014-05-15       Impact factor: 2.490

5.  Mangiferin inhibits macrophage classical activation via downregulating interferon regulatory factor 5 expression.

Authors:  Zhiquan Wei; Li Yan; Yixin Chen; Chuanhong Bao; Jing Deng; Jiagang Deng
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6.  Hemophagocytic lymphohistiocytosis is associated with Bartonella henselae infection in a patient with multiple susceptibility genes.

Authors:  Tianjun Yang; Qing Mei; Lei Zhang; Zhendong Chen; Chunyan Zhu; Xiaowei Fang; Shike Geng; Aijun Pan
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  6 in total

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