Wolcott-Rallison syndrome – crosstalk between PERK- EIF2A and type II interferon signaling

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY
Megha Konduri , Devin Boe , Nada Yazigi , Khalid Khan , Brant R. Ward , Blachy Davila Saldana , Douglas Cavener , Bhaskar Kallakury , Alexander Kroemer , Cal Matsumoto , Thomas Fishbein , Udeme D. Ekong
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引用次数: 0

Abstract

Immune activation is not reported in children with Wolcott-Rallison syndrome (WRS). We observed a pattern of immune activation pre-transplant in three children with WRS that was consistent with increased interferon-γ (IFN-γ) and its regulated chemokine, CXCL9 in plasma, and bone marrow that demonstrated scattered hemophagocytosis. One child developed hemophagocytic lymphohistiocytosis after liver transplantation that was fatal. Children with WRS should undergo evaluation for inflammatory biomarkers before transplant to aid in diagnosis of and prompt treatment of hyperinflammatory syndromes. Early recognition can prevent fatal outcomes.
Wolcott-Rallison综合征- PERK- EIF2A与II型干扰素信号之间的串扰。
免疫激活在Wolcott-Rallison综合征(WRS)儿童中未见报道。我们观察到三名患有WRS的儿童移植前的免疫激活模式,与血浆和骨髓中干扰素-γ (IFN-γ)及其调节的趋化因子CXCL9的增加一致,并表现出分散的噬血细胞现象。一名儿童在肝移植后出现噬血细胞性淋巴组织细胞增多症,死亡。患有WRS的儿童在移植前应接受炎症生物标志物评估,以帮助诊断和及时治疗高炎症综合征。早期识别可以防止致命的后果。
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来源期刊
CiteScore
4.10
自引率
0.00%
发文量
193
审稿时长
66 days
期刊介绍: The European Journal of Medical Genetics (EJMG) is a peer-reviewed journal that publishes articles in English on various aspects of human and medical genetics and of the genetics of experimental models. Original clinical and experimental research articles, short clinical reports, review articles and letters to the editor are welcome on topics such as : • Dysmorphology and syndrome delineation • Molecular genetics and molecular cytogenetics of inherited disorders • Clinical applications of genomics and nextgen sequencing technologies • Syndromal cancer genetics • Behavioral genetics • Community genetics • Fetal pathology and prenatal diagnosis • Genetic counseling.
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