KEGG   DISEASE: 感染誘発性急性脳症
エントリ  
H02536                                                             
名称    
感染誘発性急性脳症
  下位グループ
単純ヘルペス脳炎 (HSE)
急性壊死性脳症 (ADANE)
概要    
Infection-induced acute encephalopathy (IIAE) is a severe neurologic complication of an infection that usually occurs in children. It is characterized by a high-grade fever, often leading to coma, multiple-organ failure, brain edema, and high morbidity and mortality. The infections are usually viral, such as influenza, parainfluenza, and herpes simplex virus. It is possible that genetic factors play an important role in the aetiology of IIAE. For example, herpes simplex encephalitis (HSE) has been linked to defects in type I interferon production downstream of Toll-like receptor (TLR)3.
カテゴリ  
神経系疾患; 感染症
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 01 感染症・寄生虫症
  中枢神経系のウイルス感染症
   1C80  ウイルス性脳炎, 他に分類されないもの
    H02536  感染誘発性急性脳症
パスウェイに基づく疾患分類 [BR:jp08402]
 細胞プロセス
  nt06527  ネクロトーシス
   H02536  感染誘発性急性脳症
 免疫系
  nt06517  TLR シグナリング
   H02536  感染誘発性急性脳症
  nt06519  RLR シグナリング
   H02536  感染誘発性急性脳症
パスウェイ 
hsa04620  Toll-like receptor signaling pathway
hsa04621  NOD-like receptor signaling pathway
hsa05164  Influenza A
hsa05168  Herpes simplex virus 1 infection
hsa04217  Necroptosis
ネットワーク
nt06517 TLR signaling
nt06519 RLR signaling
nt06527 Necroptosis
病因遺伝子 
(IIAE1) UNC93B1 [HSA:81622] [KO:K26150]
(IIAE2) TLR3 [HSA:7098] [KO:K05401]
(IIAE3) RANBP2 [HSA:5903] [KO:K12172]
(IIAE4) CPT2 [HSA:1376] [KO:K08766]
(IIAE5) TRAF3 [HSA:7187] [KO:K03174]
(IIAE6) TICAM1 [HSA:148022] [KO:K05842]
(IIAE7) IRF3 [HSA:3661] [KO:K05411]
(IIAE8) TBK1 [HSA:29110] [KO:K05410]
(IIAE9) NUP214 [HSA:8021] [KO:K14317]
(IIAE10) SNORA31 [HSA:677814] [KO:K26336]
(IIAE11) DBR1 [HSA:51163] [KO:K18328]
(IIAE12) RNH1 [HSA:6050] [KO:K16634]
病原体   
Human herpesvirus 1 [GN:T40073]
Human herpesvirus 2 [GN:T40074]
Influenza A virus [GN:T40035 T40036 T40037 T40038]
influenza B virus [GN:T40039]
Human parainfluenza virus 2 [GN:T40042]
リンク   
ICD-11: 1C80
MeSH: D000069544
OMIM: 610551 613002 608033 614212 614849 614850 616532 617900 618426 619396 619441 620461
文献    
  著者
Casrouge A, Zhang SY, Eidenschenk C, Jouanguy E, Puel A, Yang K, Alcais A, Picard C, Mahfoufi N, Nicolas N, Lorenzo L, Plancoulaine S, Senechal B, Geissmann F, Tabeta K, Hoebe K, Du X, Miller RL, Heron B, Mignot C, de Villemeur TB, Lebon P, Dulac O, Rozenberg F, Beutler B, Tardieu M, Abel L, Casanova JL
  タイトル
Herpes simplex virus encephalitis in human UNC-93B deficiency.
  雑誌
Science 314:308-12 (2006)
DOI:10.1126/science.1128346
文献    
  著者
Lafaille FG, Pessach IM, Zhang SY, Ciancanelli MJ, Herman M, Abhyankar A, Ying SW, Keros S, Goldstein PA, Mostoslavsky G, Ordovas-Montanes J, Jouanguy E, Plancoulaine S, Tu E, Elkabetz Y, Al-Muhsen S, Tardieu M, Schlaeger TM, Daley GQ, Abel L, Casanova JL, Studer L, Notarangelo LD
  タイトル
Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells.
  雑誌
Nature 491:769-73 (2012)
DOI:10.1038/nature11583
文献    
  著者
Neilson DE, Adams MD, Orr CM, Schelling DK, Eiben RM, Kerr DS, Anderson J, Bassuk AG, Bye AM, Childs AM, Clarke A, Crow YJ, Di Rocco M, Dohna-Schwake C, Dueckers G, Fasano AE, Gika AD, Gionnis D, Gorman MP, Grattan-Smith PJ, Hackenberg A, Kuster A, Lentschig MG, Lopez-Laso E, Marco EJ, Mastroyianni S, Perrier J, Schmitt-Mechelke T, Servidei S, Skardoutsou A, Uldall P, van der Knaap MS, Goglin KC, Tefft DL, Aubin C, de Jager P, Hafler D, Warman ML
  タイトル
Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.
  雑誌
Am J Hum Genet 84:44-51 (2009)
DOI:10.1016/j.ajhg.2008.12.009
文献    
  著者
Chen Y, Mizuguchi H, Yao D, Ide M, Kuroda Y, Shigematsu Y, Yamaguchi S, Yamaguchi M, Kinoshita M, Kido H
  タイトル
Thermolabile phenotype of carnitine palmitoyltransferase II variations as a predisposing factor for influenza-associated encephalopathy.
  雑誌
FEBS Lett 579:2040-4 (2005)
DOI:10.1016/j.febslet.2005.02.050
文献    
  著者
Mork N, Kofod-Olsen E, Sorensen KB, Bach E, Orntoft TF, Ostergaard L, Paludan SR, Christiansen M, Mogensen TH
  タイトル
Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis.
  雑誌
Genes Immun 16:552-66 (2015)
DOI:10.1038/gene.2015.46
文献    
PMID:31178128 (IIAE9)
  著者
Fichtman B, Harel T, Biran N, Zagairy F, Applegate CD, Salzberg Y, Gilboa T, Salah S, Shaag A, Simanovsky N, Ayoubieh H, Sobreira N, Punzi G, Pierri CL, Hamosh A, Elpeleg O, Harel A, Edvardson S
  タイトル
Pathogenic Variants in NUP214 Cause "Plugged" Nuclear Pore Channels and Acute Febrile Encephalopathy.
  雑誌
Am J Hum Genet 105:48-64 (2019)
DOI:10.1016/j.ajhg.2019.05.003
文献    
PMID:31806906 (IIAE10)
  著者
Lafaille FG, Harschnitz O, Lee YS, Zhang P, Hasek ML, Kerner G, Itan Y, Ewaleifoh O, Rapaport F, Carlile TM, Carter-Timofte ME, Paquet D, Dobbs K, Zimmer B, Gao D, Rojas-Duran MF, Kwart D, Rattina V, Ciancanelli MJ, McAlpine JL, Lorenzo L, Boucherit S, Rozenberg F, Halwani R, Henry B, Amenzoui N, Alsum Z, Marques L, Church JA, Al-Muhsen S, Tardieu M, Bousfiha AA, Paludan SR, Mogensen TH, Quintana-Murci L, Tessier-Lavigne M, Smith GA, Notarangelo LD, Studer L, Gilbert W, Abel L, Casanova JL, Zhang SY
  タイトル
Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis.
  雑誌
Nat Med 25:1873-1884 (2019)
DOI:10.1038/s41591-019-0672-3
文献    
PMID:29474921 (IIAE11)
  著者
Zhang SY, Clark NE, Freije CA, Pauwels E, Taggart AJ, Okada S, Mandel H, Garcia P, Ciancanelli MJ, Biran A, Lafaille FG, Tsumura M, Cobat A, Luo J, Volpi S, Zimmer B, Sakata S, Dinis A, Ohara O, Garcia Reino EJ, Dobbs K, Hasek M, Holloway SP, McCammon K, Hussong SA, DeRosa N, Van Skike CE, Katolik A, Lorenzo L, Hyodo M, Faria E, Halwani R, Fukuhara R, Smith GA, Galvan V, Damha MJ, Al-Muhsen S, Itan Y, Boeke JD, Notarangelo LD, Studer L, Kobayashi M, Diogo L, Fairbrother WG, Abel L, Rosenberg BR, Hart PJ, Etzioni A, Casanova JL
  タイトル
Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection.
  雑誌
Cell 172:952-965.e18 (2018)
DOI:10.1016/j.cell.2018.02.019
文献    
PMID:36935417 (IIAE12)
  著者
Hedberg-Oldfors C, Mitra S, Molinaro A, Visuttijai K, Fogelstrand L, Oldfors A, Sterky FH, Darin N
  タイトル
Ribonuclease inhibitor 1 (RNH1) deficiency cause congenital cataracts and global developmental delay with infection-induced psychomotor regression and anemia.
  雑誌
Eur J Hum Genet 31:887-894 (2023)
DOI:10.1038/s41431-023-01327-7
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