메뉴 건너뛰기




Volumn 37, Issue 2, 2017, Pages 123-132

Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease

Author keywords

autoinflammation; autoinflammatory disease; Interferon; interferonopathy

Indexed keywords

INTERFERON; TYPE 1 INTERFERON; UNCLASSIFIED DRUG; BIOLOGICAL MARKER; INTERFERON REGULATORY FACTOR;

EID: 85003819946     PISSN: 02719142     EISSN: 15732592     Source Type: Journal    
DOI: 10.1007/s10875-016-0359-1     Document Type: Article
Times cited : (145)

References (45)
  • 1
    • 82555192885 scopus 로고    scopus 로고
    • Type I, interferonopathies: a novel set of inborn errors of immunity
    • COI: 1:CAS:528:DC%2BC38Xhsl2jtbs%3D, PID: 22129056
    • Crow YJ. Type I, interferonopathies: a novel set of inborn errors of immunity. Ann N Y Acad Sci. 2011;1238:91–8.
    • (2011) Ann N Y Acad Sci , vol.1238 , pp. 91-98
    • Crow, Y.J.1
  • 2
    • 84933279572 scopus 로고    scopus 로고
    • Aicardi-Goutieres syndrome and the type I interferonopathies
    • COI: 1:CAS:528:DC%2BC2MXhtFeju7zJ, PID: 26052098
    • Crow YJ, Manel N. Aicardi-Goutieres syndrome and the type I interferonopathies. Nat Rev Immunol. 2015;15(7):429–40.
    • (2015) Nat Rev Immunol , vol.15 , Issue.7 , pp. 429-440
    • Crow, Y.J.1    Manel, N.2
  • 3
    • 84971578594 scopus 로고    scopus 로고
    • Personalized immunomonitoring uncovers molecular networks that stratify lupus patients
    • COI: 1:CAS:528:DC%2BC28Xpslalt70%3D, PID: 27259156
    • Banchereau R, Hong S, Cantarel B, et al. Personalized immunomonitoring uncovers molecular networks that stratify lupus patients. Cell. 2016;165(6):1548–50.
    • (2016) Cell , vol.165 , Issue.6 , pp. 1548-1550
    • Banchereau, R.1    Hong, S.2    Cantarel, B.3
  • 4
    • 20944450759 scopus 로고    scopus 로고
    • Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis
    • COI: 1:CAS:528:DC%2BD2MXkvFykt78%3D, PID: 15852401
    • Greenberg SA, Pinkus JL, Pinkus GS, et al. Interferon-alpha/beta-mediated innate immune mechanisms in dermatomyositis. Ann Neurol. 2005;57(5):664–78.
    • (2005) Ann Neurol , vol.57 , Issue.5 , pp. 664-678
    • Greenberg, S.A.1    Pinkus, J.L.2    Pinkus, G.S.3
  • 5
    • 85001022736 scopus 로고    scopus 로고
    • Efficacy of the Janus Kinase 1/2 Inhibitor Ruxolitinib in the Treatment of Vasculopathy Associated with TMEM173-Activating Mutations in three children
    • Frémond ML, Rodero MP, Jeremiah N, et al. Efficacy of the Janus Kinase 1/2 Inhibitor Ruxolitinib in the Treatment of Vasculopathy Associated with TMEM173-Activating Mutations in three children. J Allergy Clin Immunol. 2016.
    • (2016) J Allergy Clin Immunol
    • Frémond, M.L.1    Rodero, M.P.2    Jeremiah, N.3
  • 6
    • 0031593632 scopus 로고    scopus 로고
    • Aicardi-Goutieres syndrome: an update and results of interferon-alpha studies
    • COI: 1:STN:280:DyaK1M%2Fms1Omuw%3D%3D, PID: 9851434
    • Goutieres F, Aicardi J, Barth PG, Lebon P. Aicardi-Goutieres syndrome: an update and results of interferon-alpha studies. Ann Neurol. 1998;44(6):900–7.
    • (1998) Ann Neurol , vol.44 , Issue.6 , pp. 900-907
    • Goutieres, F.1    Aicardi, J.2    Barth, P.G.3    Lebon, P.4
  • 7
    • 4244215954 scopus 로고    scopus 로고
    • Interferon and Aicardi-Goutieres syndrome
    • PID: 12365361, discussion A55-48, A77-86
    • Lebon P, Meritet JF, Krivine A, Rozenberg F. Interferon and Aicardi-Goutieres syndrome. Eur J Paediatr Neurol. 2002;6(Suppl A):A47–53. discussion A55-48, A77-86.
    • (2002) Eur J Paediatr Neurol , vol.6 , pp. A47-A53
    • Lebon, P.1    Meritet, J.F.2    Krivine, A.3    Rozenberg, F.4
  • 8
    • 33745034931 scopus 로고    scopus 로고
    • Functional assay of type I interferon in systemic lupus erythematosus plasma and association with anti-RNA binding protein autoantibodies
    • COI: 1:CAS:528:DC%2BD28Xms1Sisr8%3D, PID: 16736505
    • Hua J, Kirou K, Lee C, Crow MK. Functional assay of type I interferon in systemic lupus erythematosus plasma and association with anti-RNA binding protein autoantibodies. Arthritis Rheum. 2006;54(6):1906–16.
    • (2006) Arthritis Rheum , vol.54 , Issue.6 , pp. 1906-1916
    • Hua, J.1    Kirou, K.2    Lee, C.3    Crow, M.K.4
  • 9
    • 66449121844 scopus 로고    scopus 로고
    • Elevated serum interferon-alpha activity in juvenile dermatomyositis: associations with disease activity at diagnosis and after thirty-six months of therapy
    • COI: 1:CAS:528:DC%2BD1MXotVeqt70%3D, PID: 19479879
    • Niewold TB, Kariuki SN, Morgan GA, Shrestha S, Pachman LM. Elevated serum interferon-alpha activity in juvenile dermatomyositis: associations with disease activity at diagnosis and after thirty-six months of therapy. Arthritis Rheum. 2009;60(6):1815–24.
    • (2009) Arthritis Rheum , vol.60 , Issue.6 , pp. 1815-1824
    • Niewold, T.B.1    Kariuki, S.N.2    Morgan, G.A.3    Shrestha, S.4    Pachman, L.M.5
  • 10
    • 68549096262 scopus 로고    scopus 로고
    • Validation of a HeLa Mx2/Luc reporter cell line for the quantification of human type I interferons
    • COI: 1:CAS:528:DC%2BD1MXhtFOhtrbK, PID: 19684437
    • Seo YJ, Kim GH, Kwak HJ, et al. Validation of a HeLa Mx2/Luc reporter cell line for the quantification of human type I interferons. Pharmacology. 2009;84(3):135–44.
    • (2009) Pharmacology , vol.84 , Issue.3 , pp. 135-144
    • Seo, Y.J.1    Kim, G.H.2    Kwak, H.J.3
  • 11
    • 77952279398 scopus 로고    scopus 로고
    • Monocyte surface expression of Fcgamma receptor RI (CD64), a biomarker reflecting type-I interferon levels in systemic lupus erythematosus
    • PID: 20478071
    • Li Y, Lee PY, Kellner ES, et al. Monocyte surface expression of Fcgamma receptor RI (CD64), a biomarker reflecting type-I interferon levels in systemic lupus erythematosus. Arthritis Res Ther. 2010;12(3):R90.
    • (2010) Arthritis Res Ther , vol.12 , Issue.3 , pp. R90
    • Li, Y.1    Lee, P.Y.2    Kellner, E.S.3
  • 12
    • 80053593989 scopus 로고    scopus 로고
    • A vesicular stomatitis virus replicon-based bioassay for the rapid and sensitive determination of multi-species type I interferon
    • PID: 21998709
    • Berger Rentsch M, Zimmer G. A vesicular stomatitis virus replicon-based bioassay for the rapid and sensitive determination of multi-species type I interferon. PLoS One. 2011;6(10), e25858.
    • (2011) PLoS One , vol.6 , Issue.10
    • Berger Rentsch, M.1    Zimmer, G.2
  • 13
    • 0037451167 scopus 로고    scopus 로고
    • Interferon and granulopoiesis signatures in systemic lupus erythematosus blood
    • COI: 1:CAS:528:DC%2BD3sXitlOgs74%3D, PID: 12642603
    • Bennett L, Palucka AK, Arce E, et al. Interferon and granulopoiesis signatures in systemic lupus erythematosus blood. J Exp Med. 2003;197(6):711–23.
    • (2003) J Exp Med , vol.197 , Issue.6 , pp. 711-723
    • Bennett, L.1    Palucka, A.K.2    Arce, E.3
  • 14
    • 0344492212 scopus 로고    scopus 로고
    • Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus
    • COI: 1:CAS:528:DC%2BD3sXitVaisb8%3D, PID: 12604793
    • Baechler EC, Batliwalla FM, Karypis G, et al. Interferon-inducible gene expression signature in peripheral blood cells of patients with severe lupus. Proc Natl Acad Sci U S A. 2003;100(5):2610–5.
    • (2003) Proc Natl Acad Sci U S A , vol.100 , Issue.5 , pp. 2610-2615
    • Baechler, E.C.1    Batliwalla, F.M.2    Karypis, G.3
  • 15
    • 84887607415 scopus 로고    scopus 로고
    • Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case–control study
    • COI: 1:CAS:528:DC%2BC3sXhslWlsb3L, PID: 24183309
    • Rice GI, Forte GM, Szynkiewicz M, et al. Assessment of interferon-related biomarkers in Aicardi-Goutieres syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case–control study. Lancet Neurol. 2013;12(12):1159–69.
    • (2013) Lancet Neurol , vol.12 , Issue.12 , pp. 1159-1169
    • Rice, G.I.1    Forte, G.M.2    Szynkiewicz, M.3
  • 16
    • 84868207785 scopus 로고    scopus 로고
    • Mutations in ADAR1 cause Aicardi-Goutieres syndrome associated with a type I interferon signature
    • COI: 1:CAS:528:DC%2BC38Xhtlymur3E, PID: 23001123
    • Rice GI, Kasher PR, Forte GM, et al. Mutations in ADAR1 cause Aicardi-Goutieres syndrome associated with a type I interferon signature. Nat Genet. 2012;44(11):1243–8.
    • (2012) Nat Genet , vol.44 , Issue.11 , pp. 1243-1248
    • Rice, G.I.1    Kasher, P.R.2    Forte, G.M.3
  • 17
    • 34248998426 scopus 로고    scopus 로고
    • An interferon signature in the peripheral blood of dermatomyositis patients is associated with disease activity
    • COI: 1:CAS:528:DC%2BD2sXmt12rsLg%3D, PID: 17515957
    • Baechler EC, Bauer JW, Slattery CA, et al. An interferon signature in the peripheral blood of dermatomyositis patients is associated with disease activity. Mol Med. 2007;13(1–2):59–68.
    • (2007) Mol Med , vol.13 , Issue.1-2 , pp. 59-68
    • Baechler, E.C.1    Bauer, J.W.2    Slattery, C.A.3
  • 18
    • 84899495767 scopus 로고    scopus 로고
    • Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling
    • COI: 1:CAS:528:DC%2BC2cXltFKqsrY%3D, PID: 24686847
    • Rice GI, Del Toro DY, Jenkinson EM, et al. Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling. Nat Genet. 2014;46(5):503–9.
    • (2014) Nat Genet , vol.46 , Issue.5 , pp. 503-509
    • Rice, G.I.1    Del Toro, D.Y.2    Jenkinson, E.M.3
  • 19
    • 84894063757 scopus 로고    scopus 로고
    • A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1
    • COI: 1:CAS:528:DC%2BC2cXlt1Sht74%3D, PID: 24262145
    • Livingston JH, Lin JP, Dale RC, et al. A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1. J Med Genet. 2014;51(2):76–82.
    • (2014) J Med Genet , vol.51 , Issue.2 , pp. 76-82
    • Livingston, J.H.1    Lin, J.P.2    Dale, R.C.3
  • 20
    • 33746581694 scopus 로고    scopus 로고
    • Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutieres syndrome at the AGS1 locus
    • COI: 1:CAS:528:DC%2BD28XnsVCgsro%3D, PID: 16845398
    • Crow YJ, Hayward BE, Parmar R, et al. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutieres syndrome at the AGS1 locus. Nat Genet. 2006;38(8):917–20.
    • (2006) Nat Genet , vol.38 , Issue.8 , pp. 917-920
    • Crow, Y.J.1    Hayward, B.E.2    Parmar, R.3
  • 21
    • 33746522835 scopus 로고    scopus 로고
    • Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection
    • COI: 1:CAS:528:DC%2BD28XnsVCgsrw%3D, PID: 16845400
    • Crow YJ, Leitch A, Hayward BE, et al. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutieres syndrome and mimic congenital viral brain infection. Nat Genet. 2006;38(8):910–6.
    • (2006) Nat Genet , vol.38 , Issue.8 , pp. 910-916
    • Crow, Y.J.1    Leitch, A.2    Hayward, B.E.3
  • 22
    • 67649861901 scopus 로고    scopus 로고
    • Mutations involved in Aicardi-Goutieres syndrome implicate SAMHD1 as regulator of the innate immune response
    • COI: 1:CAS:528:DC%2BD1MXnt1Shtr0%3D, PID: 19525956
    • Rice GI, Bond J, Asipu A, et al. Mutations involved in Aicardi-Goutieres syndrome implicate SAMHD1 as regulator of the innate immune response. Nat Genet. 2009;41(7):829–32.
    • (2009) Nat Genet , vol.41 , Issue.7 , pp. 829-832
    • Rice, G.I.1    Bond, J.2    Asipu, A.3
  • 23
    • 79251551861 scopus 로고    scopus 로고
    • Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature
    • COI: 1:CAS:528:DC%2BC3MXjtVOjsg%3D%3D, PID: 21217755
    • Briggs TA, Rice GI, Daly S, et al. Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature. Nat Genet. 2011;43(2):127–31.
    • (2011) Nat Genet , vol.43 , Issue.2 , pp. 127-131
    • Briggs, T.A.1    Rice, G.I.2    Daly, S.3
  • 24
    • 79251564299 scopus 로고    scopus 로고
    • Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity
    • COI: 1:CAS:528:DC%2BC3MXjtVOiug%3D%3D, PID: 21217752
    • Lausch E, Janecke A, Bros M, et al. Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity. Nat Genet. 2011;43(2):132–7.
    • (2011) Nat Genet , vol.43 , Issue.2 , pp. 132-137
    • Lausch, E.1    Janecke, A.2    Bros, M.3
  • 25
    • 84905825645 scopus 로고    scopus 로고
    • Activated STING in a vascular and pulmonary syndrome
    • PID: 25029335
    • Liu Y, Jesus AA, Marrero B, et al. Activated STING in a vascular and pulmonary syndrome. N Engl J Med. 2014;371(6):507–18.
    • (2014) N Engl J Med , vol.371 , Issue.6 , pp. 507-518
    • Liu, Y.1    Jesus, A.A.2    Marrero, B.3
  • 26
    • 78049496573 scopus 로고    scopus 로고
    • C1q deficiency leads to the defective suppression of IFN-alpha in response to nucleoprotein containing immune complexes
    • COI: 1:CAS:528:DC%2BC3cXht1Ggu7nE, PID: 20844193
    • Santer DM, Hall BE, George TC, et al. C1q deficiency leads to the defective suppression of IFN-alpha in response to nucleoprotein containing immune complexes. J Immunol. 2010;185(8):4738–49.
    • (2010) J Immunol , vol.185 , Issue.8 , pp. 4738-4749
    • Santer, D.M.1    Hall, B.E.2    George, T.C.3
  • 27
    • 84922880395 scopus 로고    scopus 로고
    • Human intracellular ISG15 prevents interferon-alpha/beta over-amplification and auto-inflammation
    • COI: 1:CAS:528:DC%2BC2cXhvVemtrjP, PID: 25307056
    • Zhang X, Bogunovic D, Payelle-Brogard B, et al. Human intracellular ISG15 prevents interferon-alpha/beta over-amplification and auto-inflammation. Nature. 2015;517(7532):89–93.
    • (2015) Nature , vol.517 , Issue.7532 , pp. 89-93
    • Zhang, X.1    Bogunovic, D.2    Payelle-Brogard, B.3
  • 28
    • 84906230645 scopus 로고    scopus 로고
    • The SKIV2L RNA exosome limits activation of the RIG-I-like receptors
    • COI: 1:CAS:528:DC%2BC2cXht1ait7%2FK, PID: 25064072
    • Eckard SC, Rice GI, Fabre A, et al. The SKIV2L RNA exosome limits activation of the RIG-I-like receptors. Nat Immunol. 2014;15(9):839–45.
    • (2014) Nat Immunol , vol.15 , Issue.9 , pp. 839-845
    • Eckard, S.C.1    Rice, G.I.2    Fabre, A.3
  • 29
    • 84946780874 scopus 로고    scopus 로고
    • Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production
    • PID: 26524591
    • Brehm A, Liu Y, Sheikh A, et al. Additive loss-of-function proteasome subunit mutations in CANDLE/PRAAS patients promote type I IFN production. J Clin Invest. 2015;125(11):4196–211.
    • (2015) J Clin Invest , vol.125 , Issue.11 , pp. 4196-4211
    • Brehm, A.1    Liu, Y.2    Sheikh, A.3
  • 30
    • 84925137606 scopus 로고    scopus 로고
    • Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome
    • COI: 1:CAS:528:DC%2BC2MXhsVakur0%3D, PID: 25620203
    • Jang MA, Kim EK, Now H, et al. Mutations in DDX58, which encodes RIG-I, cause atypical Singleton-Merten syndrome. Am J Hum Genet. 2015;96(2):266–74.
    • (2015) Am J Hum Genet , vol.96 , Issue.2 , pp. 266-274
    • Jang, M.A.1    Kim, E.K.2    Now, H.3
  • 31
    • 84961696302 scopus 로고    scopus 로고
    • DNA polymerase-alpha regulates the activation of type I interferons through cytosolic RNA:DNA synthesis
    • COI: 1:CAS:528:DC%2BC28XkvV2jtLs%3D, PID: 27019227
    • Starokadomskyy P, Gemelli T, Rios JJ, et al. DNA polymerase-alpha regulates the activation of type I interferons through cytosolic RNA:DNA synthesis. Nat Immunol. 2016;17(5):495–504.
    • (2016) Nat Immunol , vol.17 , Issue.5 , pp. 495-504
    • Starokadomskyy, P.1    Gemelli, T.2    Rios, J.J.3
  • 32
    • 84977640575 scopus 로고    scopus 로고
    • Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
    • PID: 27325888
    • Meuwissen ME, Schot R, Buta S, et al. Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome. J Exp Med. 2016;213(7):1163–74.
    • (2016) J Exp Med , vol.213 , Issue.7 , pp. 1163-1174
    • Meuwissen, M.E.1    Schot, R.2    Buta, S.3
  • 33
    • 84999850013 scopus 로고    scopus 로고
    • Type I interferon-mediated monogenic autoinflammation: the type I interferonopathies, a conceptual overview
    • COI: 1:CAS:528:DC%2BC2sXitlWiu7Y%3D, PID: 27821552
    • Rodero MP, Crow YJ. Type I interferon-mediated monogenic autoinflammation: the type I interferonopathies, a conceptual overview. J Exp Med. 2016;213(12):2527–38.
    • (2016) J Exp Med , vol.213 , Issue.12 , pp. 2527-2538
    • Rodero, M.P.1    Crow, Y.J.2
  • 34
    • 84895461649 scopus 로고    scopus 로고
    • Early-onset stroke and vasculopathy associated with mutations in ADA2
    • COI: 1:CAS:528:DC%2BC2cXkt1ehsLY%3D, PID: 24552284
    • Zhou Q, Yang D, Ombrello AK, et al. Early-onset stroke and vasculopathy associated with mutations in ADA2. N Engl J Med. 2014;370(10):911–20.
    • (2014) N Engl J Med , vol.370 , Issue.10 , pp. 911-920
    • Zhou, Q.1    Yang, D.2    Ombrello, A.K.3
  • 35
    • 84895465707 scopus 로고    scopus 로고
    • Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy
    • PID: 24552285
    • Navon Elkan P, Pierce SB, Segel R, et al. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. N Engl J Med. 2014;370(10):921–31.
    • (2014) N Engl J Med , vol.370 , Issue.10 , pp. 921-931
    • Navon Elkan, P.1    Pierce, S.B.2    Segel, R.3
  • 36
    • 67649881103 scopus 로고    scopus 로고
    • RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection
    • COI: 1:CAS:528:DC%2BD1MXnt1ShsLw%3D, PID: 19525954
    • Henneke M, Diekmann S, Ohlenbusch A, et al. RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection. Nat Genet. 2009;41(7):773–5.
    • (2009) Nat Genet , vol.41 , Issue.7 , pp. 773-775
    • Henneke, M.1    Diekmann, S.2    Ohlenbusch, A.3
  • 37
    • 84963648036 scopus 로고    scopus 로고
    • Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutieres syndrome
    • PID: 27091087
    • Tonduti D, Orcesi S, Jenkinson EM, et al. Clinical, radiological and possible pathological overlap of cystic leukoencephalopathy without megalencephaly and Aicardi-Goutieres syndrome. Eur J Paediatr Neurol. 2016;20(4):604–10.
    • (2016) Eur J Paediatr Neurol , vol.20 , Issue.4 , pp. 604-610
    • Tonduti, D.1    Orcesi, S.2    Jenkinson, E.M.3
  • 38
    • 84942619984 scopus 로고    scopus 로고
    • PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity
    • COI: 1:CAS:528:DC%2BC2MXlvVSqt7s%3D, PID: 25842288, e1575
    • Mathieu AL, Verronese E, Rice GI, et al. PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity. J Allergy Clin Immunol. 2015;135(6):1578–88. e1575.
    • (2015) J Allergy Clin Immunol , vol.135 , Issue.6 , pp. 1578-1588
    • Mathieu, A.L.1    Verronese, E.2    Rice, G.I.3
  • 39
    • 84908584244 scopus 로고    scopus 로고
    • Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)
    • COI: 1:CAS:528:DC%2BC2cXhvFWqsL%2FE, PID: 25193871
    • Chakraborty PK, Schmitz-Abe K, Kennedy EK, et al. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD). Blood. 2014;124(18):2867–71.
    • (2014) Blood , vol.124 , Issue.18 , pp. 2867-2871
    • Chakraborty, P.K.1    Schmitz-Abe, K.2    Kennedy, E.K.3
  • 40
    • 82255192363 scopus 로고    scopus 로고
    • Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus
    • COI: 1:CAS:528:DC%2BC3MXhtlGksL%2FF, PID: 22019780
    • Al-Mayouf SM, Sunker A, Abdwani R, et al. Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus. Nat Genet. 2011;43(12):1186–8.
    • (2011) Nat Genet , vol.43 , Issue.12 , pp. 1186-1188
    • Al-Mayouf, S.M.1    Sunker, A.2    Abdwani, R.3
  • 41
    • 84976583862 scopus 로고    scopus 로고
    • Digestion of chromatin in apoptotic cell microparticles prevents autoimmunity
    • COI: 1:CAS:528:DC%2BC28XpslWlt74%3D, PID: 27293190
    • Sisirak V, Sally B, D’Agati V, et al. Digestion of chromatin in apoptotic cell microparticles prevents autoimmunity. Cell. 2016;166(1):88–101.
    • (2016) Cell , vol.166 , Issue.1 , pp. 88-101
    • Sisirak, V.1    Sally, B.2    D’Agati, V.3
  • 42
    • 34548436508 scopus 로고    scopus 로고
    • Blood leukocyte microarrays to diagnose systemic onset juvenile idiopathic arthritis and follow the response to IL-1 blockade
    • COI: 1:CAS:528:DC%2BD2sXhtVWnurnM, PID: 17724127
    • Allantaz F, Chaussabel D, Stichweh D, et al. Blood leukocyte microarrays to diagnose systemic onset juvenile idiopathic arthritis and follow the response to IL-1 blockade. J Exp Med. 2007;204(9):2131–44.
    • (2007) J Exp Med , vol.204 , Issue.9 , pp. 2131-2144
    • Allantaz, F.1    Chaussabel, D.2    Stichweh, D.3
  • 43
    • 79953323633 scopus 로고    scopus 로고
    • A multicentre, randomised, double-blind, placebo-controlled trial with the interleukin-1 receptor antagonist anakinra in patients with systemic-onset juvenile idiopathic arthritis (ANAJIS trial)
    • COI: 1:CAS:528:DC%2BC3MXnt1egsLc%3D, PID: 21173013
    • Quartier P, Allantaz F, Cimaz R, et al. A multicentre, randomised, double-blind, placebo-controlled trial with the interleukin-1 receptor antagonist anakinra in patients with systemic-onset juvenile idiopathic arthritis (ANAJIS trial). Ann Rheum Dis. 2011;70(5):747–54.
    • (2011) Ann Rheum Dis , vol.70 , Issue.5 , pp. 747-754
    • Quartier, P.1    Allantaz, F.2    Cimaz, R.3
  • 44
    • 85013856678 scopus 로고    scopus 로고
    • Paradoxical psoriasis—unabated type I IFN production induced by TNF blockade
    • Conrad CD, Domizio JD, Mylonas A, et al. Paradoxical psoriasis—unabated type I IFN production induced by TNF blockade. Cytokine. 2015;76:66–112.
    • (2015) Cytokine , vol.76 , pp. 66-112
    • Conrad, C.D.1    Domizio, J.D.2    Mylonas, A.3
  • 45
    • 85048742182 scopus 로고    scopus 로고
    • Targeted therapeutics in SLE: emerging strategies to modulate the interferon pathway
    • Oon S, Wilson NJ, Wicks I. Targeted therapeutics in SLE: emerging strategies to modulate the interferon pathway. Clin Transl Immunol. 2016;5(5), e79.
    • (2016) Clin Transl Immunol , vol.5 , Issue.5
    • Oon, S.1    Wilson, N.J.2    Wicks, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.