Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/48631
Campo DC Valoridioma
dc.contributor.authorPicard, Capucineen_US
dc.contributor.authorVon Bernuth, Horsten_US
dc.contributor.authorGhandil, Pegahen_US
dc.contributor.authorChrabieh, Mayaen_US
dc.contributor.authorLevy, Oferen_US
dc.contributor.authorArkwright, Peter D.en_US
dc.contributor.authorMcDonald, Douglasen_US
dc.contributor.authorGeha, Raif S.en_US
dc.contributor.authorTakada, Hidetoshien_US
dc.contributor.authorKrause, Jens C.en_US
dc.contributor.authorCreech, C. Buddyen_US
dc.contributor.authorKu, Cheng Lungen_US
dc.contributor.authorEhl, Stephanen_US
dc.contributor.authorMaródi, Lászlóen_US
dc.contributor.authorAl-Muhsen, Salehen_US
dc.contributor.authorAl-Hajjar, Samien_US
dc.contributor.authorAl-Ghonaium, Abdulazizen_US
dc.contributor.authorDay-Good, Noorbibi K.en_US
dc.contributor.authorHolland, Steven M.en_US
dc.contributor.authorGallin, John I.en_US
dc.contributor.authorChapel, Helenen_US
dc.contributor.authorSpeert, David P.en_US
dc.contributor.authorRodriguez-Gallego, Carlosen_US
dc.contributor.authorColino, Elenaen_US
dc.contributor.authorGarty, Ben Zionen_US
dc.contributor.authorRoifman, Chaimen_US
dc.contributor.authorHara, Toshiroen_US
dc.contributor.authorYoshikawa, Hidetoen_US
dc.contributor.authorNonoyama, Shigeakien_US
dc.contributor.authorDomachowske, Josephen_US
dc.contributor.authorIssekutz, Andrew C.en_US
dc.contributor.authorTang, Mimien_US
dc.contributor.authorSmart, Joanneen_US
dc.contributor.authorZitnik, Simona Evaen_US
dc.contributor.authorHoarau, Cyrilleen_US
dc.contributor.authorKumararatne, Dinakantha S.en_US
dc.contributor.authorThrasher, Adrian J.en_US
dc.contributor.authorDavies, E. Grahamen_US
dc.contributor.authorBethune, Claireen_US
dc.contributor.authorSirvent, Nicolasen_US
dc.contributor.authorDe Ricaud, Dominiqueen_US
dc.contributor.authorCamcioglu, Yildizen_US
dc.contributor.authorVasconcelos, Júliaen_US
dc.contributor.authorGuedes, Margaridaen_US
dc.contributor.authorVitor, Artur Bonitoen_US
dc.contributor.authorRodrigo, Carlosen_US
dc.contributor.authorAlmazán, Franciscoen_US
dc.contributor.authorMéndez, Mariaen_US
dc.contributor.authorAróstegui, Juan Ignacioen_US
dc.contributor.authorAlsina, Laiaen_US
dc.contributor.authorFortuny, Claudiaen_US
dc.contributor.authorReichenbach, Janineen_US
dc.contributor.authorVerbsky, James W.en_US
dc.contributor.authorBossuyt, Xavieren_US
dc.contributor.authorDoffinger, Raineren_US
dc.contributor.authorAbel, Laurenten_US
dc.contributor.authorPuel, Anneen_US
dc.contributor.authorCasanova, Jean Laurenten_US
dc.date.accessioned2018-11-23T23:33:57Z-
dc.date.available2018-11-23T23:33:57Z-
dc.date.issued2010en_US
dc.identifier.issn0025-7974en_US
dc.identifier.urihttp://hdl.handle.net/10553/48631-
dc.description.abstractAutosomal recessive interleukin-1 receptor-associated kinase (IRAK)-4 and myeloid differentiation factor (MyD)88 deficiencies impair Toll-like receptor (TLR)- and interleukin-1 receptor-mediated immunity. We documented the clinical features and outcome of 48 patients with IRAK-4 deficiency and 12 patients with MyD88 deficiency, from 37 kindreds in 15 countries.The clinical features of IRAK-4 and MyD88 deficiency were indistinguishable. There were no severe viral, parasitic, and fungal diseases, and the range of bacterial infections was narrow. Noninvasive bacterial infections occurred in 52 patients, with a high incidence of infections of the upper respiratory tract and the skin, mostly caused by Pseudomonas aeruginosa and Staphylococcus aureus, respectively. The leading threat was invasive pneumococcal disease, documented in 41 patients (68%) and causing 72 documented invasive infections (52.2%). P. aeruginosa and Staph. aureus documented invasive infections also occurred (16.7% and 16%, respectively, in 13 and 13 patients, respectively). Systemic signs of inflammation were usually weak or delayed. The first invasive infection occurred before the age of 2 years in 53 (88.3%) and in the neonatal period in 19 (32.7%) patients. Multiple or recurrent invasive infections were observed in most survivors (n = 36/50, 72%).Clinical outcome was poor, with 24 deaths, in 10 cases during the first invasive episode and in 16 cases of invasive pneumococcal disease. However, no death and invasive infectious disease were reported in patients after the age of 8 years and 14 years, respectively. Antibiotic prophylaxis (n = 34), antipneumococcal vaccination (n = 31), and/or IgG infusion (n = 19), when instituted, had a beneficial impact on patients until the teenage years, with no seemingly detectable impact thereafter.IRAK-4 and MyD88 deficiencies predispose patients to recurrent life-threatening bacterial diseases, such as invasive pneumococcal disease in particular, in infancy and early childhood, with weak signs of inflammation. Patients and families should be informed of the risk of developing life-threatening infections; empiric antibacterial treatment and immediate medical consultation are strongly recommended in cases of suspected infection or moderate fever. Prophylactic measures in childhood are beneficial, until spontaneous improvement occurs in adolescenceen_US
dc.languageengen_US
dc.relation.ispartofMedicineen_US
dc.sourceMedicine[ISSN 0025-7974],v. 89, p. 403-425en_US
dc.subject32 Ciencias médicasen_US
dc.subject3205 Medicina internaen_US
dc.subject.otherInterleukin-1en_US
dc.subject.otherDisease Susceptibilityen_US
dc.subject.otherMyeloid Differentiation Factor 88en_US
dc.titleClinical features and outcome of patients with IRAK-4 and MyD88 deficiencyen_US
dc.typeinfo:eu-repo/semantics/reviewen_US
dc.typeArticleen_US
dc.identifier.doi10.1097/MD.0b013e3181fd8ec3en_US
dc.identifier.scopus78649358887-
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dc.description.lastpage425en_US
dc.description.firstpage403en_US
dc.relation.volume89en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Reseñaen_US
dc.description.numberofpages23en_US
dc.utils.revisionen_US
dc.date.coverdateNoviembre 2010en_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr4,256-
dc.description.jcrqQ1-
dc.description.scieSCIE-
item.fulltextSin texto completo-
item.grantfulltextnone-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-4344-8644-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameRodríguez Gallego, José Carlos-
Colección:Reseña
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