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http://hdl.handle.net/10553/48631
Título: | Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency | Autores/as: | Picard, Capucine Von Bernuth, Horst Ghandil, Pegah Chrabieh, Maya Levy, Ofer Arkwright, Peter D. McDonald, Douglas Geha, Raif S. Takada, Hidetoshi Krause, Jens C. Creech, C. Buddy Ku, Cheng Lung Ehl, Stephan Maródi, László Al-Muhsen, Saleh Al-Hajjar, Sami Al-Ghonaium, Abdulaziz Day-Good, Noorbibi K. Holland, Steven M. Gallin, John I. Chapel, Helen Speert, David P. Rodriguez-Gallego, Carlos Colino, Elena Garty, Ben Zion Roifman, Chaim Hara, Toshiro Yoshikawa, Hideto Nonoyama, Shigeaki Domachowske, Joseph Issekutz, Andrew C. Tang, Mimi Smart, Joanne Zitnik, Simona Eva Hoarau, Cyrille Kumararatne, Dinakantha S. Thrasher, Adrian J. Davies, E. Graham Bethune, Claire Sirvent, Nicolas De Ricaud, Dominique Camcioglu, Yildiz Vasconcelos, Júlia Guedes, Margarida Vitor, Artur Bonito Rodrigo, Carlos Almazán, Francisco Méndez, Maria Aróstegui, Juan Ignacio Alsina, Laia Fortuny, Claudia Reichenbach, Janine Verbsky, James W. Bossuyt, Xavier Doffinger, Rainer Abel, Laurent Puel, Anne Casanova, Jean Laurent |
Clasificación UNESCO: | 32 Ciencias médicas 3205 Medicina interna |
Palabras clave: | Interleukin-1 Disease Susceptibility Myeloid Differentiation Factor 88 |
Fecha de publicación: | 2010 | Publicación seriada: | Medicine | Resumen: | Autosomal 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 adolescence | URI: | http://hdl.handle.net/10553/48631 | ISSN: | 0025-7974 | DOI: | 10.1097/MD.0b013e3181fd8ec3 | Fuente: | Medicine[ISSN 0025-7974],v. 89, p. 403-425 |
Colección: | Reseña |
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