Clinical Features and Outcome of Patients With IRAK-4 and MyD88 Deficiency

被引:299
作者
Picard, Capucine [1 ,2 ,3 ]
von Bernuth, Horst [2 ,3 ,4 ]
Ghandil, Pegah [2 ,3 ,5 ]
Chrabieh, Maya [2 ,3 ]
Levy, Ofer [6 ,8 ,9 ]
Arkwright, Peter D. [10 ]
McDonald, Douglas [7 ,9 ]
Geha, Raif S. [7 ,9 ]
Takada, Hidetoshi [11 ]
Krause, Jens C. [12 ]
Creech, C. Buddy [12 ]
Ku, Cheng-Lung [2 ,3 ]
Ehl, Stephan [13 ]
Marodi, Laszlo [14 ]
Al-Muhsen, Saleh [5 ,15 ]
Al-Hajjar, Sami [5 ,15 ]
Al-Ghonaium, Abdulaziz [5 ,15 ]
Day-Good, Noorbibi K. [16 ]
Holland, Steven M. [17 ]
Gallin, John I. [17 ]
Chapel, Helen [18 ,19 ]
Speert, David P. [20 ]
Rodriguez-Gallego, Carlos [21 ]
Colino, Elena [22 ]
Garty, Ben-Zion [23 ]
Roifman, Chaim [24 ]
Hara, Toshiro [11 ]
Yoshikawa, Hideto [25 ]
Nonoyama, Shigeaki [26 ]
Domachowske, Joseph [27 ]
Issekutz, Andrew C. [28 ]
Tang, Mimi [29 ]
Smart, Joanne [29 ]
Zitnik, Simona Eva [30 ]
Hoarau, Cyrille [31 ]
Kumararatne, Dinakantha S. [32 ]
Thrasher, Adrian J. [33 ]
Davies, E. Graham [34 ]
Bethune, Claire [35 ]
Sirvent, Nicolas [36 ]
de Ricaud, Dominique [37 ]
Camcioglu, Yildiz [38 ]
Vasconcelos, Julia [39 ]
Guedes, Margarida [39 ]
Vitor, Artur Bonito [40 ]
Rodrigo, Carlos [41 ]
Almazan, Francisco [41 ]
Mendez, Maria [41 ]
Ignacio Arostegui, Juan [42 ]
Alsina, Laia [43 ]
机构
[1] Hop Necker Enfants Malad, AP HP, Study Ctr Primary Immunodeficiencies, Paris, France
[2] INSERM, U980, Lab Human Genet Infect Dis, Necker Branch, Paris, France
[3] Paris Descartes Univ, Paris, France
[4] Charite Hosp Humboldt Univ, Dept Pediat Pneumol & Immunol, Berlin, Germany
[5] King Saud Univ, Coll Med, Prince Naif Ctr Immunol Res, Riyadh 11461, Saudi Arabia
[6] Childrens Hosp, Div Infect Dis, Boston, MA 02115 USA
[7] Childrens Hosp, Div Immunol, Boston, MA 02115 USA
[8] Childrens Hosp Boston, Boston, MA 02115 USA
[9] Harvard Univ, Sch Med, Boston, MA USA
[10] Univ Manchester, Royal Manchester Childrens Hosp, Manchester, Lancs, England
[11] Kyushu Univ, Dept Pediat, Grad Sch Med Sci, Fukuoka 812, Japan
[12] Vanderbilt Univ, Dept Pediat, Div Pediat Infect Dis, Nashville, TN USA
[13] Univ Freiburg, Ctr Chron Immunodeficiency, Freiburg, Germany
[14] Univ Debrecen, Dept Infect & Pediat Immunol, Med & Hlth Sci Ctr, H-4012 Debrecen, Hungary
[15] King Faisal Specialist Hosp & Res Ctr, Dept Pediat, Riyadh 11211, Saudi Arabia
[16] Univ S Florida, Dept Pediat, Div Allergy & Immunol, St Petersburg, FL 33701 USA
[17] NIAID, Lab Clin Infect Dis, NIH, Bethesda, MD 20892 USA
[18] Univ Oxford, Oxford, England
[19] Oxford Radcliffe Hosp, Oxford, England
[20] Univ British Columbia, Dept Pediat, Div Infect & Immunol Dis, Vancouver, BC V6T 1W5, Canada
[21] Dr Negrin Univ Hosp Gran Canaria, Dept Immunol, Las Palmas Gran Canaria, Spain
[22] Insular Maternoinfantil Univ Hosp, Dept Pediat, Infect Dis Unit, Las Palmas Gran Canaria, Spain
[23] Schneider Childrens Med Ctr, Petah Tiqwa, Israel
[24] Univ Toronto, Hosp Sick Children, Dept Pediat, Div Immunol & Allergy, Toronto, ON M5G 1X8, Canada
[25] Miyagi Childrens Hosp, Dept Neurol, Sendai, Miyagi, Japan
[26] Natl Def Med Coll, Dept Pediat, Saitama, Japan
[27] SUNY Upstate Med Univ, Syracuse, NY USA
[28] Dalhousie Univ, Halifax, NS, Canada
[29] Royal Childrens Hosp, Parkville, Vic 3052, Australia
[30] Univ Children Hosp Ljubljana, Ljubljana, Slovenia
[31] CHU Tours, Unite Transversale Allergol Nephrol & Immunol Cli, Tours, France
[32] Addenbrookes Hosp, Dept Clin Biochem & Immunol, Cambridge, England
[33] Inst Child Hlth, Paediat Immunol & Mol Immunol Unit, London, England
[34] Great Ormond St Hosp Sick Children, Dept Clin Immunol, London, England
[35] Derriford Hosp, Dept Immunol, Plymouth PL6 8DH, Devon, England
[36] Univ Hosp Archet 2, Nice, France
[37] Childrens Hosp, Lenval Fdn, Nice, France
[38] Istanbul Univ, Cerrahpasa Med Sch, Istanbul, Turkey
[39] Gen Hosp Santo Antonio, Clin Pathol & Pediat Dept, Porto, Portugal
[40] Hosp Sao Joao, Dept Pediat, Porto, Portugal
[41] Autonomous Univ Barcelona, Hosp Germans Trias & Pujol, Dept Pediat, Barcelona, Spain
[42] Univ Barcelona, Immunol Dept CDB, Hosp Clin IDIBAPS, Barcelona, Spain
[43] Univ Barcelona, Dept Pediat, Hosp St Joan de Deu, Barcelona, Spain
[44] Univ Kinderspital Zurich, Dept Immunol, Zurich, Switzerland
[45] Catholic Univ Louvain, Expt Med Lab, Dept Med Diagnost Sci, Biomed Sci Grp, B-3000 Louvain, Belgium
[46] Rockefeller Univ, St Giles Lab Human Genet Infect Dis, Rockefeller Branch, New York, NY 10021 USA
[47] Hop Necker Enfants Malad, AP HP, Pediat Hematol Immunol Unit, Paris, France
关键词
PYOGENIC BACTERIAL-INFECTIONS; C-REACTIVE PROTEIN; KINASE-4; DEFICIENCY; PRIMARY IMMUNODEFICIENCIES; ECTODERMAL DYSPLASIA; ALPHA MUTATION; SIBLINGS; INNATE; IMMUNITY; INTERLEUKIN-1;
D O I
10.1097/MD.0b013e3181fd8ec3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:403 / 425
页数:23
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