Revisiting Human IL-12Rβ1 Deficiency

Ludovic de Beaucoudrey(Université Paris Cité), Arina Samarina, Jacinta Bustamante, Aurélie Cobat, Stéphanie Boisson‐Dupuis, Jacqueline Feinberg, Saleh Al‐Muhsen, Lucile Jannière, Y Rose, Maylis de Suremain, Xiao‐Fei Kong, Orchidée Filipe‐Santos, Ariane Chapgier, Capucine Pïcard, Alain Fischer, Figen Doğu, Aydan İkincioğulları, Gönül Tanır, Sami Al-Hajjar, Suliman Aljumaah, Husn H. Frayha, Zobaida Alsum, Sulaiman Al-Ajaji, Abdullah Alangari, Abdulaziz Al‐Ghonaium, Parisa Adimi, Davood Mansouri, Imen Ben‐Mustapha, Judith Yancoski, Ben‐Zion Garty, Carlos Rodríguez‐Gallego, Isabel Caragol, Necil Kütükçüler, Dinakantha Kumararatne, Smita Y. Patel, Rainer Döffinger, Andrew Exley, Olle Jeppsson, Janine Reichenbach, David Nadal, Yaryna Boyko, Barbara Pietrucha, Suzanne T. Anderson, Michael Levin, Liliane Schandené, Kinda Schepers, André Efira, Françoise Mascart, Masao Matsuoka, Tatsunori Sakai, Claire‐Anne Siegrist, Klára Frecerová, Renate Blüetters-Sawatzki, Jutta Bernhöft, Joachim Freihorst, Ulrich Baumann, Darko Richter, Filomeen Haerynck, Frans De Baets, Vas Novelli, David A. Lammas, Christiane Vermylen, David Tuerlinckx, Chris Nieuwhof, Małgorzata Pac, W. Haas, Ingrid Müller‐Fleckenstein, Bernhard Fleckenstein, Jacob Levy, Revathi Raj, Aileen Cleary Cohen, David B. Lewis, Steven M. Holland, Kuender D. Yang, Xiaochuan Wang, Xiaohong Wang, Liping Jiang, Xiqiang Yang, Chaomin Zhu, Yuanyuan Xie, Pamela Lee, Koon Wing Chan, Tong‐Xin Chen, Gabriela Castro, Ivelisse Natera, Ana Codoceo, Alejandra King, Liliana Bezrodnik, Daniela Di Giovani, María Isabel Gaillard, Dewton de Moraes Vasconcelos, Anete Sevciovic Grumach, Alberto José da Silva Duarte, Ruth Aldana, Francisco Espinosa‐Rosales, Mohammed Bejaoui, Ahmed Aziz Bousfiha, Jamila El Baghdadi, Namık Yaşar Özbek, Güzide Aksu, Melike Keser, Ayper Somer, Nevin Hatipoğlu, Çiğdem Aydoğmuş, Suna Asi̇lsoy, Yıldız Çamcıoğlu, Saniye Gülle, Tuba Turul Özgür, Meteran Ozen, Matías Oleastro, Andrea Bernasconi, Setareh Mamishi, Nima Parvaneh, Sergio D. Rosenzweig, Mohamed‐Ridha Barbouche, Sigifredo Pedraza‐Sánchez, YL Lau, Mohammad Ehlayel, Claire Fieschi, Laurent Abel, Özden Sanal, Jean‐Laurent Casanova
Medicine
November 1, 2010
Cited by 385Open Access
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Abstract

Interleukin-12 receptor β1 (IL-12Rβ1) deficiency is the most common form of Mendelian susceptibility to mycobacterial disease (MSMD). We undertook an international survey of 141 patients from 102 kindreds in 30 countries. Among 102 probands, the first infection occurred at a mean age of 2.4 years. In 78 patients, this infection was caused by Bacille Calmette-Guérin (BCG; n = 65), environmental mycobacteria (EM; also known as atypical or nontuberculous mycobacteria) (n = 9) or Mycobacterium tuberculosis (n = 4). Twenty-two of the remaining 24 probands initially presented with nontyphoidal, extraintestinal salmonellosis. Twenty of the 29 genetically affected sibs displayed clinical signs (69%); however 8 remained asymptomatic (27%). Nine nongenotyped sibs with symptoms died. Recurrent BCG infection was diagnosed in 15 cases, recurrent EM in 3 cases, recurrent salmonellosis in 22 patients. Ninety of the 132 symptomatic patients had infections with a single microorganism. Multiple infections were diagnosed in 40 cases, with combined mycobacteriosis and salmonellosis in 36 individuals. BCG disease strongly protected against subsequent EM disease (p = 0.00008). Various other infectious diseases occurred, albeit each rarely, yet candidiasis was reported in 33 of the patients (23%). Ninety-nine patients (70%) survived, with a mean age at last follow-up visit of 12.7 years ± 9.8 years (range, 0.5-46.4 yr). IL-12Rβ1 deficiency is characterized by childhood-onset mycobacteriosis and salmonellosis, rare recurrences of mycobacterial disease, and more frequent recurrence of salmonellosis. The condition has higher clinical penetrance, broader susceptibility to infections, and less favorable outcome than previously thought. Abbreviations: BCG = Bacille Calmette-Guérin, CI = confidence interval, EBV-B cell lines = Epstein-Barr virus-transformed lymphoblastoid cell lines, ELISA = enzyme-linked immunosorbent assay, EM= environmental mycobacteria (nontuberculous mycobacteria), FBS = fetal bovine serum, FD = fibronectin domain, IFNGR = interferon-γ receptor, IL12B = interleukin-12B, IL-12Rβ1 = interleukin-12 receptor beta 1 chain, MSMD = Mendelian susceptibility tomycobacterial disease, NEMO = nuclear factor-κB essential modulator, PBS = phosphate-buffered saline, PCR = polymerase chain reaction, PHA = phytohemagglutinin, PR = present report, STAT1 = Signal transducer and activator of transcription 1.


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