Issue 3/2021
Content (27 Articles)
STING-Mediated Lung Inflammation and Beyond
Marie-Louise Frémond, Yanick J. Crow
SARS-CoV-2-Induced ARDS Associates with MDSC Expansion, Lymphocyte Dysfunction, and Arginine Shortage
Florian Reizine, Mathieu Lesouhaitier, Murielle Gregoire, Kieran Pinceaux, Arnaud Gacouin, Adel Maamar, Benoit Painvin, Christophe Camus, Yves Le Tulzo, Pierre Tattevin, Matthieu Revest, Audrey Le Bot, Alice Ballerie, Berengère Cador-Rousseau, Mathieu Lederlin, Thomas Lebouvier, Yoann Launey, Maelle Latour, Clotilde Verdy, Delphine Rossille, Simon Le Gallou, Joelle Dulong, Caroline Moreau, Claude Bendavid, Mikael Roussel, Michel Cogne, Karin Tarte, Jean-Marc Tadié
Distinctive Features of Kawasaki Disease Following SARS-CoV-2 Infection: a Controlled Study in Paris, France
Julie Toubiana, Jérémie F. Cohen, Joséphine Brice, Clément Poirault, Fanny Bajolle, William Curtis, Florence Moulin, Soraya Matczak, Marianne Leruez, Jean-Laurent Casanova, Martin Chalumeau, Melissa Taylor, Slimane Allali
Plasma Exchange to Rescue Patients with Autoantibodies Against Type I Interferons and Life-Threatening COVID-19 Pneumonia
Nicolas de Prost, Paul Bastard, Romain Arrestier, Slim Fourati, Mathieu Mahévas, Sonia Burrel, Karim Dorgham, Guy Gorochov, Yacine Tandjaoui-Lambiotte, Iname Azzaoui, Ignacio Fernandes, Alain Combes, Jean-Laurent Casanova, Armand Mekontso-Dessap, Charles-Edouard Luyt
Central Nervous System Histoplasma-Associated Post-infectious Inflammatory Response Syndrome (Histo-PIIRS)
Owen Dean, Seher Anjum, Bryan Hess, Dima A. Hammoud, Deena Athas, Joseph Wheat, Peter R. Williamson
Liver Abscess in Chronic Granulomatous Disease—Two Decades of Experience from a Tertiary Care Centre in North-West India
Rakesh Kumar Pilania, Amit Rawat, Pandiarajan Vignesh, Sandesh Guleria, Ankur Kumar Jindal, Gargi Das, Deepti Suri, Anju Gupta, Kirti Gupta, Koon-Wing Chan, Yu-Lung Lau, Kohsuke Imai, Surjit Singh
Serum Sp17 Autoantibody Serves as a Potential Specific Biomarker in Patients with SAPHO Syndrome
Hongqin You, Guanglei Dang, Bichao Lu, Siya Zhang, Chen Li, Lun Wang, Yu Hu, Hui Chen, Jianmin Zhang, Wei He
An Unusual Pattern of Premature Cervical Spine Degeneration in STAT3-LOF
Amelia L. Mitchell, Amanda K. Urban, Alexandra F. Freeman, Dima A. Hammoud
Use of Complementary and Alternative Medicine in Patients with Primary Immunodeficiency: a Multicentric Analysis of 101 Patients
Anna S. Harasim, Manuel Krone, Hans-Peter Tony, Micha Gawlik, Torsten Witte, Stefanie Joos, Michael Gernert, Marc Schmalzing, Henner Morbach, Eva C. Schwaneck
Newborn Screening for Severe Combined Immunodeficiency: 10-Year Experience at a Single Referral Center (2009–2018)
Julia Thorsen, Kayla Kolbert, Avni Joshi, Mei Baker, Christine M. Seroogy
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies
Lorenzo Lodi, Isabelle Melki, Vincent Bondet, Luis Seabra, Gillian I. Rice, Edwin Carter, Alice Lepelley, Maria José Martin-Niclós, Buthaina Al Adba, Brigitte Bader-Meunier, Magalie Barth, Thomas Blauwblomme, Christine Bodemer, Odile Boespflug-Tanguy, Russel C. Dale, Isabelle Desguerre, Camille Ducrocq, Fabienne Dulieu, Cécile Dumaine, Pierre Ellul, Alice Hadchouel, Véronique Hentgen, Miguel Hié, Marie Hully, Eric Jeziorski, Romain Lévy, Fanny Mochel, Simona Orcesi, Sandrine Passemard, Marie Pouletty, Pierre Quartier, Florence Renaldo, Rainer Seidl, Jay Shetty, Bénédicte Neven, Stéphane Blanche, Darragh Duffy, Yanick J. Crow, Marie-Louise Frémond
Characterization of Infants with Idiopathic Transient and Persistent T Cell Lymphopenia Identified by Newborn Screening—a Single-Center Experience in New York State
Artemio M. Jongco III, Robert Sporter, Elise Hon, Omer Elshaigi, Shouling Zhang, Foysal Daian, Emily Bae, Amanda Innamorato, Catherine Capo, Brianne Navetta-Modrov, David W. Rosenthal, Vincent R. Bonagura
TREC Screening for WHIM Syndrome
Martin Oman Evans II, Maureen M. Petersen, Amer Khojah, Soma C. Jyonouchi, George S. Edwardson, Yasmin West Khan, James Albert Connelly, David Morris, Shamik Majumdar, David H. McDermott, Jolan E. Walter, Philip M. Murphy
Correction to: TREC Screening for WHIM Syndrome
Martin Oman Evans II, Maureen M. Petersen, Amer Khojah, Soma C. Jyonouchi, George S. Edwardson, Yasmin West Khan, James Albert Connelly, David Morris, Shamik Majumdar, David H. McDermott, Jolan E. Walter, Philip M. Murphy
Clinical and Immunological Features of 96 Moroccan Children with SCID Phenotype: Two Decades’ Experience
Ibtihal Benhsaien, Fatima Ailal, Jalila El Bakkouri, Leïla Jeddane, Hind Ouair, Brahim Admou, Mohamed Bouskraoui, Mohamed Hbibi, Mustapha Hida, Naïma Amenzoui, Zineb Jouhadi, Naïma El Hafidi, Nouredine Rada, Noufissa Benajiba, Rachid Abilkassem, Abdallah Badou, Ahmed Aziz Bousfiha
Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance
Carmen Oleaga-Quintas, Edgar Borges de Oliveira-Júnior, Jérémie Rosain, Franck Rapaport, Caroline Deswarte, Antoine Guérin, Sairaj Munavar Sajjath, Yu Jerry Zhou, Stéphane Marot, Claire Lozano, Lidia Branco, Nuria Fernández-Hidalgo, Dukhee Betty Lew, Anne-Sophie Brunel, Caroline Thomas, Elise Launay, Andrés Augusto Arias, Alexis Cuffel, Vanesa Cunill Monjo, Anna-Lena Neehus, Laura Marques, Manon Roynard, Marcela Moncada-Vélez, Bengü Gerçeker, Roger Colobran, Marie-Gabrielle Vigué, Gabriela Lopez-Herrera, Laura Berron-Ruiz, Nora Hilda Segura Méndez, Patricia O’Farrill Romanillos, Tom Le Voyer, Anne Puel, Christine Bellanné-Chantelot, Kacy A. Ramirez, Lazaro Lorenzo-Diaz, Noé Ramirez Alejo, Rebeca Pérez de Diego, Antonio Condino-Neto, Fethi Mellouli, Carlos Rodriguez-Gallego, Torsten Witte, José Franco Restrepo, Mariana Jobim, Stéphanie Boisson-Dupuis, Eric Jeziorski, Claire Fieschi, Guillaume Vogt, Jean Donadieu, Marlène Pasquet, Julia Vasconcelos, Fatma Omur Ardeniz, Mónica Martínez-Gallo, Regis A. Campos, Luiz Fernando Jobim, Rubén Martínez-Barricarte, Kang Liu, Aurélie Cobat, Laurent Abel, Jean-Laurent Casanova, Jacinta Bustamante
Biomarkers for Early Diagnosis of Hemophagocytic Lymphohistiocytosis in Critically Ill Patients
France Debaugnies, Bhavna Mahadeb, Carole Nagant, Nathalie Meuleman, David De Bels, Fleur Wolff, Philippe Gottignies, Adriano Salaroli, Patricia Borde, Michel Voué, Francis Corazza
The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
Stuart G. Tangye, Waleed Al-Herz, Aziz Bousfiha, Charlotte Cunningham-Rundles, Jose Luis Franco, Steven M Holland, Christoph Klein, Tomohiro Morio, Eric Oksenhendler, Capucine Picard, Anne Puel, Jennifer Puck, Mikko R. J. Seppänen, Raz Somech, Helen C Su, Kathleen E. Sullivan, Troy R. Torgerson, Isabelle Meyts
Uncontrolled Epstein-Barr Virus as an Atypical Presentation of Deficiency in ADA2 (DADA2)
Joel P. Brooks, Andrew J. Rice, Weizhen Ji, Stephen M. Lanahan, Monica Konstantino, Jasmeen Dara, Michael S. Hershfield, Amy Cruickshank, Elif Dokmeci, Saquib Lakhani, Carrie L. Lucas
Successful Hematopoietic Stem Cell Transplantation for Autosomal Recessive STAT1 Complete Deficiency
Shuhei Karakawa, Maiko Shimomura, Sonoko Sakata, Tadashi Matsubayashi, Satoshi Okada
Benralizumab in Severe and Refractory PDGFRA-Negative Hypereosinophilic Syndrome
Iolanda Alen Coutinho, Frederico S. Regateiro, Carlos Loureiro, Ana Todo-Bom
Chronic Disseminated Gonococcal Infection in a Japanese Man with Novel C5 Gene Mutation
Kazuhiko Ikeuchi, Koh Okamoto, Norimitsu Inoue, Shu Okugawa, Kyoji Moriya
Soluble Interleukin-2 Receptor Is a Promising Serum Biomarker for Granulomatous Disease in Common Variable Immune Deficiency
Astrid C. van Stigt, Virgil A. S. H. Dalm, Nicole M. A. Nagtzaam, Damian A. van Rijswijk, Barbara H. Barendregt, P. Martin van Hagen, Hanna IJspeert, Willem A. Dik
Pediatric Demodicosis Associated with Gain-of-Function Variant in STAT1 Presenting as Rosacea-Type Rash
Bouchra Baghad, Fatima Zahra El Fatoiki, Ibtihal Benhsaien, Ahmed Aziz Bousfiha, Anne Puel, Mélanie Migaud, Soumiya Chiheb, Fatima Ailal
Novel IL36RN Mutation Identified in Pediatric-Onset Generalized Pustular Psoriasis Causes IL36 Antagonist Degradation
Hongmei Li, Dan Liao, Shasha Meng, Jingru Liu, Songyang Li, Sili Ni, Yunfei Xu, Yong Zhao, Weihui Zhou
Inflammatory Pseudotumor of Liver and Budd-Chiari Syndrome: a Tale During 10 Years of Follow-up in a Child with Severe Congenital Neutropenia
Kiruthiga Sugumar, Jaikumar Govindaswamy Ramamoorthy, Avinash Anantharaj, Nirmalkumar Baalakumar, Pradeep Kumar Sankar
Clinical and Immunological Analyses of Ten Patients with MIRAGE Syndrome
Kanako Mitsui-Sekinaka, Satoshi Narumi, Yujin Sekinaka, Kenji Uematsu, Yusuke Yoshida, Naoko Amano, Hirohito Shima, Tomonobu Hasegawa, Shigeaki Nonoyama