Ausgabe 4/2021
Inhalt (22 Artikel)
Personalized IgG Replacement Therapy for Patients with B cell Inborn Errors of Immunity
Vincent R. Bonagura
Genetic Mosaicism as a Cause of Inborn Errors of Immunity
Jahnavi Aluri, Megan A. Cooper
C1 Esterase Inhibition: Targeting Multiple Systems in COVID-19
T. M. Ayodele Adesanya, Courtney M. Campbell, Lijun Cheng, Princess U. Ogbogu, Rami Kahwash
The Impact of the SARS-CoV-2 Pandemic in PID Patients Receiving Ig Replacement Therapy
Sukru Cekic, Fatih Cicek, Sara Sebnem Kilic
Cytokine Profiles Before and After Immune Modulation in Hospitalized Patients with COVID-19
Veronica Azmy, Kelsey Kaman, Daiwei Tang, Hongyu Zhao, Charles Dela Cruz, Jeffrey E. Topal, Maricar Malinis, Christina C. Price
Failure of Viral-Specific T Cells Administered in Pre-transplant Settings in Children with Inborn Errors of Immunity
Laura Alonso, Ana Méndez-Echevarría, Francesc Rudilla, Yasmina Mozo, Pere Soler-Palacin, Luisa Sisinni, David Bueno, Jacques Riviere, Raquel de Paz, Elena Sánchez-Zapardiel, Sergi Querol, Rebeca Rodriguez-Pena, Eduardo López-Granados, Ramón Gimeno, Cristina Díaz de Heredia, Antonio Pérez-Martínez
Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
Giuliana Giardino, Svetlana O. Sharapova, Peter Ciznar, Fatima Dhalla, Luca Maragliano, Akella Radha Rama Devi, Candan Islamoglu, Aydan Ikinciogullari, Sule Haskologlu, Figen Dogu, Rima Hanna-Wakim, Ghassan Dbaibo, Janet Chou, Emilia Cirillo, Carla Borzacchiello, Alexandra Y. Kreins, Austen Worth, Ioanna A. Rota, José G. Marques, Muge Sayitoglu, Sinem Firtina, Moaffaq Mahdi, Raif Geha, Bénédicte Neven, Ana E. Sousa, Fabio Benfenati, Georg A. Hollander, E. Graham Davies, Claudio Pignata
Stepwise Reversal of Immune Dysregulation Due to STAT1 Gain-of-Function Mutation Following Ruxolitinib Bridge Therapy and Transplantation
Basak Kayaoglu, Nurhan Kasap, Naz Surucu Yilmaz, Louis Marie Charbonnier, Busranur Geckin, Arzu Akcay, Sevgi Bilgic Eltan, Gulyuz Ozturk, Ahmet Ozen, Elif Karakoc-Aydiner, Talal A. Chatila, Mayda Gursel, Safa Baris
Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3
Kay Tanita, Fumiaki Sakura, Ryusuke Nambu, Miyuki Tsumura, Yusuke Imanaka, Hidenori Ohnishi, Zenichiro Kato, Jie Pan, Akihiro Hoshino, Koji Suzuki, Motoko Yasutomi, Shuichiro Umetsu, Chizuru Okada, Masatoshi Takagi, Kohsuke Imai, Osamu Ohara, Alexo M. Muise, Satoshi Okada, Tomohiro Morio, Hirokazu Kanegane
Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3
Kay Tanita, Fumiaki Sakura, Ryusuke Nambu, Miyuki Tsumura, Yusuke Imanaka, Hidenori Ohnishi, Zenichiro Kato, Jie Pan, Akihiro Hoshino, Koji Suzuki, Motoko Yasutomi, Shuichiro Umetsu, Chizuru Okada, Masatoshi Takagi, Kohsuke Imai, Osamu Ohara, Alexo M. Muise, Satoshi Okada, Tomohiro Morio, Hirokazu Kanegane
Infectious Complications Predict Premature CD8+ T-cell Senescence in CD40 Ligand-Deficient Patients
Junghee J. Shin, Jason Catanzaro, Jennifer R. Yonkof, Ottavia Delmonte, Keith Sacco, Min Sun Shin, Srikar Reddy, Paula J. Whittington, Gary Soffer, Peter J. Mustillo, Kathleen E. Sullivan, Luigi D. Notarangelo, Roshini S. Abraham, Neil Romberg, Insoo Kang
Life-Saving, Dose-Adjusted, Targeted Therapy in a Patient with a STAT3 Gain-of-Function Mutation
Eytan Sarfati, Jérome Hadjadj, Mathieu Fusaro, Roman Klifa, Marion Grimaud, Laureline Berteloot, Alice Hadchouel, Cécile Godot, Marie-Claude Stolzenberg, Marie-Louise Frémond, Claire Pressiat, Thierry Molina, Alain Fischer, Capucine Picard, Sylvain Renolleau, Frederic Rieux-Laucat, Stephane Blanche, Benedicte Neven
The First Case of BENTA Disease (B Cell Expansion with NF-κB and T Cell Anergy) from Iran
Maryam Neishabury, Azita Azarkeivan, Maghsood Mehri, Hossein Najmabadi, Taher Cheraghi
Aspergillus fumigatus Skull Bone Osteomyelitis and Native Valve Endocarditis in a Young Boy: an Unusual Presentation of Chronic Granulomatous Disease
Gummadi Anjani, Ankur Kumar Jindal, Ashwini Prithvi, Harsimran Kaur, Madhubala Sharma, Sanjeev Naganur, Pandiarajan Vignesh, Amit Rawat, Surjit Singh
Inherited TOP2B Mutation: Possible Confirmation of Mutational Hotspots in the TOPRIM Domain
Melinda Erdős, Árpád Lányi, György Balázs, Jean-Laurent Casanova, Bertrand Boisson, László Maródi
Successful Haploidentical Transplant Using Post-Transplant Cyclophosphamide in a Child with Chronic Granulomatous Disease—First Report from the Indian Subcontinent
Sagar Bhattad, Commondoor Padmanabhan Raghuram, Fulvio Porta, Stalin Ramprakash
X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase
Nourhen Agrebi, Giusy Gentilcore, Jean-Charles Grivel, Ghroob Alkhayer, Jihad Hassoun, Amel Hassan, Mehdi Adeli, Bernice Lo
Generalized Pustular Psoriasis in Patients with Interferon Gamma (IFN-γ) Receptor Deficiency and Mycobacterial Infection
Haijuan Xiao, Xin Guo, Bing Hu, Jinrong Liu, Shunying Zhao, Zhe Xu, Nan Zhang, Lejian He, Yan Liu, Linlin Liu, Shaoying Li, Wei Li, Gang Liu
Complete IFN-γR1 Deficiency in a Boy Due to UPD(6)mat with IFNGR1 Novel Splicing Variant
Ping Zhang, Wenjing Ying, Bingbing Wu, Renchao Liu, Huijun Wang, Xiaochuan Wang, Yulan Lu
Novel ADA2 Compound Heterozygous Mutations Resulting in Deficiency of Adenosine Deaminase 2 in a Pair of Siblings
Li Guo, Jun Wang, Xinghui Yang, Rongjun Zheng, Natalie Deuitch, Panfeng Tao, Qing Zhou
Toxoplasmosis-Associated Hemophagocytic Lymphohistiocytosis in Allogeneic Transplantation
Ilaria Cutini, Antonella Gozzini, Chiara Nozzoli, Riccardo Boncompagni, Chiara Innocenti, Arianna Fani, Riccardo Saccardi
Correction to: Helicobacter cinaedi-Associated Refractory Cellulitis in Patients with X-Linked Agammaglobulinemia
Kento Inoue, Saeko Sasaki, Takahiro Yasumi, Kohsuke Imai, Takashi Kusunoki, Tomohiro Morio, Hirokazu Kanegane