Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development Peter J. MustilloKathleen E. SullivanM. Louise Markert How I Manage Open access 17 January 2023 Pages: 247 - 270
COVID-19 Vaccination Responses with Different Vaccine Platforms in Patients with Inborn Errors of Immunity Lorenzo ErraIgnacio UriarteMaría Belén Almejun Original Article 17 October 2022 Pages: 271 - 285
Combination of WFDC2, CHI3L1, and KRT19 in Plasma Defines a Clinically Useful Molecular Phenotype Associated with Prognosis in Critically Ill COVID-19 Patients Takeshi EbiharaTsunehiro MatsubaraHiroshi Ogura Original Article Open access 04 November 2022 Pages: 286 - 298
Safety of mRNA COVID-19 Vaccines in Patients with Inborn Errors of Immunity: an Italian Multicentric Study Cinzia MilitoFrancesco CinettoDavide Firinu Original Article Open access 14 November 2022 Pages: 299 - 307
Serving Underserved Patients with Primary Immune Deficiency Disorders: A Pilot Educational Program for Clinical Fellows Jessica Galant-SwaffordElizabeth GeorgeAnna Meyer Letter to Editor 13 October 2022 Pages: 308 - 311
Germline Variant Interpretation in Children with Severe Sepsis Benjamin T. PrinceElizabeth A. VargaKim L. McBride Letter to Editor 29 October 2022 Pages: 312 - 314
MAGT1 Gene Mutation is Associated with Myositis and CD127 Expression Downregulation Sheng ChenXuan WangJie Lin Letter to Editor 04 November 2022 Pages: 315 - 318
Disseminated Acanthamoeba Infection in a Bone Marrow Transplant Recipient with CTLA-4 Haploinsufficiency Fatima Al DhaheriNicole GunasekeraSadaf Hussain Letter to Editor 07 November 2022 Pages: 319 - 322
CD40LG Triplication Associates with Immune Dysregulation and Exhaustion Wenny SantaniemiNora PernaaCD40L consortium Letter to Editor 08 November 2022 Pages: 323 - 326
Functional STAT3 Deficiency from Co-Localization with SMAD2/3 Can Account for Infective Predisposition and Hyper IgE-like Manifestation in Loeys-Dietz Syndrome Sharada RavikumarAseervatham Anusha AmaliLouis Yi Ann Chai Letter to Editor 09 November 2022 Pages: 327 - 330
SPENCD Presenting with Evans Phenotype and Clinical Response to JAK1/2 Inhibitors—a Report of 2 Cases Akshaya ChougulePrasad TaurMukesh M. Desai Letter to Editor 14 November 2022 Pages: 331 - 334
B-cell Immunodeficiency in a Patient with Pearson Syndrome Yu-Chia ChenShiann-Tarng JouHsin-Hui Yu Letter to Editor 15 November 2022 Pages: 335 - 337
Genotype and Phenotype of Adenosine Deaminase 2 Deficiency: a Report from Saudi Arabia Fahad AlabbasTalal AlanziAbdulrahman Alsultan Original Article 14 October 2022 Pages: 338 - 349
Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency Odeya DavidEyal KristalAmit Nahum Original Article 18 October 2022 Pages: 350 - 357
Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling Elina A. TuovinenSakari PöystiJuha Grönholm Original Article Open access 19 October 2022 Pages: 358 - 370
Interferon-Driven Immune Dysregulation in Common Variable Immunodeficiency–Associated Villous Atrophy and Norovirus Infection Valentina StrohmeierGeoffroy AndrieuxKlaus Warnatz Original Article Open access 25 October 2022 Pages: 371 - 390
CVID-Associated B Cell Activating Factor Receptor Variants Change Receptor Oligomerization, Ligand Binding, and Signaling Responses Violeta BlockEirini SevdaliHermann Eibel Original Article Open access 29 October 2022 Pages: 391 - 405
Fulminant Viral Hepatitis in Two Siblings with Inherited IL-10RB Deficiency Cecilia B. KorolSerkan BelkayaEmmanuelle Jouanguy Original Article Open access 29 October 2022 Pages: 406 - 420
IRAK1 Duplication in MECP2 Duplication Syndrome Does Not Increase Canonical NF-κB–Induced Inflammation Ilona GottschalkUwe KölschHorst von Bernuth Original Article Open access 02 November 2022 Pages: 421 - 439
Lentiviral Gene Transfer Corrects Immune Abnormalities in XIAP Deficiency Joseph TopalNeelam PanchalClaire Booth Original Article Open access 03 November 2022 Pages: 440 - 451
Genetic Causes, Clinical Features, and Survival of Underlying Inborn Errors of Immunity in Omani Patients: a Single-Center Study Salem Al-TamemiShoaib Al-ZadjaliDavid Dennison Original Article 03 November 2022 Pages: 452 - 465
Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases Rintaro OnoMiyuki TsumuraHirokazu Kanegane Original Article 07 November 2022 Pages: 466 - 478
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia Farrukh SheikhHuda AlajlanAnas M. Alazami Original Article 08 November 2022 Pages: 479 - 484
Genetic Diagnosis of Inborn Errors of Immunity in an Emerging Country: a Retrospective Study of 216 Moroccan Patients Abderrahmane MoundirHind OuairAhmed Aziz Bousfiha Original Article 11 November 2022 Pages: 485 - 494
Pathogenic Interleukin-10 Receptor Alpha Variants in Humans — Balancing Natural Selection and Clinical Implications Dominik AschenbrennerZiqing YeHolm H. Uhlig Original Article Open access 12 November 2022 Pages: 495 - 511
A Heterozygous Gain-of-Function Variant in IKBKB Associated with Autoimmunity and Autoinflammation Keith SaccoHye Sun KuehnMichael D. Keller Original Article 15 November 2022 Pages: 512 - 520