Clinical and Therapeutic Aspects of Sideroblastic Anaemia with B-Cell Immunodeficiency, Periodic Fever and Developmental Delay (SIFD) Syndrome: a Systematic Review Ilaria MaccoraAthimalaipet V. RamananGabriele Simonini CME Review Open access 19 August 2022 Pages: 1 - 30
Monitoring of Both Humoral and Cellular Immunities Could Early Predict COVID-19 Vaccine Efficacy Against the Different SARS-CoV2 Variants Manon VogrigAnne-Emmanuelle BergerStéphane Paul Original Article 25 August 2022 Pages: 31 - 45
Long-Term Antibody Response to SARS-CoV-2 in Children Gabor A. DunayMadalena Barrosothe C19.CHILD Study Group Original Article Open access 19 September 2022 Pages: 46 - 56
Immune Response to SARS-CoV-2 Infections in Children with Secondary Immunodeficiencies Karolina KuczborskaEwelina KrzemińskaJanusz Książyk Original Article Open access 23 September 2022 Pages: 57 - 64
Disseminated BCG Disease in a Patient with Hyper IgE Syndrome due to Dominant-Negative STAT3 Mutation—Case Report Luciano UrdinezVeronica GorisGarrahan Hospital Consortium Letter to Editor 29 August 2022 Pages: 65 - 68
A CDC42 Stop-loss Mutation in a Patient with Relapsing Polychondritis and Autoinflammation Rogier T. A. van WijckSigrid M. A. SwagemakersPaul L. A. van Daele Letter to Editor Open access 30 August 2022 Pages: 69 - 71
SGPL1 Deficiency: Nephrotic Syndrome with Lymphopenia Paulina TranMahnaz JameeKathleen E. Sullivan Letter to Editor 02 September 2022 Pages: 72 - 75
Severe Disseminated Mycobacterium kansasii Infection due to Autoantibodies Against IFN-ɣ Chun PanZhengbang DongHongsheng Wang Letter to Editor 03 September 2022 Pages: 76 - 79
TRECs/KRECs: Beyond the Diagnosis of Severe Combined Immunodeficiency Barbara Cristina RamosCarolina Sanchez ArandaAntonio Condino-Neto Letter to Editor 15 September 2022 Pages: 80 - 81
Wiskott Aldrich Syndrome-2 Caused by Novel Wiskott Aldrich Syndrome Protein–Interacting Protein (WIP) Deficiency Is Associated with Juvenile Myelomonocytic Leukaemia — a Case Report Srividhya SenthilAdrian J. ThrasherRobert F. Wynn Letter to Editor 28 September 2022 Pages: 82 - 84
Granulicatella adiacens Bacteremia in Chronic Granulomatous Disease Masashi OkaiTakashi IshikawaToshinao Kawai Letter to Editor 03 October 2022 Pages: 85 - 87
De Novo Somatic Mosaicism of CYBB Caused by Intronic LINE-1 Element Insertion Resulting in Chronic Granulomatous Disease Lang YuWenhui LiXiaodong Zhao Original Article 23 August 2022 Pages: 88 - 100
Improvement of Refractory Systemic Juvenile Idiopathic Arthritis-Associated Lung Disease with Single-Agent Blockade of IL-1β and IL-18 Julia E. RoodAyman RezkScott W. Canna Original Article 25 August 2022 Pages: 101 - 108
Inadequate Activation of γδT- and B-cells in Patient with Wiskott-Aldrich Syndrome (WAS) Portrayed by TRG and IGH Repertoire Analyses Dahlia PalevskiAmos SimonYu Nee Lee Original Article Open access 31 August 2022 Pages: 109 - 122
Mendelian Susceptibility to Mycobacterial Disease: Retrospective Clinical and Genetic Study in Mexico Ana Karen Peñafiel VicuñaMarco Yamazaki NakashimadaLizbeth Blancas Galicia Original Article 31 August 2022 Pages: 123 - 135
Three Adult Cases of STAT1 Gain-of-Function with Chronic Mucocutaneous Candidiasis Treated with JAK Inhibitors Emilie W. BorgströmMarie EdvinssonPeter Bergman Original Article Open access 02 September 2022 Pages: 136 - 150
Clinically Complex LRBA Deficiency Due to a Founder Allele in the Georgian Jewish Population Tal FreundSarah K. BaxterDavid Hagin Original Article 05 September 2022 Pages: 151 - 164
Novel Germline TET2 Mutations in Two Unrelated Patients with Autoimmune Lymphoproliferative Syndrome-Like Phenotype and Hematologic Malignancy Marta López-NevadoJavier Ortiz-MartínLuis M. Allende Original Article 06 September 2022 Pages: 165 - 180
Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited Vincent AllainVirginie GrandinEric Oksenhendler Original Article 26 September 2022 Pages: 181 - 191
Inherited IRAK-4 Deficiency in Acute Human Herpesvirus-6 Encephalitis Zeynep Güneş TepeYılmaz Yücehan YazıcıSerkan Belkaya Original Article 07 October 2022 Pages: 192 - 205
Current Transition Practice for Primary Immunodeficiencies and Autoinflammatory Diseases in Europe: a RITA-ERN Survey Muskan IsraniBethany NicholsonRITA-ERN Transition Working Group Consortium Original Article Open access 12 October 2022 Pages: 206 - 216
Delayed Diagnosis of Chronic Necrotizing Granulomatous Skin Lesions due to TAP2 Deficiency Ilad Alavi DarazamAtousa HakamifardDavood Mansouri Original Article 13 October 2022 Pages: 217 - 228
A Novel RAC2 Mutation Causing Combined Immunodeficiency Liang ZhangGe LvXiaodong Zhao OriginalPaper 03 October 2022 Pages: 229 - 240
Recurrent Infections in an Ethiopian Boy with Autosomal Recessive Major Histocompatibility Complex Type I Deficiency: a Case Report on a Very Rare Primary Immunodeficiency Disorder and a Review of Principles in Evaluation and Management Tinsae AlemayehuNetsanet Azene Gebeyehu Original Article 13 October 2022 Pages: 241 - 243
Correction to: Recurrent Infections in an Ethiopian Boy with Autosomal Recessive Major Histocompatibility Complex Type I Deficiency: a Case Report on a Very Rare Primary Immunodeficiency Disorder and a Review of Principles in Evaluation and Management Tinsae AlemayehuNetsanet Azene Gebeyehu Correction 17 November 2022 Pages: 244 - 244
Correction to: Protein‑losing Enteropathy as a Complication and/or Differential Diagnosis of Common Variable Immunodeficiency Sébastien SangesNicolas GermainGuillaume Lefèvre Correction 26 August 2022 Pages: 245 - 245