2024

          Rosain et al., Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases. The Journal of Experimental Medicine. 2024

          Arango-Franco et al., IL-7–dependent and –independent lineages of IL-7R–dependent human T cells. Journal of Clinical Investigation. 2024

          Bougarn et al., Concomitant Ultrarare Mutations in TLR3 and CTPS2 in a Patient with Severe and Recurrent Respiratory Infections in Early Life. Journal of Clinical Immunology. 2024



          Momenilandi et al., FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice. Cell. 2024

          Guérin et al., Helper T cell immunity in humans with inherited CD4 deficiency. The Journal of Experimental Medicine. 2024

          Materna et al., The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants. Science. 2024

          Rosain et al., Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency. Journal of Clinical Immunology. 2024

          Bastard et al., Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children. The Journal of Experimental Medicine. 2024


    2023

          Benezech et al., Pre–Covid-19, SARS-CoV-2–Negative Multisystem Inflammatory Syndrome in Children. New England Journal of Medicine. 2023

          Bohlen et al., Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria. Cell. 2023

          Khan et al., Associations between HLA class II alleles and IgE sensitization to allergens in the Qatar Biobank cohort. Journal of Allergy and Clinical Immunology Global. 2023

          Ali et al., Organizing training workshops on gene literature retrieval, profiling, and visualization for early career researchers. F1000Research. 2023

          Liu et al., Encephalitis and poor neuronal death–mediated control of herpes simplex virus in human inherited RIPK3 deficiency. Science Immunology. 2023

          Massa et al., Interferons and Resistance Mechanisms in Tumors and Pathogen-Driven Diseases—Focus on the Major Histocompatibility Complex (MHC) Antigen Processing Pathway. International Journal of Molecular Sciences. 2023

          Philippot et al., Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria. Science Immunology. 2023


    2022

          Lévy et al., Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency. The Journal of Experimental Medicine. 2022

          Ogishi et al., Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis. The Journal of Experimental Medicine. 2022

          Nasrallah et al., Detection of Antinuclear Antibodies Targeting Intracellular Signal Transduction, Metabolism, Apoptotic Processes and Cell Death in Critical COVID-19 Patients. Mediterranean Journal of Hematology and Infectious Diseases. 2022

          Ogishi et al., Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency. The Journal of Experimental Medicine. 2022

          Khan et al., Human leukocyte antigen class II gene diversity tunes antibody repertoires to common pathogens. Frontiers in Immunology. 2022

          Campbell et al., Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency. The Journal of Experimental Medicine. 2022


          Abolhassani et al., Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome. Journal of Clinical Immunology. 2022

    2021

          Lévy et al., Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents. Journal of Clinical Investigation. 2021

          Guennoun et al., A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes. Journal of Clinical Immunology. 2021

          Asano et al., X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19. Science Immunology. 2021

          Béziat et al., Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy. Cell. 2021

          Voyer et al., Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency. The Journal of Immunology. 2021


          Asano et al., Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance. The Journal of Experimental Medicine. 2021

          Voyer et al., Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease. Proceedings of the National Academy of Sciences. 2021

          Chouchane et al., Dromedary camels as a natural source of neutralizing nanobodies against SARS-CoV-2. JCI Insight. 2021

          Hasan et al., Virome-wide serological profiling reveals association of herpesviruses with obesity. Scientific Reports. 2021

          Khan et al., Distinct antibody repertoires against endemic human coronaviruses in children and adults. JCI Insight. 2021

          Bastard et al., Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency. Journal of Clinical Investigation. 2021

    2020



          Kerner et al., Inherited human IFN-γ deficiency underlies mycobacterial disease. Journal of Clinical Investigation. 2020

          Drutman et al., Fatal Cytomegalovirus Infection in an Adult with Inherited NOS2 Deficiency. New England Journal of Medicine. 2020

    2019

          Li et al., Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β. Science Immunology. 2019

          Bougarn et al., A curated transcriptome dataset collection to investigate inborn errors of immunity. F1000Research. 2019

          Khourieh et al., A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance. Proceedings of the National Academy of Sciences. 2019

          Melki et al., Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines. The Journal of Experimental Medicine. 2019

          Adhya et al., Soluble TNF-R1, VEGF and other cytokines as markers of disease activity in systemic lupus erythematosus and lupus nephritis. Lupus. 2019

          Новиков et al., A comparative study of the complete lipopolysaccharide structures and biosynthesis loci of Bordetella avium, B. hinzii, and B. trematum. Biochimie. 2019

          Bougarn et al., A curated transcriptome dataset collection to investigate the blood transcriptional response to viral respiratory tract infection and vaccination.. F1000Research. 2019

    2018

          Boisson‐Dupuis et al., Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant. Science Immunology. 2018

          Rodero et al., Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency. The Journal of Experimental Medicine. 2018

          Béziat et al., A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity. Science Immunology. 2018


    2017

          Claydon et al., Respiratory syncytial virus-neutralizing serum antibody titers in infants following palivizumab prophylaxis with an abbreviated dosing regimen. PLoS ONE. 2017

          Mina et al., Inherited human IRAK-1 deficiency selectively impairs TLR signaling in fibroblasts. Proceedings of the National Academy of Sciences. 2017

    2016

          Rahman et al., A curated transcriptome dataset collection to investigate the functional programming of human hematopoietic cells in early life. F1000Research. 2016

          Lavoie et al., Outcomes of Respiratory Syncytial Virus Immunoprophylaxis in Infants Using an Abbreviated Dosing Regimen of Palivizumab. JAMA Pediatrics. 2016

    2015

          Al-Afif et al., Respiratory syncytial virus infection of primary human mast cells induces the selective production of type I interferons, CXCL10, and CCL4. Journal of Allergy and Clinical Immunology. 2015

    2014

          Marr et al., Assessment of Genetic Associations between Common Single Nucleotide Polymorphisms in RIG-I-Like Receptor and IL-4 Signaling Genes and Severe Respiratory Syncytial Virus Infection in Children: A Candidate Gene Case-Control Study. PLoS ONE. 2014

          McKinnon et al., Combined immunodeficiency associated with homozygous MALT1 mutations. Journal of Allergy and Clinical Immunology. 2014

          Marr et al., Attenuation of Respiratory Syncytial Virus–Induced and RIG-I–Dependent Type I IFN Responses in Human Neonates and Very Young Children. The Journal of Immunology. 2014


    2013

          Marr et al., Pathogen recognition receptor crosstalk in respiratory syncytial virus sensing: a host and cell type perspective. Trends in Microbiology. 2013

          Ali et al., Functional Genetic Variation inNFKBIAand Susceptibility to Childhood Asthma, Bronchiolitis, and Bronchopulmonary Dysplasia. The Journal of Immunology. 2013

          Shah et al., Minor Modifications to the Phosphate Groups and the C3′ Acyl Chain Length of Lipid A in Two Bordetella pertussis Strains, BP338 and 18-323, Independently Affect Toll-like Receptor 4 Protein Activation. Journal of Biological Chemistry. 2013

          You et al., IL-4Rα on CD4+ T cells plays a pathogenic role in respiratory syncytial virus reinfection in mice infected initially as neonates. Journal of Leukocyte Biology. 2013

    2012

          Marr et al., Role of human TLR4 in respiratory syncytial virus-induced NF-κB activation, viral entry and replication. Innate Immunity. 2012

    2011

          Marr et al., Bordetella pertussis Autotransporter Vag8 Binds Human C1 Esterase Inhibitor and Confers Serum Resistance. PLoS ONE. 2011

    2010

          Marr et al., Variability in the Lipooligosaccharide Structure and Endotoxicity amongBordetella pertussisStrains. The Journal of Infectious Diseases. 2010

          Marr et al., Substitution of the Bordetella pertussis Lipid A Phosphate Groups with Glucosamine Is Required for Robust NF-κB Activation and Release of Proinflammatory Cytokines in Cells Expressing Human but Not Murine Toll-Like Receptor 4-MD-2-CD14. Infection and Immunity. 2010

    2008

          Marr et al., Protective activity of the Bordetella pertussis BrkA autotransporter in the murine lung colonization model. Vaccine. 2008

          Marr et al., Glucosamine Found as a Substituent of Both Phosphate Groups in Bordetella Lipid A Backbones: Role of a BvgAS-Activated ArnT Ortholog. Journal of Bacteriology. 2008

    2007

          Marr et al., Bordetella pertussis Binds Human C1 Esterase Inhibitor during the Virulent Phase, to Evade Complement‐Mediated Killing. The Journal of Infectious Diseases. 2007



Last update: 2024-11-18 | Back to Home.