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Development of passive immunity against SARS-CoV-2 for management of immunodeficient patients—a perspective

Journal of allergy and clinical immunology, 2020-07, Vol.146 (1), p.58-60

2020

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Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria

Cell, 2020-12, Vol.183 (7), p.1826-1847.e31

2020

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Genetic and immunologic evaluation of children with inborn errors of immunity and severe or critical COVID-19

Journal of allergy and clinical immunology, 2022-11, Vol.150 (5), p.1059-1073

2022

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Defects in plasma cell differentiation are associated with primary immunodeficiency in human subjects

Journal of allergy and clinical immunology, 2018-04, Vol.141 (4), p.1217-1219

2018

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SARS-CoV-2–specific B- and T-cell immunity in a population-based study of young Swedish adults

Journal of allergy and clinical immunology, 2022-01, Vol.149 (1), p.65-75.e8

2022

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Causative mechanisms and clinical impact of immunoglobulin deficiencies in ataxia telangiectasia

Journal of allergy and clinical immunology, 2024-05, Vol.153 (5), p.1392-1405

2024

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Mesoscale DNA feature in antibody-coding sequence facilitates somatic hypermutation

Cell, 2023-05, Vol.186 (10), p.2193-2207.e19

2023

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XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency

Journal of allergy and clinical immunology, 2015-10, Vol.136 (4), p.1007-1017

2015

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New facets of antibody deficiencies

Current opinion in immunology, 2013-10, Vol.25 (5), p.629-638

2013

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APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humans

Journal of allergy and clinical immunology, 2020-11, Vol.146 (5), p.1109-1120.e4

2020

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A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency

Journal of allergy and clinical immunology, 2014-12, Vol.134 (6), p.1375-1380

2014

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RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency

Journal of allergy and clinical immunology, 2015-05, Vol.135 (5), p.1380-1384.e5

2015

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Gut Microbiota Perturbation in IgA Deficiency Is Influenced by IgA-Autoantibody Status

Gastroenterology (New York, N.Y. 1943), 2021-06, Vol.160 (7), p.2423-2434.e5

2021

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Selective IgA deficiency in early life: Association to infections and allergic diseases during childhood

Clinical immunology (Orlando, Fla.), 2009-10, Vol.133 (1), p.78-85

2009

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Synergistic antitumor effect of histone deacetylase inhibitor and Doxorubicin in peripheral T-cell lymphoma

Leukemia research, 2017-05, Vol.56, p.29-35

2017

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Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles

Journal of allergy and clinical immunology, 2013-05, Vol.131 (5), p.1437-1440.e5

2013

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Study of an extended family with CTLA-4 deficiency suggests a CD28/CTLA-4 independent mechanism responsible for differences in disease manifestations and severity

Clinical immunology (Orlando, Fla.), 2018-03, Vol.188, p.94-102

2018

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Differential mechanisms for T lymphocyte recruitment in normal and neoplastic human gastric mucosa

Clinical Immunology, 2006, Vol.118 (1), p.24-34

2006

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Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation

Stem cell research, 2019-12, Vol.41, p.101612-101612, Article 101612

2019

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Class Switch Recombination: A Comparison Between Mouse and Human

Advances in Immunology, 2007, Vol.93, p.1-61

2007

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Reduced immunoglobulin gene diversity in patients with Cornelia de Lange syndrome

Journal of allergy and clinical immunology, 2018-01, Vol.141 (1), p.408-411.e8

2018

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Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency

Stem cell research, 2019-12, Vol.41, p.101613-101613, Article 101613

2019

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Development of passive immunity against SARS-CoV-2 for management of immunodeficient patients—a perspective

Deleterious Mutations in LRBA Are Associated with a Syndrome of Immune Deficiency and Autoimmunity

B Cell Super-Enhancers and Regulatory Clusters Recruit AID Tumorigenic Activity

Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria

Genetic and immunologic evaluation of children with inborn errors of immunity and severe or critical COVID-19

Defects in plasma cell differentiation are associated with primary immunodeficiency in human subjects

SARS-CoV-2–specific B- and T-cell immunity in a population-based study of young Swedish adults

Causative mechanisms and clinical impact of immunoglobulin deficiencies in ataxia telangiectasia

Mesoscale DNA feature in antibody-coding sequence facilitates somatic hypermutation

XRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency

New facets of antibody deficiencies

APRIL-dependent lifelong plasmacyte maintenance and immunoglobulin production in humans

A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency

Quantification of κ-deleting recombination excision circles in Guthrie cards for the identification of early B-cell maturation defects

RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency

Gut Microbiota Perturbation in IgA Deficiency Is Influenced by IgA-Autoantibody Status

Selective IgA deficiency in early life: Association to infections and allergic diseases during childhood

Synergistic antitumor effect of histone deacetylase inhibitor and Doxorubicin in peripheral T-cell lymphoma

Common variable immunodeficiency classification by quantifying T-cell receptor and immunoglobulin κ-deleting recombination excision circles

Study of an extended family with CTLA-4 deficiency suggests a CD28/CTLA-4 independent mechanism responsible for differences in disease manifestations and severity

Differential mechanisms for T lymphocyte recruitment in normal and neoplastic human gastric mucosa

Generation of a human induced pluripotent stem cell line (PHAi003) from a primary immunodeficient patient with CD70 mutation

Class Switch Recombination: A Comparison Between Mouse and Human

Reduced immunoglobulin gene diversity in patients with Cornelia de Lange syndrome

Generation of human induced pluripotent stem cell lines from patients with selective IgA deficiency

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