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Sven Kracker is a CNRS research director in the Human Lymphohematopoisis laboratory at Imagine institute. He obtained his PhD at the Humboldt University in Berlin, Germany and pursued his research at Harvard Medical School in the laboratory of Klaus Rajewsky and afterwards at Necker-Enfants Malades hospital under the supervision of Anne Durandy. In his projects, he investigates the molecular basis for primary antibody deficiencies due to phenotypic, functional and genetic analysis. The final aim of his research is to identify novel therapeutic targets for treatments. He participated in the description of several causes for primary antibody deficiencies among them the activated PI3Kd-signaling caused by mutation in PIK3CD and PIK3R1. His work is supported by French national grants and charitable grants foundations.
Resources & publications
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Journal (source)J Allergy Clin Immunol. 2018
Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndr...
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Journal (source)Science Immunology
A multimorphic mutation in IRF4 causes human autosomal dominant combined immu...
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Journal (source)J Allergy Clin Immunol
Improving the diagnostic efficiency of primary immunodeficiencies with target...
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Journal (source)Front Immunol
Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-K...
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Journal (source)J Pediatr
From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine D...
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Journal (source)Blood
Topoisomerase 2β mutation impairs early B-cell development.
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Journal (source)J Allergy Clin Immunol
Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndr...
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Journal (source)Front Immunol
Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-K...
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Journal (source)J Allergy Clin Immunol
Improving the diagnostic efficiency of primary immunodeficiencies with target...
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Journal (source)J. Clin. Invest.
Loss of ARHGEF1 causes a human primary antibody deficiency.
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Journal (source)J Immunol
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension ...
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Journal (source)J. Exp. Med.
Concomitant PIK3CD and TNFRSF9 deficiencies cause chronic active Epstein-Barr...
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Journal (source)J. Pediatr.
From Dysgammaglobulinemia to Autosomal-Dominant Activation-Induced Cytidine D...
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Journal (source)J. Allergy Clin. Immunol.
X-linked primary immunodeficiency associated with hemizygous mutations in the...
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Journal (source)J. Clin. Invest.
A human immunodeficiency caused by mutations in the PIK3R1 gene.
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Journal (source)J. Allergy Clin. Immunol. 2017
Clinical and immunologic phenotype associated with activated phosphoinositide...
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Journal (source)Haematologica
Mutations in the adaptor-binding domain and associated linker region of p110δ...