Publications by authors named "Yoann Seeleuthner"

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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jeremy Manry, Yoann Seeleuthner, Yu Zhang, Alexandre Bolze, Matthieu Chaldebas, Baptiste Milisavljevic

Genome Med· April 2023

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A promoter variant underlying Wiskott-Aldrich syndrome in two kindreds.
Pauline Ober, Christelle Lenoir, Arnaud Maillard, Marie-Gabrielle Vigue, Marjolaine Willems, Yoann Seeleuthner

J Hum Immun· January 2026

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A human YEATS4 variant confers resistance to TST and IGRA conversion despite Mycobacterium tuberculosis exposure.
Clément Conil, Jonathan Bohlen, Elouise E Kroon, Marc A Jean-Juste, Jérémy Manry, Yoann Seeleuthner

Genome Med· October 2025

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Intronic branchpoint-to-acceptor variants underlying inborn errors of immunity.
Najiba Alioua, Nathalie Lambert, Mathilde Puel, Sylvain Hanein, Paul Bastard, Yoann Seeleuthner

J Hum Immun· September 2025

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Human LY9 governs CD4 T cell IFN-γ immunity to .
Masato Ogishi, Julia Puchan, Rui Yang, Andrés Augusto Arias, Ji Eun Han, Yoann Seeleuthner

Sci Immunol· May 2025

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Heterozygous BTNL8 variants in individuals with multisystem inflammatory syndrome in children (MIS-C).
Evangelos Bellos, Dilys Santillo, Pierre Vantourout, Heather R Jackson, Amedine Duret, Yoann Seeleuthner

J Exp Med· December 2024

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Case report: A novel homozygous variant in a patient with severe combined immunodeficiency and persistent COVID-19.
Renan Cesar Sbruzzi, Mayara Jorgens Prado, Bibiana Fam, Helena Ashton Prolla, Alessandra Hellwig, Yoann Seeleuthner

Front Immunol· November 2024

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IL-7-dependent and -independent lineages of IL-7R-dependent human T cells.
Carlos A Arango-Franco, Masato Ogishi, Susanne Unger, Ottavia M Delmonte, Julio César Orrego, Yoann Seeleuthner

J Clin Invest· October 2024

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Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activation.
Jonathan Bohlen, Ivan Bagarić, Taja Vatovec, Masato Ogishi, Syed F Ahmed, Yoann Seeleuthner

J Clin Invest· October 2024

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SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency.
Yi-Hao Chan, Vanja Lundberg, Jérémie Le Pen, Jiayi Yuan, Danyel Lee, Yoann Seeleuthner

J Exp Med· September 2024

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Tuberculosis in otherwise healthy adults with inherited TNF deficiency.
Andrés A Arias, Anna-Lena Neehus, Masato Ogishi, Vincent Meynier, Adam Krebs, Yoann Seeleuthner

Nature· September 2024

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Human TMEFF1 is a restriction factor for herpes simplex virus in the brain.
Yi-Hao Chan, Zhiyong Liu, Paul Bastard, Noopur Khobrekar, Kennen M Hutchison, Yoann Seeleuthner

Nature· August 2024

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Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.
Matthew B Johnson, Masato Ogishi, Clara Domingo-Vila, Elisa De Franco, Matthew N Wakeling, Yoann Seeleuthner

J Exp Med· June 2024

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Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Anna-Lena Neehus, Brenna Carey, Marija Landekic, Patricia Panikulam, Gail Deutsch, Yoann Seeleuthner

Cell· June 2024

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Helper T cell immunity in humans with inherited CD4 deficiency.
Antoine Guérin, Marcela Moncada-Vélez, Katherine Jackson, Masato Ogishi, Jérémie Rosain, Yoann Seeleuthner

J Exp Med· May 2024

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FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice.
Mana Momenilandi, Romain Lévy, Steicy Sobrino, Jingwei Li, Chantal Lagresle-Peyrou, Yoann Seeleuthner

Cell· May 2024

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The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants.
Marie Materna, Ottavia M Delmonte, Marita Bosticardo, Mana Momenilandi, Peyton E Conrey, Yoann Seeleuthner

Science· March 2024

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Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.
Jessica N Peel, Rui Yang, Tom Le Voyer, Adrian Gervais, Jérémie Rosain, Yoann Seeleuthner

J Clin Invest· March 2024

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Human inherited CCR2 deficiency underlies progressive polycystic lung disease.
Anna-Lena Neehus, Brenna Carey, Marija Landekic, Patricia Panikulam, Gail Deutsch, Yoann Seeleuthner

Cell· January 2024

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Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19.
Daniela Matuozzo, Estelle Talouarn, Astrid Marchal, Peng Zhang, Jeremy Manry, Yoann Seeleuthner

Genome Med· January 2024

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Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.
Mohadese Sadat Mousavi Khorshidi, Yoann Seeleuthner, Zahra Chavoshzadeh, Maryam Behfar, Amir Ali Hamidieh

J Clin Immunol· November 2023

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Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria.
Jonathan Bohlen, Qinhua Zhou, Quentin Philippot, Masato Ogishi, Darawan Rinchai, Yoann Seeleuthner

Cell· November 2023

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Encephalitis and poor neuronal death-mediated control of herpes simplex virus in human inherited RIPK3 deficiency.
Zhiyong Liu, Eduardo J Garcia Reino, Oliver Harschnitz, Hongyan Guo, Yi-Hao Chan, Yoann Seeleuthner

Sci Immunol· April 2023

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Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria.
Jérémie Rosain, Anna-Lena Neehus, Jérémy Manry, Rui Yang, Jérémie Le Pen, Yoann Seeleuthner

Cell· February 2023

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Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria.
Quentin Philippot, Masato Ogishi, Jonathan Bohlen, Julia Puchan, Andrés Augusto Arias, Yoann Seeleuthner

Sci Immunol· February 2023

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