Stephanie Dupuis-Boisson

Paris, France

Last Updated: 09/26/2026

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Found 144 publications

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: medRxiv : the preprint server for health sciences

Published: August 01, 2026

Mycobacterial infections and recurrent osteomyelitis in a patient with an autosomal dominant mutation in IFN-gamma receptor 1 with overexpression of the receptor.

Mycobacterial infections and recurrent osteomyelitis in a patient with an autosomal dominant mutation in IFN-gamma receptor 1 with overexpression of the receptor.

Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

Published: May 22, 2026

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans.

Homozygosity for rare or common hypomorphic IL23R variants confers a predisposition to tuberculosis in humans.

Journal: bioRxiv : the preprint server for biology

Published: April 03, 2026

Human LFA-1 governs T cell immune surveillance of the skin.

Human LFA-1 governs T cell immune surveillance of the skin.

Journal: Science immunology

Published: February 27, 2026

Chronic granulomatous disease: Clinical, microbial, and genetic findings in 39 Colombian patients.

Chronic granulomatous disease: Clinical, microbial, and genetic findings in 39 Colombian patients.

Journal: Journal of human immunity

Published: December 13, 2025

Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.

Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis.

Journal: The Journal of experimental medicine

Published: October 27, 2025

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Human-inherited RORγT deficiency encompasses genetic heterogeneity, T cell deficiency, and clinical homogeneity.

Journal: The Journal of experimental medicine

Published: October 01, 2025

Mepolizumab treatment in a child with inherited TYK2 deficiency.

Mepolizumab treatment in a child with inherited TYK2 deficiency.

Journal: Journal of human immunity

Published: September 15, 2025

Human iPSC derived alveolar macrophages reveal macrophage subtype specific functions of itaconate in M. tuberculosis host defense.

Human iPSC derived alveolar macrophages reveal macrophage subtype specific functions of itaconate in M. tuberculosis host defense.

Journal: bioRxiv : the preprint server for biology

Published: August 08, 2025

Human iPSC-derived alveolar macrophages reveal macrophage subtype functions of itaconate in M. tuberculosis defense.

Human iPSC-derived alveolar macrophages reveal macrophage subtype functions of itaconate in M. tuberculosis defense.

Journal: JCI insight

Published: July 23, 2025

Human LY9 governs CD4+ T cell IFN-γ immunity to Mycobacterium tuberculosis.

Human LY9 governs CD4+ T cell IFN-γ immunity to Mycobacterium tuberculosis.

Journal: Science immunology

Published: May 30, 2025

ARAP2 regulates responses to interferon-gamma by restricting SOCS1.

ARAP2 regulates responses to interferon-gamma by restricting SOCS1.

Journal: Cell reports

Published: March 12, 2025

Showing 1-12 of 144

Last Updated: 09/26/2026