Simon J. Pelham

St. Vincent's Clinical School
Sydney, NSW 2052, Australia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 24 publications

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

Signal Transducer and Activator of Transcription 3 (STAT3) Variant p.K709N Causes Hyper-IgE Syndrome Likely by Impaired STAT3-Dimer Formation.

Signal Transducer and Activator of Transcription 3 (STAT3) Variant p.K709N Causes Hyper-IgE Syndrome Likely by Impaired STAT3-Dimer Formation.

Journal: European journal of immunology

Published: June 06, 2024

Tuberculosis in otherwise healthy adults with inherited TNF deficiency.

Tuberculosis in otherwise healthy adults with inherited TNF deficiency.

Journal: Nature

Published: January 07, 2024

Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling.

Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling.

Journal: Immunity

Published: September 09, 2023

Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria.

Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria.

Journal: Science immunology

Published: February 10, 2023

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis.

Journal: The Journal of experimental medicine

Published: March 17, 2022

STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis.

STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis.

Journal: The Journal of allergy and clinical immunology

Published: December 15, 2021

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.

Journal: Science immunology

Published: July 13, 2021

Biallelic TRAF3IP2 variants causing chronic mucocutaneous candidiasis in a child harboring a STAT1 variant.

Biallelic TRAF3IP2 variants causing chronic mucocutaneous candidiasis in a child harboring a STAT1 variant.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: May 17, 2021

Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.

Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents.

Journal: The Journal of clinical investigation

Published: April 01, 2021

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.

Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.

Journal: The Journal of experimental medicine

Published: March 09, 2021

A Novel TRAF3IP2 Mutation Causing Chronic Mucocutaneous Candidiasis.

A Novel TRAF3IP2 Mutation Causing Chronic Mucocutaneous Candidiasis.

Journal: Journal of clinical immunology

Published: January 27, 2021

Showing 1-12 of 24

Last Updated: 09/26/2026