Keynote Speakers

Day 1: Opening Keynote, 9:00 – 09:30 am
Élie Haddad

Élie Haddad, MD, PhD, is Professor of Pediatrics and of Microbiology, Infectious Diseases and Immunology at Université de Montréal, Head of the Immunology, Allergy and Rheumatology Division at CHU Sainte-Justine, and the hospital’s Director of Innovative Therapies, responsible for bringing cell and gene therapy products developed in-house to patients.

His laboratory works across the translational chain, from vector engineering to first-in-human administration. He developed efficient lentiviral transduction of NK cells and designed patented synthetic lineage-specific promoters restricting CAR expression to the T- and NK-cell progeny of transduced hematopoietic stem cells, now extended to in vivo CAR delivery and to gene therapy of primary immune deficiency. He was co-first author of the 2026 New England Journal of Medicine report of the first-in-human prime editing trial, in p47-deficient chronic granulomatous disease, whose first patient worldwide was treated at Sainte-Justine. He currently co-leads an ex vivo lentiviral stem cell gene therapy for MPS type IIID, designed and validated entirely within his institution, now at the pre-CTA stage with Health Canada.

He has published 248 peer-reviewed articles cited over 20,000 times, is a multi-PI of the NIH-funded Primary Immune Deficiency Treatment Consortium, and was the first Canadian elected President of the Clinical Immunology Society.

Day 2: Breakfast Keynote, 8:45 – 9:15 am
Steven Gray

Dr. Steven Gray is the Helen J and Robert S Strauss Distinguished Professor in the Department of Pediatrics at the University of Texas Southwestern Medical Center.  Dr. Gray co-directs the UTSW Gene Therapy Program.  He maintains secondary appointments with the Department of Molecular Biology, the Department of Neurology, and the Eugene McDermott Center for Human Growth and Development at UT Southwestern.  Dr. Gray’s core expertise is in AAV gene therapy vector engineering, followed by optimizing approaches to deliver a gene to the nervous system.  His research focus has been heavily focused on developing AAV-based treatments for neurological diseases, several of which have translated into clinical trials. He is inventor on over 25 awarded or pending patents and has authored over 100 publications related to gene therapy