Dr David Zahra
Dr David Zahra obtained his Honours degree in Science from the University of Sydney in 1991 where he majored in Chemistry and Genetics. He completed his PhD in 1995 under the supervision of Roger Reddel at the Children’s Medical Research Institute where he worked on viral proteins that facilitate the immortalisation of human cells.
In 1996 he took up a research scientist position at the CRC for Biopharmaceuticals where he developed an in vitro antibody library maturation process to improve the ability to isolate antibodies against a number of targets. In 1999 he moved to the University of New South Wales and undertook studies into the causes of rheumatoid arthritis and developed a tissue bank from arthritic patients in conjunction with St Vincent’s Hospital at Darlinghurst.
In 2002, he was recruited to the Garvan Institute of Medical Research’s Immunology program. David developed a number of antibodies for the treatment of inflammatory disease. Antibodies were isolated from mice against difficult targets and these antibodies were shown to be effective in the treatment of inflammatory disease. Two key antibodies were humanised and developed for pre-clinical analysis prior to being licenced to major pharmaceutical companies for human pre-clinical and clinical trials.
In 2013, David was appointed as a Group Leader of the Genomic Engineering Group in the Institute’s Immunology Division.
Selected publications
See all publications- 2023The Journal of Experimental Medicine10.1084/jem.20221020
Human PIK3R1 mutations disrupt lymphocyte differentiation to cause activated PI3Kδ syndrome 2.
- 2022Nature10.1038/s41586-022-05054-9
The retroelement Lx9 puts a brake on the immune response to virus infection.
- 2021Immunity10.1016/j.immuni.2021.03.013
Positive selection of IgG over IgM B cells in the germinal center reaction.
- 2019Nature Immunology10.1038/s41590-019-0492-0
Denisovan, modern human and mouse TNFAIP3 alleles tune A20 phosphorylation and immunity.
- 2019The Journal of Allergy and Clinical Immunology10.1016/j.jaci.2019.02.010
B cell-intrinsic requirement for STK4 in humoral immunity in mice and human subjects.