
Jean Gariépy
Research Assistant:
Biotherapies including immunotherapies have had a dramatic impact in terms of patient survival and enhanced quality of life in the areas of inflammatory diseases and cancer. Dr. Gariépy’s laboratory is interested in the design and engineering of protein- and oligonucleotide-based therapeutics aimed at modulating immune responses to either selectively dampen them (anti-inflammatory agents) or release such responses (to target and kill cancer cells). His lab creates and tests such agents by combining synthetic, combinatorial and genetic approaches with cellular assays and animal studies. The team also designs probes and devises new methods that can serve as new diagnostic or discovery tools. Additionally, they collaborate with clinicians and scientists at Sunnybrook Research Institute and elsewhere in the world as what they do is applicable to any disease.
Education:
- B.Sc., 1978, biochemistry specialization, Concordia University, Canada
- PhD, 1983, biochemistry, University of Alberta, Canada
- Postdoctoral fellow, 1986, medical microbiology, Stanford University, U.S.
Appointments and Affiliations:
- Senior scientist, Physical Sciences, Odette Cancer Research Program, Sunnybrook Research Institute
- SRI Research Chair in Biomolecular Engineering
- Professor, department of medical biophysics, University of Toronto
- Professor (cross-appointment), department of pharmaceutical sciences, University of Toronto
Research Foci
- Adoptive cell therapies
- Anti-cancer agents
- Anti-inflammatory agents
- Antibodies
- Aptamers
- Aptamers as therapeutics
- Bispecifics
- Cancer vaccines
- Designing novel diagnostic approaches
- Immune checkpoint inhibitors for cancer therapy
- Immune checkpoint therapies
- Immunotherapy
- Protein therapeutics
- Targeted therapies
- Translational research
Publications
Affiliated Labs & Programs
Selected Publications
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Prodeus A, Abdul-Wahid A, Sparkes A, Fischer NW, Cydzik M, Chiang N, Alwash M, Ferzoco A, Vacaresse N, Julius M, Gorczysnki RM, and Gariépy J. VISTA.COMP: an engineered checkpoint receptor agonist that potently suppresses T-cell mediated immune responses. JCI Insight 2017 (in press).
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Fischer NW, Prodeus A, Malkin D, Gariépy J. p53 oligomerization status modulates cell fate decisions between growth, arrest and apoptosis. Cell Cycle. 2016 Dec;15(23):3210–3219.
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Abdul-Wahid A, Cydzik M, Prodeus A, Alwash M, Stanojcic M, Thompson M, Huang EH, Shively JE, Gray-Owen SD, Gariépy J.Induction of antigen-specific TH 9 immunity accompanied by mast cell activation blocks tumor cell engraftment. Int J Cancer. 2016 Aug 15;139(4):841–53
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Cydzik M, Abdul-Wahid A, Park S, Bourdeau A, Bowden K, Prodeus A, Kollara A, Brown TJ, Ringuette MJ, Gariépy J. Slow binding kinetics of secreted protein, acidic, rich in cysteine-VEGF interaction limit VEGF activation of VEGF receptor 2 and attenuate angiogenesis. FASEB J. 2015 Aug;29(8):3493–505.
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Prodeus A, Abdul-Wahid A, Fischer NW, Huang EH, Cydzik M, Gariépy J. Targeting the PD-1/PD-L1 Immune Evasion Axis With DNA Aptamers as a Novel Therapeutic Strategy for the Treatment of Disseminated Cancers. Mol Ther Nucleic Acids. 2015 Apr 28;4:e237.
In the News
- Mutations in tumour-halting gene may be useful markers for prognosis: More active forms of gene linked to longer survival of people with cancer
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Researchers discover that mutations in tumour-halting gene may be useful markers for prognosis: more active p53 gene linked to longer survival in certain cancer patients
August 17, 2018
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Resounding approval: Sunnybrook Research Institute's success rate in CIHR competition soars past national average
January 25, 2018