Celine Garcia
Principal Immunologist @ Epitopea
United Kingdom
Cambridge
Biotechnology
Virology, Human Immunology, Immunogenicity testing, High Parameter Flow Cytometry, siRNA, Primary Culture of CD8 T cells and Dendritic cells, Treg Supression assay, T Cell Receptor Signaling, Transduction primary cells with lentivirus, mouse genotyping screening, Bacterial Culture, ELISA, Flow Cytometry, Western Blotting, Virus titration, Culture BSL4, Molecular & Cellular Biology, Fluorescence Microscopy, High parameter Flow Cytometry, Mouse Immunology
Experience

Senior Scientific Associate
Cambridge, England, United Kingdom _ Cancer Research UK
Study the role of Innate Lymphoid Cell type 2 (ILC2) in pancreatic ductal adenocarcinoma (PDAC) The Halim group is interested in understanding the basic immune-regulatory mechanisms in cancer, focusing on a new type of immune-regulatory cell, called the group 2 innate lymphoid cell (ILC2). I was using, and developing, cutting-edge reagents to study how ILC2-driven inflammation is involved in cancer. More specifically, ILC2 are known to directly influence many pro- and anti-cancer immune pathways, making this cell a challenging but potentially important target to investigate. This research will reveal potential new avenues for immunotherapy.

Lab manager
Edinburgh, Scotland, United Kingdom
Regulation of T cell differentiation, activation and homeostasis by the phosphatase Ptpn22. Our overarching question is: how do mutations in genes involved in the activation and regulation of T cell responses contribute to regulation of immune homeostasis and at what point do perturbations in homeostatic mechanisms tip over into autoimmunity? Activation and termination of immune responses are balanced through cross-talk between tyrosine kinases and phosphatases immediately downstream of the T cell receptor (TCR). Changes in expression and point mutations in these influential kinases and phosphatases have been linked to autoimmunity; how do these mutations perturb homeostasis and result in a failure of regulation? At what point do perturbations in the homeostatic balance of the immune system tip into immunopathology and autoimmunity? What are the mechanisms that underlie these processes?
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