Seminar - Dr. Ran Jing
Dr. Ran Jing
MBIM Seminar Series
Starts
Feb 18, 2025 - 12:30 pmAdd to Calendar 2025-02-18 20:30:00 2025-02-18 20:30:00 Seminar - Dr. Ran Jing

Seminar: Harnessing Human Pluripotent Stem Cells for T Cell Development and Cancer Immunotherapy

 

Abstract: Dr. Jing's research leverages human pluripotent stem cells (iPSCs) to study lymphoid development and create stem cell-based immune cell therapies. His previous work demonstrated that EZH1 repression enhances lymphoid potential and generates developmentally mature T cells resembling peripheral blood αβ T cells (Cell Stem Cell, 2022). A small molecule screen further revealed that G9a/GLP inhibition promotes mature T cell generation, with epigenetically reprogrammed iPSC-CAR-T cells displaying enhanced antitumor activity and persistence (Cell Stem Cell, 2024). These findings uncover key regulators of T cell lineage choice and advance the development of iPSC-based adoptive T cell immunotherapies.

LSC 3 (Life Sciences Institute - 2350 Health Sciences Mall) MBIM itsupport@microbiology.ubc.ca America/Vancouver public
Ends
Feb 18, 2025 - 1:30 pm
Location
LSC 3 (Life Sciences Institute - 2350 Health Sciences Mall)
Hosted by
Dr. Marc Horwitz & Dr. Kelly Brown
Presenter title
Instructor, Harvard Medical School and Boston Children's Hospital
Presenter name
Dr. Ran Jing

Seminar: Harnessing Human Pluripotent Stem Cells for T Cell Development and Cancer Immunotherapy

 

Abstract: Dr. Jing's research leverages human pluripotent stem cells (iPSCs) to study lymphoid development and create stem cell-based immune cell therapies. His previous work demonstrated that EZH1 repression enhances lymphoid potential and generates developmentally mature T cells resembling peripheral blood αβ T cells (Cell Stem Cell, 2022). A small molecule screen further revealed that G9a/GLP inhibition promotes mature T cell generation, with epigenetically reprogrammed iPSC-CAR-T cells displaying enhanced antitumor activity and persistence (Cell Stem Cell, 2024). These findings uncover key regulators of T cell lineage choice and advance the development of iPSC-based adoptive T cell immunotherapies.