Diffuse midline gliomas (DMGs) are inoperable, lethal, high-grade central nervous system cancers primarily affecting children and young adults. We discovered that DMGs, which are characterized by the presence of a specific mutation called H3K27M+, exhibit high levels of a signal called GD2 and that immune cells engineered to recognize this signal called chimeric antigen receptor T cells (GD2-CAR T cells) mediate impressive antitumor effects in numerous patient-derived mouse models of DMG, including spinal cord DMG.

Board of Trustees of the Leland Stanford Junior University
1050 Arastradero Rd.
Palo Alto, CA 94304
United States