NU 2019-030
INVENTORS John Kessler Sripadh Sharma
ABSTRACT There is no decisive treatment for traumatic brain injury (TBI). After the primary trauma, secondary injury, largely mediated by blood-borne immune cells called monocytes, takes place causing damage to surrounding healthy cells. Furthermore, cellular and whole brain swelling (edema) resulting from this secondary injury causes increased intracranial pressure increasing risk of (and often causing) irreversible brain damage and death. Therapies targeting the various secondary injury mediators have not been successful mainly because of lack of specificity to pro-inflammatory damaging cells. For the first time, Northwestern researchers have characterized the use of a modified FDA-approved material in TBI that is very selective to eliminating a specific subtype of monocytes that cause much of this damage. Using this therapy in multiple TBI models, they have demonstrated initial evidence of preservation of significant amounts of functional brain tissue, a more anti-inflammatory lesion area, and vastly superior behavior recovery in treated animals.
APPLICATIONS
ADVANTAGES
IP STATUS A US application has been filed.
PUBLICATION Sharma S, Ifergan I, Kurz J, Linsenmeier R, Xu D, Cooper D, Miller S and Kessler J (2020) Intravenous Immunomodulatory Nanoparticle Treatment for Traumatic Brain Injury. Annals of Neurology 87: 442-455