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| Funder | NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE |
|---|---|
| Recipient Organization | University of Michigan At Ann Arbor |
| Country | United States |
| Start Date | Jul 15, 2021 |
| End Date | Jun 30, 2026 |
| Duration | 1,811 days |
| Number of Grantees | 2 |
| Roles | Co-Investigator; Principal Investigator |
| Data Source | NIH (US) |
| Grant ID | 10622660 |
Gliomas are highly aggressive brain tumors and complete tumor resection is not achievable as residual tumor cells routinely infiltrate the surrounding functional brain tissue and are protected by the blood brain barrier (BBB). The BBB presents a significant obstacle for effective delivery of therapeutic agents to the central nervous system.
The BBB forms a highly selective semipermeable border that prevents solutes in the circulating blood from crossing into the intracranial environment. Thus, there is an urgent need for new approaches for drug delivery through the BBB to gliomas. To address these major unmet medical needs, here we propose to develop new
nanoparticles for delivering STING agonist to gliomas. We will develop nanoparticles that can be tuned with different targeting moieties and effectively delivered to gliomas; elicit anti-tumor immune response by converting the “cold” glioma tumors to “hot” tumors; eradicate established gliomas; and generate sustained anti-gliomas
immunity. This Supplement application focuses on applying the knowledge gained from the parent R01 grant to target STING agonists to gliomas and achieve anti-tumor immunity against gliomas. Therefore, this represents a new and complementary research component that directly relates to original goals of the grant and broadens
its translational potential and application.
University of Michigan At Ann Arbor
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