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Active NON-SBIR/STTR RPGS NIH (US)

MAIT cells as a therapeutic approach for gastrointestinal cancers

$3.84M USD

Funder NATIONAL CANCER INSTITUTE
Recipient Organization University of Utah
Country United States
Start Date May 03, 2024
End Date Apr 30, 2026
Duration 727 days
Number of Grantees 2
Roles Co-Investigator; Principal Investigator
Data Source NIH (US)
Grant ID 10865685
Grant Description

Project Summary Colon cancer remains the 3rd most commonly diagnosed cancer and the 3rd highest cancer related mortalities in both men and women. Tumors are often resected, but there are less treatment options available for those diagnosed in later stages. Immunotherapy has had mixed results in colon cancer and thus, new therapeutic

strategies are needed to improve outcome for particularly late stage patients. We have been examining mucosal associated invariant T (MAIT) cells as a subset of T cells that display innate effector qualities, with the potential to be harnessed as HLA-independent immunotherapeutic agents. We have found that MAIT cells have the potential to decrease tumor growth and have identified a potential

mechanism by which MAIT cells enhance innate immune cell responses in order to promote anti-tumor immunity. Based on our novel preliminary data, we propose to test the hypothesis that MAIT cells have the capacity for anti-tumor effects, through both direct cytotoxicity in a T cell receptor-dependent manner, and

indirect mechanisms through the recruitment of innate immune cells. To test this hypothesis, we propose carefully designed experiments to examine the potential of MAIT cells for therapeutic potential using primary human cells in organoid models and mouse tumors in therapeutic approaches in preclinical models.

Furthermore, we will test this therapeutic approach in combination with checkpoint therapy to enhance anti- tumor cytotoxic activity. Data collected for this project could lead to a novel immunotherapy approach for gastrointestinal cancers.

All Grantees

University of Utah

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