# Targeting cDC1 with CAR T cells to investigate their role and potential as a therapeutic target in Type 1 diabetes

> **NIH NIH F31** · WASHINGTON UNIVERSITY · 2024 · $34,623

## Abstract

PROJECT SUMMARY
Type 1 diabetes (T1D) is the second most common disease of childhood which results in substantial morbidity
and mortality. This autoimmune disease is characterized by the infiltration of CD4 and CD8 T cells into the islets
of Langerhans in the pancreas, where they ultimately deplete insulin-secreting  cells. Recent studies have
shown that conventional type 1 dendritic cells (cDC1) are required for the development of Type 1 diabetes in the
murine NOD model, which has many parallels to human disease. cDC1 are unique in their ability to efficiently
cross-present  cell antigens to and prime autoreactive CD8 T cells. Furthermore, cDC1 are potent producers of
IL-12 and may facilitate Th1 differentiation of CD4 T cells. A therapy that specifically eliminates cDC1 may
therefore be expected to prevent the development of T1D by blocking autoreactive CD4 Th1 development as
well as the presentation of self-antigens to autoreactive CD8 T cells. Our preliminary data show that a chimeric
antigen receptor (CAR) T cell targeting XCR1, a chemokine receptor expressed by cDC1, is successful in
depleting cDC1 in the spleen and pancreatic lymph node of NOD mice. Furthermore, cDC1 depletion by this
CAR T cell also successfully inhibited the proliferation of a cDC1 dependent, self-reactive CD4 T cell in vivo.
Thus, the central premise of this proposal is that XCL1 CAR T cells may be useful for the prevention of T1D.
To address this, we will assess the ability of this CAR to prevent diabetes in NOD mice. Experiments proposed
in Aim 1 will validate the specificity of the CAR for cDC1s and address the durability of cDC1 depletion in vivo.
Aim 2 will assess the functional effects of cDC1 depletion by CAR T cells on autoimmune diabetes by assessing
CD4 and CD8 T cell numbers and phenotypes within the islets as well as the rate of spontaneous diabetes
incidence in NOD mice. Collectively, these studies may lead to the development of a novel preventative treatment
for human Type 1 diabetes and establish a paradigm for CAR T cell mediated immunomodulation via selective
targeting of DC subsets.

## Key facts

- **NIH application ID:** 10996718
- **Project number:** 1F31DK139666-01A1
- **Recipient organization:** WASHINGTON UNIVERSITY
- **Principal Investigator:** Omar Abousaway
- **Activity code:** F31 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $34,623
- **Award type:** 1
- **Project period:** 2024-09-01 → 2027-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10996718

## Citation

> US National Institutes of Health, RePORTER application 10996718, Targeting cDC1 with CAR T cells to investigate their role and potential as a therapeutic target in Type 1 diabetes (1F31DK139666-01A1). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10996718. Licensed CC0.

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