Project Details
Description
ABSTRACT
Acute Radiation Syndrome (ARS) is a potentially lethal multi-organ failure syndrome resulting from whole or
partial-body exposure to irradiation due to accidents or nuclear terrorism. Currently, four FDA-approved radiation
medical countermeasures (MCMs) are available for treating hematopoietic ARS (H-ARS). However, there is a
significant gap in approved drugs for non-hematopoietic organ systems such as the gastrointestinal (GI). In
collaboration with BioConvergent Health, we are developing a Phase 2 ready, 29-amino acid, fully synthetic,
PEGylated peptide (TPOm), which binds to the thrombopoietin (TPO) receptor, c-Mpl, acting as a TPO mimetic.
TPOm has been shown to induce regeneration of megakaryocytes, platelets, and HSPCs in mice, with or without
exposure to total body irradiation (TBI). Our preliminary studies indicate that TPOm administered 24 hours post-
partial body irradiation (PBI) significantly improves 30-day survival and reduces gut barrier dysfunction, while
promoting intestinal crypt and epithelial regeneration. We have identified several unique pharmacodynamic
effects of TPOm among radiomitigators: stimulating regeneration of c-Mpl-expressing HSPCs, megakaryocytes,
and mesenchymal stromal cells (MSCs) in irradiated BM; inducing proliferation of c-Mpl-expressing
microvascular lung and liver sinusoidal endothelial cells; activating a novel Leptin Receptor (LepR+)/c-Mpl+
MSCs to promote secretion of Wnt ligands and angiogenic growth factors; and promoting mobilization of histidine
decarboxylase (HDC)-expressing granulocytic immature myeloid cells (IMCs) from BM to irradiated organs like
the intestine, stimulating repair and regeneration of tissue stem cells. Based on these features, we hypothesize
that TPOm will mitigate GI-ARS by regenerating HSPCs in irradiated BM, stimulating the secretion of growth
factors, and mobilizing BM-derived IMCs and MSCs into circulation. These cells could home in on irradiated
organs, like the intestine, to promote repair and regeneration of intestinal stem cells (ISCs), thereby mitigating
GI-ARS. Four specific aims are proposed to further develop TPOm as MCM for GI-ARS: 1) Mitigation of GI-ARS
and determining the dose modification factor (DMF) of TPOm; 2) Mechanisms of action (MOA) of TPOm for
radio-mitigation of GI-ARS; 3) Pharmacokinetics/Pharmacodynamics (PK/PD) of TPOm in unirradiated and
irradiated animals; and 4) Comparison of TPOm effectiveness with FDA-approved radiation MCMs and intestinal
mitogens for GI-ARS treatment. This study will illuminate TPOm's mechanisms of action in mitigating GI injury
post-irradiation and provide comprehensive characterization information about TPOm. This could lead to filing
TPOm with the FDA as an investigational new drug (IND) for GI-ARS.
| Status | Finished |
|---|---|
| Effective start/end date | 12/6/24 → 11/30/25 |
Funding
- National Institute of Allergy and Infectious Diseases: $593,823.00
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