# Pre-Exposure Prophylaxis with Vasculotide Enhances Survival and Alleviates Hematopoietic and Gastrointestinal Injury Following Lethal Total Body Irradiation

**Authors:** Li Wang, Bin Lin, Min Zhai, Lisa Hull, Asher Rothstein, Katherine S. Cleveland, Hengying Ellery, Wanchang Cui, Mang Xiao, Juliann G. Kiang

PMC · DOI: 10.3390/ijms27042001 · International Journal of Molecular Sciences · 2026-02-19

## TL;DR

A new drug called Vasculotide, given before radiation exposure, improves survival and reduces injury in mice after lethal radiation.

## Contribution

Vasculotide is introduced as a novel pre-exposure prophylaxis targeting vascular protection against radiation injury.

## Key findings

- Vasculotide increased 30-day survival in mice by 30% at 20 μg/kg dose.
- Vasculotide reduced vascular injury and protected bone marrow and GI tract.
- The drug shows promise as a medical countermeasure for Acute Radiation Syndrome.

## Abstract

No US Food and Drug Administration (FDA)-approved prophylaxis is currently available for Acute Radiation Syndrome (ARS), which remains a significant threat to military and civilian populations. In this study, we investigated Vasculotide (VT), a Tie2 receptor agonist mimic, as a novel pre-exposure prophylaxis designed to stabilize the vascular endothelium, one of primary targets of radiation-induced damage. To evaluate its efficacy, female B6D2F1/J mice were exposed to 9.5 Gy total body irradiation (TBI), with VT administered subcutaneously at 12 and 2 h prior to exposure. Assessments included 30-day survival, biomarkers of vascular injury, proinflammatory cytokine/chemokine profiling, and evaluation of hematopoietic (H) and gastrointestinal (GI) recovery. Our findings demonstrate that VT significantly increased 30-day survival in a dose-dependent manner, achieving a 30% survival advantage at the 20 μg/kg dose. Furthermore, VT provided robust protection against radiation-induced vascular activation and injury, effectively alleviating damage to the bone marrow (BM) and GI tract. Taken together, these results identify VT as a promising prophylactic countermeasure for ARS. By targeting the Tie2 pathway to preserve vascular integrity, VT addresses a critical gap in medical countermeasures, offering a viable strategy to enhance survival and accelerate multi-organ recovery in radiological mass-casualty scenarios.

## Linked entities

- **Proteins:** TEK (TEK receptor tyrosine kinase)
- **Diseases:** Acute Radiation Syndrome (MONDO:0033938)

## Full-text entities

- **Genes:** Icam1 (intercellular adhesion molecule 1) [NCBI Gene 15894] {aka CD54, Icam-1, Ly-47, MALA-2}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 22339] {aka L-VEGF, Vegf, Vpf}, Il4 (interleukin 4) [NCBI Gene 16189] {aka BSF-1, Il-4}, stm (stumpy) [NCBI Gene 20882], Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Il13 (interleukin 13) [NCBI Gene 16163] {aka Il-13}, Csf2 (colony stimulating factor 2 (granulocyte-macrophage)) [NCBI Gene 12981] {aka CSF, Csfgm, GMCSF, Gm-CSf, MGI-IGM}, Cma1 (chymase 1, mast cell) [NCBI Gene 17228] {aka MMCP-5, Mcp-5, Mcp5, Mcpt5}, Il12b (interleukin 12b) [NCBI Gene 16160] {aka Il-12b, Il-12p40, Il12p40, p40}, Csf1 (colony stimulating factor 1 (macrophage)) [NCBI Gene 12977] {aka BAP025, Csfm, MCSF, Mhdabap25, PG-M-CSF, op}, Lif (leukemia inhibitory factor) [NCBI Gene 16878], Ccl3 (C-C motif chemokine ligand 3) [NCBI Gene 20302] {aka G0S19-1, LD78alpha, MIP-1alpha, MIP1-(a), MIP1-alpha, Mip1a}, Ccl19 (C-C motif chemokine ligand 19) [NCBI Gene 24047] {aka CKb11, ELC, Gm2023, MIP3B, Scya19, exodus-3}, Cxcl2 (C-X-C motif chemokine ligand 2) [NCBI Gene 20310] {aka CINC-2a, GROb, Gro2, MIP-2, MIP-2a, Mgsa-b}, Csf3 (colony stimulating factor 3 (granulocyte)) [NCBI Gene 12985] {aka Csfg, G-CSF, MGI-IG}, Epo (erythropoietin) [NCBI Gene 13856], Il17a (interleukin 17A) [NCBI Gene 16171] {aka Ctla-8, Ctla8, IL-17, IL-17A, Il17}, Ccl22 (C-C motif chemokine ligand 22) [NCBI Gene 20299] {aka ABCD-1, DCBCK, MDC, Scya22}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, Il5 (interleukin 5) [NCBI Gene 16191] {aka Il-5}, Il1a (interleukin 1 alpha) [NCBI Gene 16175] {aka Il-1a}, Ccl5 (C-C motif chemokine ligand 5) [NCBI Gene 20304] {aka MuRantes, RANTES, SISd, Scya5, TCP228}, Il16 (interleukin 16) [NCBI Gene 16170] {aka mKIAA4048}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Ccl4 (C-C motif chemokine ligand 4) [NCBI Gene 20303] {aka AT744.1, Act-2, MIP-1B, Mip1b, Scya4}, Il15 (interleukin 15) [NCBI Gene 16168] {aka IL-15}, Ccl11 (C-C motif chemokine ligand 11) [NCBI Gene 20292] {aka Scya11, eotaxin}, Cxcl10 (C-X-C motif chemokine ligand 10) [NCBI Gene 15945] {aka C7, CRG-2, INP10, IP-10, IP10, Ifi10}, Serpine1 (serine (or cysteine) peptidase inhibitor, clade E, member 1) [NCBI Gene 18787] {aka PAI-1, PAI1, Planh1}, Il11 (interleukin 11) [NCBI Gene 16156] {aka IL-11}, Cxcl5 (C-X-C motif chemokine ligand 5) [NCBI Gene 20311] {aka AMCF-II, Cxcl6, ENA-78, GCP-2, LIX, Scyb5}, Mcpt1 (mast cell protease 1) [NCBI Gene 17224] {aka Mcp-1}, Cxcl9 (C-X-C motif chemokine ligand 9) [NCBI Gene 17329] {aka CMK, Mig, MuMIG, Scyb9, crg-10}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il7 (interleukin 7) [NCBI Gene 16196] {aka A630026I06Rik, Il-7, hlb368}, Il2 (interleukin 2) [NCBI Gene 16183] {aka Il-2}, Cx3cl1 (C-X3-C motif chemokine ligand 1) [NCBI Gene 20312] {aka ABCD-3, CX3C, Cxc3, D8Bwg0439e, FK, Scyd1}, Ccl17 (C-C motif chemokine ligand 17) [NCBI Gene 20295] {aka Abcd-2, Scya17, Scya17l, Tarc}, Mmp9 (matrix metallopeptidase 9) [NCBI Gene 17395] {aka B/MMP9, Clg4b, Gel B, MMP-9, pro-MMP-9}, Ccl20 (C-C motif chemokine ligand 20) [NCBI Gene 20297] {aka CKb4, LARC, MIP-3A, MIP-3[a], MIP3A, ST38}, Il3 (interleukin 3) [NCBI Gene 16187] {aka BPA, Csfmu, HCGF, Il-3, MCGF, PSF}, Ang (angiogenin, ribonuclease, RNase A family, 5) [NCBI Gene 11727] {aka Ang1, Rnase5, Rnase5a}, Tek (TEK receptor tyrosine kinase) [NCBI Gene 21687] {aka Cd202b, Hyk, STK1, Tie-2, Tie2}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Ifnb1 (interferon beta 1, fibroblast) [NCBI Gene 15977] {aka IFN-beta, IFNB, If1da1, Ifb}, Akt1 (Akt serine/threonine kinase 1) [NCBI Gene 11651] {aka Akt, LTR-akt, PKB, PKB/Akt, PKBalpha, Rac}, Il20 (interleukin 20) [NCBI Gene 58181] {aka If2d, Zcyto10}, Il9 (interleukin 9) [NCBI Gene 16198] {aka Il-9, P40}
- **Diseases:** vascular disorders (MESH:D002561), Vascular Injury (MESH:D057772), lethargy (MESH:D053609), weight loss (MESH:D015431), edema (MESH:D004487), labored breathing (MESH:D048949), atrophy (MESH:D001284), lung injury (MESH:D055370), hemorrhagic shock (MESH:D012771), cardiovascular complications (MESH:D002318), endothelial dysfunction (MESH:D014652), GI damage (MESH:D005767), BM (MESH:D001855), influenza (MESH:D007251), CBC (MESH:D006402), shock (MESH:D012769), injury to (MESH:D014947), fatty (MESH:D008067), Inflammatory (MESH:D007249), fibrosis (MESH:D005355), tumor metastasis (MESH:D009362), pulmonary and neurological disorders (MESH:D009422), IR (MESH:D011832), sepsis (MESH:D018805), cervical dislocation (MESH:D002575), TBI (MESH:D012793), neurological deficits (MESH:D009461), ischemia (MESH:D007511), storm (MESH:C566109), respiratory distress (MESH:D012128), Hematopoietic and Gastrointestinal Injury (MESH:D019337), BM aplasia (MESH:D019046), splenic injury (MESH:D013158), acute kidney injury (MESH:D058186), marrow aplasia (MESH:C566720), ARS (MESH:D054508), multi-organ failure (MESH:D009102), abdominal sepsis (MESH:D000007), hemorrhage (MESH:D006470), mucosal damage (MESH:D052016)
- **Chemicals:** VT (MESH:C000613371), PEG (MESH:D011092), CRB1001060 (-), paraffin (MESH:D010232), H&amp;E (MESH:D006371), ethanol (MESH:D000431), formalin (MESH:D005557), ROS (MESH:D017382), PBS (MESH:D007854), 60Co (MESH:C000615395), H (MESH:D006859), isoflurane (MESH:D007530), CO2 (MESH:D002245)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941350/full.md

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Source: https://tomesphere.com/paper/PMC12941350