Project Grant R01HL178801
- The National Heart, Lung, and Blood Institute awarded $448,250 to The Research Foundation For The State University Of New York on May 15, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837) to develop and evaluate a lung-targeted immunomodulatory messenger RNA therapy for acute respiratory distress syndrome. The award funds development of an IL-10 mRNA therapeutic delivered via sulfonium lipid nanoparticles, a novel lung-targeting technology designed to suppress...
- The National Heart, Lung, and Blood Institute awarded the University of Illinois $670,622 as a Project Grant (R01HL180941) on July 15, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837). The award funds research into the role of endogenous RNA sensing in the amplification of lung injury. The research focuses on how lung infections induce widespread lung vascular endothelial injury through a cycle of endothelial barrier breakdown and inflammatory cell influx. The project...
- The National Institutes of Health National Heart Lung and Blood Institute awarded The Washington University $635,247 on September 1, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837) to investigate the role of resolution-phase neutrophils in acute respiratory distress syndrome (ARDS) recovery. The project tests the hypothesis that neutrophils activate counter-regulatory mechanisms, including expression of 15-lipoxygenase (15-LO), in lung tissue following acute injury to...
- The National Heart, Lung, and Blood Institute awarded Weill Medical College of Cornell University $1,541,783 on September 15, 2025, under the Cardiovascular Diseases Research program (CFDA 93.837) to investigate novel roles of the thrombin receptor protease-activated receptor-1 (PAR1) in lung lymphatic function and acute respiratory distress syndrome. The research uses mouse models to examine PAR1's role in button junction formation during lung injury. The work identifies how...
- The National Heart, Lung, and Blood Institute awarded the University of California, San Diego $778,127 on September 1, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837, Project Grant R01HL180797) to enhance lamellar body function via LRRK2 inhibition and reduce respiratory distress syndrome severity in preterm newborns. The research investigates leucine-rich repeat kinase 2 (LRRK2) inhibition as a novel therapeutic approach to enhance endogenous surfactant production in...
- The National Heart, Lung, and Blood Institute awarded the University of Rochester $717,611 on September 1, 2026, as a Project Grant (R01HL184442) under the Cardiovascular Diseases Research program (CFDA 93.837) to investigate protective mechanisms in lung vascular injury associated with acute lung injury and acute respiratory distress syndrome. The research establishes MIRO1, a mitochondrial Rho GTPase, as a mechanistic link in preserving endothelial cell barrier integrity and restoring cell...
- The National Heart, Lung, and Blood Institute awarded The Feinstein Institutes for Medical Research $586,866 on May 15, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837) to investigate the protective role of B-1a cells in acute lung injury and to evaluate a novel therapeutic compound. The project examines the mechanisms by which B-1a cells mitigate acute lung injury and acute respiratory distress syndrome, conditions frequently triggered by sepsis or ischemia-reperfusion...
- The National Institutes of Health National Heart Lung and Blood Institute awarded Ann & Robert H Lurie Children's Hospital of Chicago $781,860 on September 1, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837) to investigate the novel role of neutrophils in mediating endothelial regeneration and vascular repair in sepsis and acute respiratory distress syndrome (ARDS). The research addresses ARDS pathology, specifically endothelial barrier injury and increased vascular...
- The National Heart, Lung, and Blood Institute awarded Duke University $2,023,862 on September 15, 2025, under the Cardiovascular Diseases Research program (CFDA 93.837, Assistance Listing R01HL170175) to develop and validate predictive models of acute respiratory distress syndrome (ARDS) using protein biomarkers and clinical data, and to identify resilience markers and endotypes associated with ARDS recovery through an integrated multiomics pipeline. The project, titled "Resilience...
- The National Heart, Lung, and Blood Institute awarded the University of Arizona $748,677 on September 1, 2026, under the Cardiovascular Diseases Research program (CFDA 93.837) to develop nanoparticle delivery systems targeting lung endothelial cell repair in pediatric acute respiratory distress syndrome (ARDS). The research addresses the lack of innovative molecular approaches to pediatric ARDS management by engineering lung endothelial cell-specific nanoparticle carriers capable of delivering...
The National Heart, Lung, and Blood Institute awarded the University of Georgia Research Foundation, Inc. $588,284 on August 1, 2026, to investigate long noncoding RNA regulation in complement-mediated endothelial barrier disruption as a potential therapeutic strategy for acute lung injury and acute respiratory distress syndrome. Award R01HL178801 is funded under the Cardiovascular Diseases Research program (CFDA 93.837), a Project Grant. The research addresses the persistent 30–40% mortality rate in acute respiratory distress syndrome despite five decades of diagnostic and therapeutic development. The project focuses on endothelial cell death as a critical pathological event in the disease; damage to pulmonary capillary endothelial cells compromises the alveolar-capillary barrier, resulting in increased vascular permeability, pulmonary edema, and impaired gas exchange. The recipient identified a long noncoding RNA, lncenc1, that is markedly upregulated in murine lungs following bacterial infection. The research demonstrates that lncenc1 deficiency confers protection against Klebsiella pneumoniae-induced lung injury and pulmonary edema, suggesting that targeting long noncoding RNA mechanisms of endothelial cell death may offer a novel approach to improve outcomes in patients with acute lung injury and acute respiratory distress syndrome. Performance occurs in Athens, Georgia. The period of performance extends from August 1, 2026, through April 30, 2031.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $588.3k | 8/3/26 |