Project Grant R21HL175177
- The University of Southern California (USC) Department of Contracts and Grants Division received a $413,958 Project Grant from the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837). The purpose of this 1-year award, effective September 22, 2023, is to investigate the role of the protein PUMA in promoting cell death and inflammation in chronic obstructive pulmonary disease (COPD) caused by cigarette smoke exposure. The research aims...
- Summary On September 15, 2025, the National Institute of Allergy and Infectious Diseases awarded Oasis Pharmaceuticals, LLC a $936,738 Project Grant under the Allergy and Infectious Diseases Research program (CFDA 93.855) for the development of PAR2 pepducins as a therapeutic treatment for chronic obstructive pulmonary disease (COPD). The award funds research through October 31, 2026, and supports the advancement of OA-235I, a cell-penetrating, lipidated protease-activated receptor-2 (PAR2)...
- Grant Award Summary The National Heart, Lung, and Blood Institute (NHLBI) awarded The Trustees of Columbia University in the City of New York $761,262 under the Cardiovascular Diseases Research program (CFDA 93.837) for a Project Grant commencing September 1, 2025, and concluding June 30, 2029. The research investigation will be conducted at Columbia's Health Sciences Division in New York, New York. This award funds a four-year basic science research project examining the protective mechanisms...
- Federal Grant Award Summary The National Heart, Lung, and Blood Institute (NHLBI) awarded the University of Pennsylvania a $683,564 project grant under the Cardiovascular Diseases Research program (CFDA 93.837) effective July 1, 2025, through March 31, 2030. The research project, titled "Alveolar Epithelial Stress Signaling in Lung Fibrosis," focuses on understanding the mechanisms underlying pulmonary fibrosis (PF), a progressive and devastating lung disease with limited therapeutic...
- Federal Project Grant Award Summary The National Heart, Lung, and Blood Institute (NHLBI) awarded Cleveland Clinic Lerner College of Medicine of Case Western Reserve University a project grant of $656,988 on August 1, 2025, under the Cardiovascular Diseases Research program (CFDA 93.837) to support research on the role of High Mobility Group Box 1 (HMGB1) in the lung response to bacterial injury. The research project, scheduled for completion by April 30, 2030, is designed to develop new...
- Federal Project Grant Award Summary Boston University Medical Campus received a $245,250 Project Grant from the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837), effective September 1, 2025, through May 31, 2029. The award funds research into novel mechanistic insights of inflammation and organ injury resulting from dysregulated host defense responses to bacterial pneumonia and sepsis. The project investigates circular RNA...
- Federal Project Grant Award Summary Emory University received a $794,661 project grant from the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837), awarded September 19, 2025, with completion targeted for June 30, 2030. The research initiative, titled "SMILE (Sickle Cell Disease Microbiologic and Immunologic Links to Health)," focuses on understanding how higher-order brain regions interact with brainstem circuits to...
- This Project Grant award of $389,754 from the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837) supports research to assess the therapeutic potential of a peptide derived from collagen XVIII for treating lung fibrosis associated with systemic sclerosis (scleroderma). The project aims to evaluate the anti-fibrotic effects of this peptide in a murine model of lung fibrosis, as well as identify the minimal effective dose, optimal...
- Federal Project Grant Award Summary The University of Pennsylvania received a $701,795 project grant from the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837), effective September 1, 2025, through June 30, 2029. The award funds a research project titled "Defining Cardinal Functions of Lung Progenitors During Regeneration," which investigates the mechanisms of lung tissue repair and regeneration following acute injury,...
- Grant Award Summary The University of California, San Francisco (UCSF) received a $182,060 Project Grant award from the National Heart, Lung, and Blood Institute (NHLBI) under the Cardiovascular Diseases Research program (CFDA 93.837), effective September 30, 2025 through November 29, 2026. The research project investigates the role of the senescence marker protein P16INK4A in alveolar epithelial stem cells during injury-triggered differentiation in the lung. Using a multi-transgenic mouse model...
ROLE OF SPECIALIZED PRO-RESOLVING MEDIATORS OF INFLAMMATION RESOLUTION IN EMPHYSEMA: ANALYSES OF SPIROMICS AND LEEP - PROJECT SUMMARY/ABSTRACT INFLAMMATION IS A CENTRAL PATHOLOGIC MECHANISM ACROSS A VARIETY OF CHRONIC DISEASES, INCLUDING CARDIOVASCULAR, METABOLIC, AND PULMONARY DISORDERS. CURRENT APPROACHES TO DISEASE MANAGEMENT CENTER ON NON-SPECIFIC STRATEGIES TO ATTENUATE LOCAL AND SYSTEMIC INFLAMMATION TO IMPROVE HEALTH OUTCOMES. HOWEVER, EMERGING DATA SUPPORTS THE PRESENCE OF ENDOGENOUS MECHANISMS INCREASING AN INDIVIDUAL'S CAPACITY TO RESOLVE INFLAMMATION, HIGHLIGHTING A YET UNTAPPED NOVEL THERAPEUTIC TARGET. NEW INSIGHTS INTO THE RESOLUTION OF INFLAMMATION REVEAL THIS PROCESS CAN BE MEDIATED BY LIPID-DERIVED SPECIALIZED PRO-RESOLVING MEDIATORS (SPMS), WHICH TRIGGER A CASCADE OF EVENTS THAT ATTENUATE THE INFLAMMATORY RESPONSE. SPMS HAVE BEEN IMPLICATED IN THE RESOLUTION OF INFLAMMATION IN A VARIETY OF DISEASES SUCH AS CARDIOVASCULAR DISEASE, COVID-19, AND ASTHMA; HOWEVER, THEIR ROLE IN RESOLVING INFLAMMATION AND COUNTERACTING LUNG INJURY IN COPD PATIENTS IS UNKNOWN. THE OBJECTIVE OF THIS PROPOSAL IS TO DETERMINE IF GREATER PLASMA CIRCULATING SPM CONCENTRATIONS (REFLECTING INDIVIDUAL CAPACITY TO RESOLVE INFLAMMATION) ARE ASSOCIATED WITH IMPROVED RESPIRATORY OUTCOMES IN INDIVIDUALS WITH EMPHYSEMA. TO ACCOMPLISH THIS, WE WILL LEVERAGE DATA FROM THE ROBUSTLY-PHENOTYPED AND DIVERSE SUBPOPULATIONS AND INTERMEDIATE OUTCOME MEASURES IN COPD STUDY (SPIROMICS) COHORT WITH AVAILABLE BIOSPECIMENS IN BIOLINCC. WE WILL THEN VALIDATE OUR FINDINGS IN THE LOSARTAN EFFECTS ON EMPHYSEMA PROGRESSION (LEEP) COHORT. THIS PROPOSAL WILL ACCOMPLISH THE FOLLOWING SPECIFIC AIMS: IN SA 1: WE WILL CHARACTERIZE CIRCULATING SPM CONCENTRATIONS AS A BIOMARKER FOR DECREASED POTENTIAL TO RESOLVE CHRONIC INFLAMMATION ACROSS TWO DIVERSE POPULATIONS OF EMPHYSEMA PATIENTS AND IDENTIFY RISK FACTORS (E.G.RACE/ETHNICITY, ECONOMIC DEPRIVATION, ETC.) FOR LOW SPM STATUS. WE HYPOTHESIZE THAT THERE WILL BE CLEAR DISPARITIES IN SPM ACROSS SUBPOPULATIONS REFLECTING DIFFERENCES IN RESILIENCE TO INFLAMMATORY INSULTS. IN SA 2: WE WILL DETERMINE THE ASSOCIATION BETWEEN CIRCULATING SPM CONCENTRATIONS AND COPD HEALTH OUTCOMES (I.E., LUNG FUNCTION, RESPIRATORY SYMPTOMS) ACROSS TWO POPULATIONS OF EMPHYSEMA PATIENTS. WE HYPOTHESIZE THAT GREATER SPM STATUS WILL BE ASSOCIATED WITH GREATER LUNG FUNCTION AND DECREASED RESPIRATORY MORBIDITY. THIS WORK IS DIRECTLY RELATED TO THE MISSION OF NHLBI AS IT WILL PROVIDE FOUNDATIONAL EVIDENCE FOR SPMS AS AN EMERGING THERAPEUTIC TARGET FOR THE PREVENTION AND TREATMENT OF COPD, STIMULATING BASIC DISCOVERIES ABOUT THE CAUSES OF, AND RESILIENCE FACTORS FOR, LUNG DISEASE AND ENABLING THE TRANSLATION OF THESE FINDINGS INTO CLINICAL PRACTICE.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $123.7k | 8/7/25 | ||
| Not listed | $139.1k | 7/25/24 |
GrantNumber | Description | Subgrantee | Prime Award | Dollars Obligated | Updated At |
|---|---|---|---|---|---|
0255J4014609S | Board Of Regents Of The University Of Nebraska | Project Grant R21HL175177 | $90.8k | 5/14/25 | |
0255J4014609S | Colorado State University | Project Grant R21HL175177 | $0 | 9/17/24 |