R01AI156037
Project Grant
Overview
Grant Description
Chronic Wasting Disease Vaccines - Project Summary / Abstract
No prophylactic or therapeutic regimen is known for any prion disease. The BSE outbreak in cattle, with the subsequent emergence of a new and transmissible human prion disease (VCJD), highlights the public health threat from prion diseases. The commonalities among mammalian prion diseases are quite remarkable.
The ongoing and expanding major threat from prion disease in North America is Chronic Wasting Disease (CWD). CWD is an emergent rapidly spreading disease in cervids, with uncertain zoonotic potential. Approximately 9 million Americans hunt deer and elk, with an estimated 7,000-15,000 CWD-infected cervids consumed annually (increasing 20% per year). As hunting is a roughly $26 billion per annum industry, CWD also represents an enormous potential health and economic threat.
We have developed novel vaccine strategies which show promise in animal models and have established a carefully-graded CWD challenge, in tandem with a longitudinal monitoring system in our unique indoor-housed white-tailed deer facility, permitting CWD vaccine assessment in the native host.
We propose 3 aims to determine the ability of homologous or heterologous immunization strategies to protect deer from CWD infection and mitigate prion shedding. In Aim 1, we will determine the efficacy and safety of CWD vaccines that have complementary targets, a highly innovative and rationally designed vaccine which targets PRPSC and a second vaccine strategy which aims at eliminating the substrate for prion conversion, and whether combining the vaccines is more effective. In Aim 2, we will determine if these vaccine strategies, alone or in combination, protect deer from CWD infection. Aim 3 will further determine if vaccination reduces prion shedding in excreta and secreta (urine, feces, and saliva) of CWD challenged deer, thereby reducing infection between cervids and environmental contamination.
The translational impact of the results of these studies will:
A) Develop prototype vaccine candidates for prion diseases
B) Provide management tools for the cervid industry and wildlife management
C) Mitigate the risks of zoonotic transmission of cervid prions.
Thereby, this research will have immediate impacts in both human and animal health.
No prophylactic or therapeutic regimen is known for any prion disease. The BSE outbreak in cattle, with the subsequent emergence of a new and transmissible human prion disease (VCJD), highlights the public health threat from prion diseases. The commonalities among mammalian prion diseases are quite remarkable.
The ongoing and expanding major threat from prion disease in North America is Chronic Wasting Disease (CWD). CWD is an emergent rapidly spreading disease in cervids, with uncertain zoonotic potential. Approximately 9 million Americans hunt deer and elk, with an estimated 7,000-15,000 CWD-infected cervids consumed annually (increasing 20% per year). As hunting is a roughly $26 billion per annum industry, CWD also represents an enormous potential health and economic threat.
We have developed novel vaccine strategies which show promise in animal models and have established a carefully-graded CWD challenge, in tandem with a longitudinal monitoring system in our unique indoor-housed white-tailed deer facility, permitting CWD vaccine assessment in the native host.
We propose 3 aims to determine the ability of homologous or heterologous immunization strategies to protect deer from CWD infection and mitigate prion shedding. In Aim 1, we will determine the efficacy and safety of CWD vaccines that have complementary targets, a highly innovative and rationally designed vaccine which targets PRPSC and a second vaccine strategy which aims at eliminating the substrate for prion conversion, and whether combining the vaccines is more effective. In Aim 2, we will determine if these vaccine strategies, alone or in combination, protect deer from CWD infection. Aim 3 will further determine if vaccination reduces prion shedding in excreta and secreta (urine, feces, and saliva) of CWD challenged deer, thereby reducing infection between cervids and environmental contamination.
The translational impact of the results of these studies will:
A) Develop prototype vaccine candidates for prion diseases
B) Provide management tools for the cervid industry and wildlife management
C) Mitigate the risks of zoonotic transmission of cervid prions.
Thereby, this research will have immediate impacts in both human and animal health.
Awardee
Funding Goals
TO ASSIST PUBLIC AND PRIVATE NONPROFIT INSTITUTIONS AND INDIVIDUALS TO ESTABLISH, EXPAND AND IMPROVE BIOMEDICAL RESEARCH AND RESEARCH TRAINING IN INFECTIOUS DISEASES AND RELATED AREAS, TO CONDUCT DEVELOPMENTAL RESEARCH, TO PRODUCE AND TEST RESEARCH MATERIALS. TO ASSIST PUBLIC, PRIVATE AND COMMERCIAL INSTITUTIONS TO CONDUCT DEVELOPMENTAL RESEARCH, TO PRODUCE AND TEST RESEARCH MATERIALS, TO PROVIDE RESEARCH SERVICES AS REQUIRED BY THE AGENCY FOR PROGRAMS IN INFECTIOUS DISEASES, AND CONTROLLING DISEASE CAUSED BY INFECTIOUS OR PARASITIC AGENTS, ALLERGIC AND IMMUNOLOGIC DISEASES AND RELATED AREAS. PROJECTS RANGE FROM STUDIES OF MICROBIAL PHYSIOLOGY AND ANTIGENIC STRUCTURE TO COLLABORATIVE TRIALS OF EXPERIMENTAL DRUGS AND VACCINES, MECHANISMS OF RESISTANCE TO ANTIBIOTICS AS WELL AS RESEARCH DEALING WITH EPIDEMIOLOGICAL OBSERVATIONS IN HOSPITALIZED PATIENTS OR COMMUNITY POPULATIONS AND PROGRESS IN ALLERGIC AND IMMUNOLOGIC DISEASES. BECAUSE OF THIS DUAL FOCUS, THE PROGRAM ENCOMPASSES BOTH BASIC RESEARCH AND CLINICAL RESEARCH. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM EXPANDS AND IMPROVES PRIVATE SECTOR PARTICIPATION IN BIOMEDICAL RESEARCH. THE SBIR PROGRAM INTENDS TO INCREASE AND FACILITATE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. THE SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM STIMULATES AND FOSTERS SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. RESEARCH CAREER DEVELOPMENT AWARDS SUPPORT THE DEVELOPMENT OF SCIENTISTS DURING THE FORMATIVE STAGES OF THEIR CAREERS. INDIVIDUAL NATIONAL RESEARCH SERVICE AWARDS (NRSAS) ARE MADE DIRECTLY TO APPROVE APPLICANTS FOR RESEARCH TRAINING IN SPECIFIED BIOMEDICAL SHORTAGE AREAS. IN ADDITION, INSTITUTIONAL NATIONAL RESEARCH SERVICE AWARDS ARE MADE TO ENABLE INSTITUTIONS TO SELECT AND MAKE AWARDS TO INDIVIDUALS TO RECEIVE TRAINING UNDER THE AEGIS OF THEIR INSTITUTIONAL PROGRAM.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Fort Collins,
Colorado
805214593
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 395% from $716,065 to $3,544,335.
Colorado State University was awarded
Chronic Wasting Disease Vaccines: Novel Strategies for CWD Protection
Project Grant R01AI156037
worth $3,544,335
from the National Institute of Allergy and Infectious Diseases in July 2021 with work to be completed primarily in Fort Collins Colorado United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.855 Allergy and Infectious Diseases Research.
The Project Grant was awarded through grant opportunity NIH Research Project Grant (Parent R01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 8/6/25
Period of Performance
7/8/21
Start Date
6/30/26
End Date
Funding Split
$3.5M
Federal Obligation
$0.0
Non-Federal Obligation
$3.5M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01AI156037
Transaction History
Modifications to R01AI156037
Additional Detail
Award ID FAIN
R01AI156037
SAI Number
R01AI156037-1903492242
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Funding Office
75NM00 NIH National Institute of Allergy and Infectious Diseases
Awardee UEI
LT9CXX8L19G1
Awardee CAGE
4B575
Performance District
CO-02
Senators
Michael Bennet
John Hickenlooper
John Hickenlooper
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Allergy and Infectious Diseases, National Institutes of Health, Health and Human Services (075-0885) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,417,885 | 100% |
Modified: 8/6/25