SBIR/STTR Research Award

Development of swine model of COPD by integrating genetic and environmental risk factors

Award identifier 72f5555476d0516398914223883abfc88c1be3cffa390719f4c44c6d91d93a0dAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$398,696

Program and phase

SBIR · Phase I

Award year

2017

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Recombinetics, Inc.
Proposal award date
2017-09-15
Contract end date
2019-09-14
UEI
L99NWZNZ7K57
Solicitation number
PA16-180
Topic code
100

Research abstract

PROJECT SUMMARY lpha antitrypsin AAT deficiency AATD and Chronic Obstructive Pulmonary Disease COPD are lung diseases both of which share phenotypic features including airflow obstruction and airway mucociliary dysfunction attributed primarily to emphysema a condition that defines damage and enlargement of the air sacs of the lungs causing breathlessness AATD is the major genetic cause of early onset COPD typically exacerbated by cigarette smoking There is still no cure for AATD COPD associated emphysema no treatment can reverse the damage to the lungs Prevalence of COPD is increasing significantly warranting need for new therapies Lack of a proper animal model that mimics the human disease has been a constraint owing to structural and functional differences between human and rodent lungs We propose that pigs with a genetic model of emphysema in conjunction with exposure to cigarette smoke CS could provide consistent pulmonary tissue alterations that are characteristic features of AATD COPD This swine model will be of great value for pre clinical research and facilitate development of innovative treatments to slow stop or reverse the damage to the lungs caused by AATD COPD For that we plan to generate pigs with AATD the only defined genetic risk factor of emphysema AATD is caused by a mutation of the protease inhibitor PI gene resulting in a reduced level of AAT in blood and lung leading to breakdown of the lung tissue by the enzyme neutrophil elastase We intend to utilize our novel gene editing platform to develop swine with the most prevalent and severe AATD genotype PI ZZ Accordingly the pig model with the PI ZZ mutant genotype will develop emphysema a characteristic feature of AATD PI ZZ mutant genotype will be exposed to CS to intensify the AATD phenotype to COPD PI ZZ Then this Realization of this mutant genotype will be monitored by serological testing in vivo while progression of emphysema is evaluated clinically and confirmed pathomorphlogically We believe that such a reliable large animal model of AATD COPD linked emphysema will have tremendous impact on industry and academic research to develop and test new drugs and novel therapeutic approaches to treat AATD COPD associated emphysema PROJECT NARRATIVE Emphysema is a classic feature of lung diseases lpha antitrypsin AAT deficiency AATD and Chronic Obstructive Pulmonary Disease COPD This SBIR aims to develop a swine emphysema model using gene editing to mimic the most common and severe allele of AATD PI ZZ mutation observed in human patients These gene edited pigs will be exposed to the major cause of COPD cigarette smoke to simulate both genetic and environmental risk factors There is still no cure for AATD COPD associated emphysema no treatments proven to reverse the damage to the lungs and without transplant all patientsandapos progress into severe pulmonary failure We propose that this unique large animal model will more accurately mimic the human condition and accelerate translation of novel therapies into the clinic

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

20 SBIR/STTR records share this UEI (2011–2024). Reported award amounts total $9,634,813. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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