SBIR/STTR Research Award

CD73 for sepsis

Award identifier bc7d24e636820b17fd3ed6f6aa4e59c098041f8cb762083ed264fb9c6e7c262dAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$225,000

Program and phase

STTR · Phase I

Award year

2020

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Purine Pharmaceuticals Inc.
Proposal award date
2020-04-07
Contract end date
2021-03-31
UEI
K1FBL8EVSSK6
Solicitation number
PA19-270
Topic code
NIAID

Research abstract

SUMMARYSepsis is a medical condition caused by an overwhelming systemic inflammatory response to infection. Although the underlying infection can now be efficiently treated with antibiotics, there are no effective therapies to control the organ damage caused by the inflammatory response of the host. As a result, sepsis is the leading cause of mortality in intensive care units and is the tenth leading cause of death overall in the US. CD73 or ecto-5andapos;-nucleotidase is a cell surface-associated anti-inflammatory enzyme. It has multiple anti- inflammatory actions, which are mediated by triggering the production of the anti-inflammatory agent adenosine. Using CD73 deficient mice and pharmacological antagonists, we have discovered that endogenous CD73 protects mice against polymicrobial sepsis-induced inflammation, organ damage, and mortality. Based on these results, we propose exogenously administered human recombinant soluble CD73 (hsCD73) as a novel and effective therapy for sepsis. Our hypothesis is that treatment of mice with human recombinant soluble CD73 would reduce inflammation, organ damage, and mortality in sepsis. To address this hypothesis, we propose two Specific Aims. In Specific Aim 1, we will test the efficacy of hsCD73 in preventing mortality in polymicrobial sepsis induced by cecal ligation and puncture in mice. In Specific Aim 2, we will delineate the effect of hsCD73 on inflammation and organ injury in sepsis. We expect that hsCD73 will reduce inflammation, organ damage, and mortality in septic mice. The long-term goal of this study is to develop hsCD73 as a safe and effective treatment option for the management of patients with sepsis.NARRATIVESepsis remains the leading cause of mortality and morbidity in critically ill patients, because it triggers an overwhelming inflammatory response in the host. In the proposed studies, we will test a human recombinant soluble ecto-5andapos;-nucleotidase or CD73, which has broad anti-inflammatory effects, for efficacy in protecting against organ damage, inflammation and mortality in sepsis. The long-term goal is to develop soluble CD73 as a safe and effective therapeutic intervention for sepsis patients.

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

6 SBIR/STTR records share this UEI (2017–2023). Reported award amounts total $1,393,806. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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