This Coronavirus Disease 2019 (COVID-19) supplement will study the role of neutrophil extracellular traps (NETs) as biomarkers and therapeutic targets in COVID-19. The supplement will preserve the parent project?s focus on ectoenzymes and purinergic signaling as amplifiable counterpoints to neutrophil hyperactivity and exaggerated NET release (NETosis). Indeed, elevated levels of blood neutrophils are an early indicator of SARS-CoV-2 infection, where they predict severe COVID-19 respiratory disease. Our group and others have recently revealed a critical role for NETs in various thrombo-inflammatory states including sepsis, venous thrombosis, and respiratory failure. NETs are extracellular tangles of chromatin, microbicidal proteins, and oxidant enzymes that are released by neutrophils to corral infections; however, when not properly regulated, NETs have potential to amplify inflammation and thrombosis. In COVID-19, we hypothesize that NETs will function as powerful biomarkers for predicting progression to respiratory failure. With special relevance to this application, a recent study performed in China suggested potential efficacy of the adenosine-receptor agonist, dipyridamole in severe cases of COVID-19. Dipyridamole is an FDA-approved drug that our group recently discovered?through work on the parent project?to inhibit NETosis via activation of adenosine A2A receptors (A2AR). The hypothesis here is that A2AR agonists such as dipyridamole will compensate for virus-mediated deficiencies in the pulmonary ACE2 axis and thereby suppress NETosis. This supplement requests funds to support three complementary Aims.
Aim 1 will determine the extent to which NET levels can be used as predictive biomarkers in COVID-19.
Aim 2 will elucidate mechanisms by which the ACE2/angiotensin-(1-7) axis regulates COVID-19 neutrophils. Finally, Aim 3 will determine the extent to which adenosine receptor agonism prevents NETosis and macrophage activation in COVID-19.

Public Health Relevance

In some patients with COVID-19 (the disease caused by SARS-CoV-2), symptoms can rapidly progress to a life-threatening respiratory illness, which is driven by a virus-provoked inflammatory storm. We hypothesize that neutrophils, the most abundant type of white blood cell in circulation, are central to the propagation of that storm. Our group is uniquely positioned to leverage what we have learned about neutrophils in other thrombotic and inflammatory diseases to establish better biomarkers for severe COVID-19, and to develop new personalized approaches for preventing progression to the severest forms of the condition.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
3R01HL134846-03S2
Application #
10144599
Study Section
Program Officer
Mcdonald, Cheryl
Project Start
2020-05-01
Project End
2021-07-31
Budget Start
2020-08-15
Budget End
2021-07-31
Support Year
3
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Knight, Jason S; Mazza, Levi F; Yalavarthi, Srilakshmi et al. (2018) Ectonucleotidase-Mediated Suppression of Lupus Autoimmunity and Vascular Dysfunction. Front Immunol 9:1322