A Novel Soluble ACE2 Protein Provides Lung and Kidney Protection in Mice Susceptible to Lethal SARS-CoV-2 Infection. Issue 7 (July 2022)

• Record Type: Journal Article
• Authors: Hassler, Luise; Wysocki, Jan; Gelarden, Ian; Sharma, Isha; Tomatsidou, Anastasia; Ye, Minghao; Gula, Haley; Nicoleascu, Vlad; Randall, Glenn; Pshenychnyi, Sergii; Khurram, Nigar; Kanwar, Yashpal; Missiakas, Dominique; Henkin, Jack; Yeldandi, Anjana; Batlle, Daniel
• Is Part Of: Journal of the American Society of Nephrology. Volume 33:Issue 7(2022)
• Page Start: 1293
• Page End: 1307
• Publication Date: 2022-07
• Subjects: virology -- kidney disease -- renin angiotensin system -- acute renal failure -- renal protection -- mice -- COVID-19 -- SARS-CoV-2 -- angiotensin-converting enzyme 2 -- disease susceptibility
• DOI: 10.1681/ASN.2021091209
• Languages: English
• ISSNs: 1046-6673

Abstract

Significance Statement: A novel soluble angiotensin converting enzyme 2 (ACE2) protein with increased binding to the spike protein of the coronavirus that causes coronavirus disease 2019 (COVID-19) is protective in an animal model of severe COVID-19, providing a proof of concept of efficacy. Administration of soluble ACE2 protein resulted in conversion of a lethal disease into a mild one that is reversible, with improved lung and kidney injury. Visual Abstract: Abstract : Background: Severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) uses full-length angiotensin converting enzyme 2 (ACE2) as a main receptor to enter target cells. The goal of this study was to demonstrate the preclinical efficacy of a novel soluble ACE2 protein with increased duration of action and binding capacity in a lethal mouse model of COVID-19. Methods: A human soluble ACE2 variant fused with an albumin binding domain (ABD) was linked via a dimerization motif hinge-like 4-cysteine dodecapeptide (DDC) to improve binding capacity to SARS-CoV-2. This novel soluble ACE2 protein (ACE2–1-618-DDC-ABD) was then administered intranasally and intraperitoneally to mice before intranasal inoculation of SARS-CoV-2 and then for two additional days post viral inoculation. Results: Untreated animals became severely ill, and all had to be humanely euthanized by day 6 or 7 and had pulmonary alveolar hemorrhage with mononuclear infiltrates. In contrast, all but one mouse infected with a lethal dose of SARS-CoV-2 that received ACE2–1-618-DDC-ABD survived. In the animals inoculated with SARS-CoV-2 that were untreated, viral titers were high in the lungs and brain, but viral titers were absent in the kidneys. Some untreated animals, however, had variable degrees of kidney proximal tubular injury as shown by attenuation of the proximal tubular brush border and increased NGAL and TUNEL staining. Viral titers in the lung and brain were reduced or nondetectable in mice that received ACE2–1-618-DDC-ABD, and the animals developed only moderate disease as assessed by a near-normal clinical score, minimal weight loss, and improved lung and kidney injury. Conclusions: This study demonstrates the preclinical efficacy of a novel soluble ACE2 protein, termed ACE2–1-618-DDC-ABD, in a lethal mouse model of SARS-CoV-2 infection that develops severe lung injury and variable degrees of moderate kidney proximal tubular injury.