TY - JOUR
T1 - Evidence for and against direct kidney infection by SARS-CoV-2 in patients with COVID-19
AU - Hassler, Luise
AU - Reyes, Fabiola
AU - Sparks, Matthew A.
AU - Welling, Paul
AU - Batlle, Daniel
N1 - Funding Information:
We wish to acknowledge productive discussions over the last several months on the topic of this paper with various members of the COVID-19 and ACE2 in Cardiovascular, Lung, and Kidney Working Group composed of Matthew A. Sparks, Swapnil Hiremath, Daniel Batlle, Andrew South, Paul Welling, J. Matt Luther, Jordana Cohen, James Brian Byrd, Louise M. Burrell, Laurie Tomlinson, Vivek Bhalla, MarıaJose Soler, and Sundar Swaminathan.
Funding Information:
D.C. Batlle reports consultancy agreements with, and receiving honoraria from, AstraZeneca, Relypsa, and Tricida; reports receiving research funding from AstraZeneca, the Feinberg Foundation, and National Institute of Diabetes and Digestive and Kidney Diseases; reports serving as a scientific advisor or member of Relypsa and Tricida; reports being a founder and main owner of Angiotensin Therapeutics Inc., with no royalties or income at this time; reports being coinventor of an issued patent “Active Low Molecular Weight Variants of Angiotensin Converting Enzyme 2,” and provisional patents “Active low molecular weight variants of Angiotensin Converting Enzyme 2 (ACE2) for the treatment of diseases and conditions of the eye” and “Shorter soluble forms of Angiotensin Converting Enzyme 2 (ACE2) for treating and preventing coronavirus infection.” M.A. Sparks reports employment with Duke University and Durham Veterans Affairs Health Care System; reports receiving research funding from Renal Research Institute; and reports receiving honoraria from Elsevier for Nephrology Secrets. M.A. Sparks reports serving as a scientific advisor or member of American Board of Internal Medicine, Nephrology Board, Board of Director, NephJC, and the Editorial Boards of American Journal of Kidney Diseases, ASN Kidney News, Kidney360, and Kidney Medicine; Council for the Kidney in Cardiovascular Disease (KCVD) Membership & Communications Committee American Heart Association (AHA); KCVD Scientific & Clinical Education Lifelong Learning Committee AHA; and National Kidney Foundation (NKF) North Carolina Medical Advisory Board. P. Welling reports receiving research funding from LeDucq Foundation and National Institutes of Health; reports receiving honoraria from the American Physiological Society; reports serving on the Editorial Board of American Journal of Physiology-Renal Physiology, chair of the American Physiological Society Finance Committee, and Chair of Kidney Molecular Biology and Development, National Institutes of Health. All remaining authors have nothing to disclose.
Publisher Copyright:
© 2021 by the American Society of Nephrology.
PY - 2021/11
Y1 - 2021/11
N2 - Despite evidence of multiorgan tropism of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in patients with coronavirus disease 2019 (COVID-19), direct viral kidney invasion has been difficult to demonstrate. The question of whether SARS-CoV2 can directly infect the kidney is relevant to the understanding of pathogenesis of AKI and collapsing glomerulopathy in patients with COVID-19. Methodologies to document SARS-CoV-2 infection that have been used include immunohistochemistry, immunofluorescence, RT-PCR, in situ hybridization, and electron microscopy. In our review of studies to date, we found that SARS-CoV-2 in the kidneys of patients with COVID-19 was detected in 18 of 94 (19%)by immunohistochemistry, 71 of 144 (49%) by RT-PCR, and 11 of 84 (13%)byin situ hybridization. In a smaller number of patients with COVID-19 examined by immunofluorescence, SARS-CoV-2 was detected in 10 of 13 (77%). In total, in kidneys from 102 of 235 patients (43%), the presence of SARS-CoV-2 was suggested by at least one of the methods used. Despite these positive findings, caution is needed because many other studies have been negative for SARS-CoV-2 and it should be noted that when detected, it was only in kidneys obtained at autopsy. There is a clear need for studies from kidney biopsies, including those performed at early stages of the COVID-19–associated kidney disease. Development of tests to detect kidney viral infection in urine samples would be more practical as a noninvasive way to evaluate SARS-CoV-2 infection during the evolution of COVID-19–associated kidney disease.
AB - Despite evidence of multiorgan tropism of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in patients with coronavirus disease 2019 (COVID-19), direct viral kidney invasion has been difficult to demonstrate. The question of whether SARS-CoV2 can directly infect the kidney is relevant to the understanding of pathogenesis of AKI and collapsing glomerulopathy in patients with COVID-19. Methodologies to document SARS-CoV-2 infection that have been used include immunohistochemistry, immunofluorescence, RT-PCR, in situ hybridization, and electron microscopy. In our review of studies to date, we found that SARS-CoV-2 in the kidneys of patients with COVID-19 was detected in 18 of 94 (19%)by immunohistochemistry, 71 of 144 (49%) by RT-PCR, and 11 of 84 (13%)byin situ hybridization. In a smaller number of patients with COVID-19 examined by immunofluorescence, SARS-CoV-2 was detected in 10 of 13 (77%). In total, in kidneys from 102 of 235 patients (43%), the presence of SARS-CoV-2 was suggested by at least one of the methods used. Despite these positive findings, caution is needed because many other studies have been negative for SARS-CoV-2 and it should be noted that when detected, it was only in kidneys obtained at autopsy. There is a clear need for studies from kidney biopsies, including those performed at early stages of the COVID-19–associated kidney disease. Development of tests to detect kidney viral infection in urine samples would be more practical as a noninvasive way to evaluate SARS-CoV-2 infection during the evolution of COVID-19–associated kidney disease.
UR - http://www.scopus.com/inward/record.url?scp=85119035722&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85119035722&partnerID=8YFLogxK
U2 - 10.2215/CJN.04560421
DO - 10.2215/CJN.04560421
M3 - Article
C2 - 34127485
AN - SCOPUS:85119035722
SN - 1555-9041
VL - 16
SP - 1755
EP - 1765
JO - Clinical journal of the American Society of Nephrology : CJASN
JF - Clinical journal of the American Society of Nephrology : CJASN
IS - 11
ER -