Kidney Injury in COVID-19: Epidemiology, Molecular Mechanisms and Potential Therapeutic Targets

被引:19
|
作者
Teixeira, J. Pedro [1 ,2 ]
Barone, Sharon [1 ,3 ]
Zahedi, Kamyar [1 ,3 ]
Soleimani, Manoocher [1 ,3 ]
机构
[1] Univ New Mexico, Div Nephrol, Dept Internal Med, Hlth Sci Ctr, Albuquerque, NM 87131 USA
[2] Univ New Mexico, Div Pulm Crit Care & Sleep Med, Dept Internal Med, Hlth Sci Ctr, Albuquerque, NM 87131 USA
[3] New Mexico Vet Healthcare Med Ctr, Med Res Serv, Albuquerque, NM 87108 USA
关键词
SARS-CoV-2; COVID-19; acute kidney injury; CORONAVIRUS DISEASE 2019; ANGIOTENSIN-ALDOSTERONE SYSTEM; CRITICALLY-ILL PATIENTS; HOSPITALIZED-PATIENTS; CONVERTING ENZYME; SPIKE PROTEIN; FATAL COVID-19; SARS-COV-2; ACE2; RECEPTOR;
D O I
10.3390/ijms23042242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As of December 2021, SARS-CoV-2 had caused over 250 million infections and 5 million deaths worldwide. Furthermore, despite the development of highly effective vaccines, novel variants of SARS-CoV-2 continue to sustain the pandemic, and the search for effective therapies for COVID-19 remains as urgent as ever. Though the primary manifestation of COVID-19 is pneumonia, the disease can affect multiple organs, including the kidneys, with acute kidney injury (AKI) being among the most common extrapulmonary manifestations of severe COVID-19. In this article, we start by reflecting on the epidemiology of kidney disease in COVID-19, which overwhelmingly demonstrates that AKI is common in COVID-19 and is strongly associated with poor outcomes. We also present emerging data showing that COVID-19 may result in long-term renal impairment and delve into the ongoing debate about whether AKI in COVID-19 is mediated by direct viral injury. Next, we focus on the molecular pathogenesis of SARS-CoV-2 infection by both reviewing previously published data and presenting some novel data on the mechanisms of cellular viral entry. Finally, we relate these molecular mechanisms to a series of therapies currently under investigation and propose additional novel therapeutic targets for COVID-19.
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收藏
页数:23
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