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Published on: November 5, 2021
Angiotensin-converting enzyme as a new immunologic target for the new SARS-CoV-2
Shahin Hallaj1,2, Anahita Ghorbani1, Seyed Ali Mousavi-Aghdas1
1Department of Basic Science, Faculty of Medicine, Maragheh University of Medical Sciences, Maragheh, Iran.
Insights
This study explores how renin-angiotensin-aldosterone system inhibitors (RASis) may impact COVID-19 by examining their role in inflammation and the angiotensin-converting enzyme II (ACE II) pathway. Further research is needed to confirm their therapeutic potential.
Area of Science:
- Immunology
- Pharmacology
- Infectious Diseases
Background:
- COVID-19 causes severe hyperinflammation and acute respiratory distress syndrome (ARDS) via cytokine release syndrome (CRS).
- Angiotensin-converting enzyme II (ACE II) is the viral entry point and plays a role in inflammation, with altered levels linked to poor COVID-19 prognosis.
- Renin-angiotensin-aldosterone system inhibitors (RASis) are used for conditions that are risk factors for severe COVID-19.
Purpose of the Study:
- To review the immunologic roles of the renin-angiotensin-aldosterone system (RAS) and RAS inhibitors (RASis).
- To discuss the molecular and immunologic aspects of RASis.
- To explore the potential significance of RASis in managing COVID-19.
Main Methods:
- Literature review of recent evidence on RAS, RASi, and their immunologic interactions.
- Analysis of molecular and immunologic mechanisms.
- Discussion of potential therapeutic implications for COVID-19.
Main Results:
- The renin-angiotensin-aldosterone system (RAS) and its inhibitors (RASis) have complex roles in immunologic interactions.
- ACE II levels and their modulation by RASis may influence COVID-19 pathogenesis.
- Evidence suggests a hypothetical basis for considering RASis in COVID-19 treatment.
Conclusions:
- RASis may modulate inflammatory responses relevant to COVID-19.
- Understanding the interplay between RAS, ACE II, and inflammation is crucial for COVID-19 therapeutics.
- Further clinical studies are warranted to evaluate the efficacy and safety of RASis in COVID-19 patients.
Abstract:
The coronavirus disease 2019 (COVID-19) pandemic has affected the daily lives of millions of people worldwide and had caused significant mortality; hence, the assessment of therapeutic options is of great interest. The leading cause of death among COVID-19 patients is acute respiratory distress syndrome caused by hyperinflammation secondary to cytokine release syndrome (CRS). Cytokines, such as tumor necrosis factor-α, interleukin-6, interferon-γ and interleukin-10, are the main mediators of CRS. Based on recent evidence, the angiotensin-converting enzyme (ACE) II is known to be the target of the COVID-19 spike protein, which enables the virus to penetrate human cells. ACE II also possesses an anti-inflammatory role in many pathologies such as cardiovascular disease, hypertension, diabetes mellitus and other conditions, which are the main risk factors of poor prognosis in COVID-19 infection. Changes in tissue ACE II levels are associated with many diseases and hyperinflammatory states, and it is assumed that elevated levels of ACE II could aggravate the course of COVID-19 infection. Therefore, the use of renin-angiotensin-aldosterone system inhibitors (RASis) in COVID-19 patients could be hypothetically considered, though sufficient evidence is not presented by the scientific community. In this work, based on the most recent pieces of evidence, the roles of RAS and RASi in immunologic interactions are addressed. Furthermore, the molecular and immunologic aspects of RASi and their potential significance in COVID-19 are discussed.
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