CONTROVERSIAL ROLE OF ACE2 IN SARS-COV-2 INFECTION: A LITERATURE REVIEW

Authors

  • Andréia Michelle Alves Cunha de Alcântara Author
  • Ivan de Alcântara Barbosa Barros Author
  • Ivan Barbosa Barros Author
  • Maria de Mascena Diniz Maia Author
  • Paulo Roberto Eleutério de Souza Author

DOI:

https://doi.org/10.56238/arev7n7-062

Keywords:

Severe Acute Respiratory Syndrome, Angiotensin Converting Enzyme 2, Coronavirus disease, Renin-Angiotensin-Aldosterone System, Coronavirus

Abstract

Bibliographic Review: Coronavirus-19 Disease (COVID-19) presents a clinical spectrum from oligosymptomatic to severe and multisystemic inflammation, which may be followed by death. SARS-CoV-2, the virus responsible for COVID-19, has as its main human receptor the Angiotensin-Converting Enzyme 2 (ACE2), which is also crucial in the control of the inflammatory response, through the Renin-Angiotensin-Aldosterone System ( RAAS). Objective:  Due to the controversial roles of ACE2 in SARS-CoV-2 infection, the aim of this literature review was to address its distribution in the human body, associating it with the severity of COVID-19. Thus, using the terms ACE2, SARS-CoV-2 and Coronavirus, a search was performed on the SciELO, PubMed and Scopus platforms. The research revealed that the aggressiveness of SARS-CoV-2 is related to its ability to interact with the host and, consequently, with ACE2 - widely distributed in organs and tissues. Final Considerations: However, since COVID-19 is an inflammatory disease, and ACE2 is critical in controlling inflammation, especially in RAAS, the data compiled in this review infers that ACE2 is more likely to act as a protective factor, against the severity of COVID-19.

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Published

2025-07-04

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Articles

How to Cite

DE ALCÂNTARA, Andréia Michelle Alves Cunha; BARROS, Ivan de Alcântara Barbosa; BARROS, Ivan Barbosa; MAIA, Maria de Mascena Diniz; DE SOUZA, Paulo Roberto Eleutério. CONTROVERSIAL ROLE OF ACE2 IN SARS-COV-2 INFECTION: A LITERATURE REVIEW. ARACÊ , [S. l.], v. 7, n. 7, p. 36264–36286, 2025. DOI: 10.56238/arev7n7-062. Disponível em: https://periodicos.newsciencepubl.com/arace/article/view/6390. Acesso em: 17 jul. 2025.