CD147-spike protein interaction in COVID-19: Get the ball rolling with a novel receptor and therapeutic target.

Abstract

The combat against the Corona virus disease of 2019 (COVID-19), has created a chaos among the healthcare institutions and researchers, in turn accelerating the dire need to curtail the infection spread. The already established entry mechanism, via ACE2 has not yet successfully aided in the development of a suitable and reliable therapy. Taking in account the constant progression and deterioration of the cases worldwide, a different perspective and mechanistic approach is required, which has thrown light onto the cluster of differentiation 147 (CD147) transmembrane protein, as a novel route for SARS-CoV-2 entry. Despite lesser affinity towards COVID-19 virus, as compared to ACE2, this receptor provides a suitable justification behind elevated blood glucose levels in infected patients, retarded COVID-19 risk in women, enhanced susceptibility in geriatrics, greater infection susceptibility of T cells, infection prevalence in non-susceptible human cardiac pericytes and so on. The manuscript invokes the title role and distribution of CD147 in COVID-19 as an entry receptor and mediator of endocytosis-promoted entry of the virus, along with the "catch and clump" hypothesis, thereby presenting its Fundamental significance as a therapeutic target for potential candidates, such as Azithromycin, melatonin, statins, beta adrenergic blockers, ivermectin, Meplazumab etc. Thus, the authors provide a comprehensive review of a different perspective in COVID-19 infection, aiming to aid the researchers and virologists in considering all aspects of viral entry, in order to develop a sustainable and potential cure for the 2019 COVID-19 disease.

• Authors: Tapan Behl, Ishnoor Kaur, Lotfi Aleya, Aayush Sehgal, Sukhbir Singh, Neelam Sharma, Saurabh Bhatia, Ahmed Al-Harrasi, Simona Bungau
• Journal: The Science of the total environment (Sci Total Environ) Vol. 808 Pg. 152072 (Feb 20 2022) ISSN: 1879-1026 [Electronic] Netherlands
• PMID: 34863742 (Publication Type: Journal Article, Review)
• Copyright: Copyright © 2021 Elsevier B.V. All rights reserved.

Chemical References

• Antibodies, Monoclonal, Humanized
• BSG protein, human
• Spike Glycoprotein, Coronavirus
• spike protein, SARS-CoV-2
• meplazumab
• Basigin

Topics

• Antibodies, Monoclonal, Humanized
• Basigin
• COVID-19
• Cell Differentiation
• Female
• Humans
• SARS-CoV-2
• Spike Glycoprotein, Coronavirus