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The potential involvement of P2X7 receptor in COVID-19 pathogenesis: A new therapeutic target?

Journal

SCANDINAVIAN JOURNAL OF IMMUNOLOGY
Volume 93, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1111/sji.12960

Keywords

COVID-19; immunopathogenesis; NLRP3 inflammasome; SARS-CoV-2

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Research suggests that the pathogenesis of COVID-19 may involve a hyperinflammatory response, with the activation of cytokines such as IL-1β and the NLRP3 inflammasome. The recognition of extracellular ATP by the P2X7 receptor may be related to immune dysregulation caused by the SARS-CoV-2 infection.
Coronavirus disease 2019 (COVID-19) pathogenesis remains under investigation. Growing evidence indicates the establishment of a hyperinflammatory response, characterized by sustained production of cytokines, such as IL-1 beta. The release and maturation of this cytokine are dependent on the activation of a catalytic multiprotein complex, known as inflammasome. The most investigated is the NLRP3 inflammasome, which can be activated by various stimuli, such as the recognition of extracellular ATP by the P2X7 receptor. Based on the recent literature, we present evidence that supports the idea that the P2X7R/NLRP3 axis may be involved in the immune dysregulation caused by the SARS-CoV-2 infection.

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