Litcius/Paper detail

COX2 inhibition in the treatment of COVID-19: Review of literature to propose repositioning of celecoxib for randomized controlled studies

Semih Bağhaki, Can Ege Yalçın, Sema Bağhaki, Servet Yekta Aydın, Başak Dağhan, Ersin Yavuz

2020International Journal of Infectious Diseases69 citationsDOIOpen Access PDF

Abstract

Coronavirus-triggered pulmonary and systemic disease, i.e. systemic inflammatory response to virally triggered lung injury, named COVID-19, and ongoing discussions on refining immunomodulation in COVID-19 without COX2 inhibition prompted us to search the related literature to show a potential target (COX2) and a weapon (celecoxib). The concept of selectively targeting COX2 and closely related cascades might be worth trying in the treatment of COVID-19 given the substantial amount of data showing that COX2, p38 MAPK, IL-1b, IL-6 and TGF-β play pivotal roles in coronavirus-related cell death, cytokine storm and pulmonary interstitial fibrosis. Considering the lack of definitive treatment and importance of immunomodulation in COVID-19, COX2 inhibition might be a valuable adjunct to still-evolving treatment strategies. Celecoxib has properties that should be evaluated in randomized controlled studies and is also available for off-label use.

Topics & Concepts

Cytokine stormCelecoxibCoronavirus disease 2019 (COVID-19)MedicineRandomized controlled trialPulmonary fibrosisIntensive care medicineSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)2019-20 coronavirus outbreakFibrosisDiseasePharmacologyInternal medicinePathologyInfectious disease (medical specialty)OutbreakCancer, Stress, Anesthesia, and Immune ResponsePharmacological Receptor Mechanisms and EffectsSynthesis and biological activity