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Targeting TNF-α for COVID-19: Recent Advanced and Controversies

Yi Guo, Ke Hu, Yuxuan Li, Chanjun Lu, Ken Ling, Chuanqi Cai, Weici Wang, Dawei Ye

2022Frontiers in Public Health132 citationsDOIOpen Access PDF

Abstract

Recent advances in the pathophysiologic understanding of coronavirus disease 2019 (COVID-19) suggests that cytokine release syndrome (CRS) has an association with the severity of disease, which is characterized by increased tumor necrosis factor α (TNF-α), interleukin (IL)-6, IL-2, IL-7, and IL-10. Hence, managing CRS has been recommended for rescuing severe COVID-19 patients. TNF-α, one of the pro-inflammatory cytokines commonly upregulated in acute lung injury, triggers CRS and facilitates SARS-CoV-2 interaction with angiotensin-converting enzyme 2 (ACE2). TNF-α inhibitors, therefore, may serve as an effective therapeutic strategy for attenuating disease progression in severe SARS-CoV-2 infection. Below, we review the possibilities and challenges of targeting the TNF-α pathway in COVID-19 treatment.

Topics & Concepts

Tumor necrosis factor alphaCoronavirus disease 2019 (COVID-19)MedicineAngiotensin-converting enzyme 2Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)DiseaseImmunologyCytokinePathophysiology2019-20 coronavirus outbreakCoronavirusTumor necrosis factor αBioinformaticsVirologyInternal medicineInfectious disease (medical specialty)BiologyOutbreakCOVID-19 Clinical Research StudiesLong-Term Effects of COVID-19Inflammasome and immune disorders