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Review
. 2022 Jun:104:1-12.
doi: 10.1016/j.clinbiochem.2022.03.002. Epub 2022 Mar 17.

The importance of neopterin in COVID-19: The prognostic value and relation with the disease severity

Affiliations
Review

The importance of neopterin in COVID-19: The prognostic value and relation with the disease severity

Yousef Rasmi et al. Clin Biochem. 2022 Jun.

Abstract

Coronavirus Disease 2019 [COVID-19], caused by severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2], has rapidly evolved into a global health emergency. Neopterin [NPT], produced by macrophages when stimulated with interferon [IFN-]gamma, is an essential cytokine in the antiviral immune response. NPT has been used as a marker for the early assessment of disease severity in different diseases. The leading cause of NPT production is the pro-inflammatory cytokine IFN-. Macrophage activation has also been revealed to be linked with disease severity in SARS-CoV-2 patients. We demonstrate the importance of NPT in the pathogenesis of SARS-CoV-2 and suggest that targeting NPT in SARS-CoV-2 infection may be critical in the early prediction of disease progression and provision of timely management of infected individuals.

Keywords: COVID-19; Neopterin; Prognosis; SARS CoV-2.

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Conflict of interest statement

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

None
Graphical abstract
Fig. 1
Fig. 1
Biosynthesis of neopterin: IFN-γ activates GTP cyclo-hydrolase that further cleaves GTP to 7,8-dihydro-neopterin triphosphate, and phosphatases, in turn, change this intermediate to neopterin. Since humans lack PTPS, an enzyme that converts DHNTP into 5,6,7,8-tetra hydrobiopetrin, the DHNTP is only biosynthesized to neopterin. On the other hand, IFN-γ initiates tryptophan degradation to kynurenine by activating the IDO enzyme. Thus, there is a direct correlation between increased neopterin and tryptophan degradation.
Fig. 2
Fig. 2
Zn can inhibit ACE2 expression by reducing sirtuin1.
Fig. 3
Fig. 3
HOCI mechanism acting on pathogens.

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