key: cord-343766-hlg7t5i5
authors: Vinken, Mathieu
title: A putative AOP for pneumonia related to COVID-19
date: 2020-07-20
journal: Arch Toxicol
DOI: 10.1007/s00204-020-02860-w
sha: 
doc_id: 343766
cord_uid: hlg7t5i5

nan

insight into the mechanism of the cellular entry of viral particles and to support vaccine development. In order to further encourage research in this direction, an updated version of the putative AOP for pneumonia linked to COVID-19 is proposed, which encompasses new knowledge that is rapidly accumulating (Fig. 1) . One of the major MIEs in this AOP is the binding of SARS-CoV-2 to the angiotensin-converting enzyme 2 (ACE2) receptor at the plasma membrane surface of type II pneumocytes lining the alveoli in lung. This binding occurs through subunit S1 of the SARS-CoV-2 surface spike glycoprotein S, with the latter being primed by cellular transmembrane serine protease 2 (TMPRSS2) (Xiao et al. 2020) . Upon entry, which involves internalization of both SARS-CoV-2 and the ACE2 receptor, the virus replicates by making use of the ribosomes of the host cell and by relying on the actions of RNA replicase. Following assembly of the de novo synthetized viral proteins, the newly formed SARS-CoV-2 is released and propagates infection (Tu et al. 2020 ). The process of viral replication triggers an inflammatory response accompanied by the recruitment of macrophages. This most likely involves activation of the NOD-like receptor family pyrin domain-containing 3 (NLRP3) inflammasome, which facilitates the production of pro-inflammatory cytokines, including interleukin 1β and interleukin 18. NLRP3 induces the formation of gasdermin-D pores on the plasma membrane surface, causing secretion of interleukin 1β and interleukin 18 as well as the influx of water into the cytosol, which in turn leads to cell swelling and subsequent rupture or so-called pyroptosis (Yap et al. 2020 ). The released pro-inflammatory cytokines, along with changes in angiotensin homeostasis, compromise the structure and functionality of surrounding endothelial cells in alveolar vasculature. In particular, permeability becomes increased and goes hand in hand with endothelial fluid leakage and the occurrence of edema (Leisman et al. 2020 ). Simultaneously, released pro-inflammatory cytokines stimulate the generation of reactive oxygen and nitrogen species, and thus the onset of oxidative stress (Ntyonga-Pono 2020). In parallel, several enzyme systems, in particular proteases, are activated, which damage cellular architecture. Collectively, 1 3 these deteriorating events instigate consolidation, denoting the replacement of air in the alveoli by transudate, pus, blood or cells, which presents as the typical "white lungs" during radiography. This may or may not coincide with collapse of the lung or so-called atelectasis The outcome of this is reduced or even absent gas exchange and hence respiratory failure (Gallelli et al. 2020) . This is ultimately manifested clinically as dry cough and shortness of breath, also called tussis and dyspnea, respectively (Öztürk 2020), being considered as the actual adverse outcome (AO).

It should be stressed that this proposed AOP must be considered with caution, as it has not been assessed according to the tailored Bradford-Hill criteria to evaluate biological plausibility, essentiality and empirical support (Becker et al. 2015) . Indeed, the relevance and sequence of some KEs as well as their links may not be fully substantiated by current information. Inherent to their dynamic nature, AOPs should be updated and finetuned as soon as new relevant data become available. This certainly holds true for the AOP for pneumonia linked to COVID-19. In fact, the proposed AOP should eventually evolve into an AOP network that considers all clinically pertinent MIEs and AOs. A number of efforts towards this goal are currently ongoing, including at the European Commission's Joint Research Center (JRC). Such AOP network should comprise the mechanisms driving the multi-organ failure frequently observed in severe COVID-19 patients, for which the causes (i.e. MIEs) are as yet not entirely clear or delineated. Thus, liver failure may be caused by the direct binding and actions of SARS-CoV-2 in hepatocytes or cholangiocytes, but could also be an indirect consequence of the systemic inflammatory response syndrome associated with COVID-19. In addition, liver failure may result from hepatic injury caused by drugs administered to COVID-19 patients (Alqahtani and Schattenberg 2020) . The future COVID-19 AOP network could also cover the different steps of virus infection and, especially, replication, now captured in a single KE. This could be of specific relevance for the development of novel drugs and vaccines, which typically target this process. The overall COVID-19 AOP network could serve a number of purposes, a prominent one being disease modeling. In this respect, an appealing opportunity lies ahead to generate animal-free new approach methodologies (NAMs) that allow to study particular aspects of the COVID-19 spectrum (Busquet et al. 2020) . By optimally combining these NAMs, mechanistically anchored in the AOP network, further insight into COVID-19 pathogenesis will be gained, which in turn will open perspectives for setting up targeted clinical treatment strategies.

Conflict of interest The author declares that he has no conflict of interest.

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