Caffeic acid phenetyl ester and its ability to prevent viral infection - Some comments

نویسنده

  • Salvatore Chirumbolo
چکیده

A recent paper by Erdemli et al. on this journal reviewed the antiviral properties of caffeic acid phenetyl ester (CAPE) [1]. Recent literature showed that CAPE has also anti-inflammatory and immune-modulatory effects, as like as many other plant-derived phenolics [2] but its ability to exert an anti-inflammatory role has never been assessed in clinical trials, therefore, its activity on humans appears only presumptive. Yet, biomedical literature about CAPE effect on chronic inflammation and cancer appears quite promising and should encourage randomized controlled trials in patients. Its ability to affect in-vitro tumors is not so far than many other plant-derived phenolics, considered as anti-NF-κB agents [3], yet its antiviral potential might be attributed to independent pathways from interferon (IFN) induced by virus entry [4]. If CAPE is described only as an inhibitor of NF-κB activation, then some controversial issues would be raised. It is well-known that cells activate host-pathogen interactions, through the recognition of pathogen-associated molecular patterns by host sensors, which were defined as pattern recognition receptors. They include toll-like receptors (TLRs), RIG-I-like receptors (RLRs), NOD-like receptors (NLRs), and DNA receptors. Then, virus may trigger these innate immune receptors. In the cell response, the activation of the nuclear factor-κB (NF-κB) transcription pathway is crucial for the immediate early step of immune activation. However, there are a variety of viral effectors that have been shown to prevent NF-κB signalling, namely, they should act as polyphenols at least three different levels: (a) TLRs, IκB kinase complexes and at the transcriptional level [5]. The antiviral activity of CAPE might be more complex than expected, therefore, as it might interfere with innate immunity as like as viruses, if it should act only on NF-κB, even by preventing its activation [5]. Which are the major targets of CAPE within an infected or inflamed cell? The paper by Erdemli et al. report some interesting suggestions [1]. Further consideration should be made. As many other phenol-bearing molecules from plant biochemistry, CAPE should exert a protective role for plants and a proto-toxic activity in animals. CAPE has been described in the past to possess a prooxidant activity [6], particularly in the range 1.0-0.5 μM, interestingly the same range reported for its antiviral potential [4]. This apparently contradictory evidence, where CAPE is both a pro-oxidant and an antiviral molecule, deserves further considerastion about the many targets of CAPE activity and its pleiotropism within a defined cell. The paper by Erdemli …

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عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2016