Host sphingolipids: Perspective immune adjuvant for controlling SARS-CoV-2 infection for managing COVID-19 disease
dc.contributor.author | Prakash, Hridayesh | |
dc.contributor.author | Upadhyay, Dilip | |
dc.contributor.author | Bandapalli, Obul Reddy | |
dc.contributor.author | Jain, Aklank | |
dc.contributor.author | Kleuser, Burkhard | |
dc.date.accessioned | 2024-01-21T10:44:34Z | |
dc.date.accessioned | 2024-08-13T13:22:18Z | |
dc.date.available | 2024-01-21T10:44:34Z | |
dc.date.available | 2024-08-13T13:22:18Z | |
dc.date.issued | 2020-11-02T00:00:00 | |
dc.description.abstract | Sphingolipids are potent bioactive agents involved in the pathogenesis of various respiratory bacterial infections. To date, several sphingolipid derivatives are known, but S1P (Sphingosine-1-phosphate) and Ceramide are the best-studied sphingolipid derivatives in the context of human diseases. These are membrane-bound lipids that influence host-pathogen interactions. Based on these features, we believe that sphingolipids might control SARS-CoV-2 infection in the host. SARS-CoV-2 utilizes the ACE-II receptor (Angiotensin-converting enzyme II receptor) on epithelial cells for its entry and replication. Activation of the ACE-II receptor is indirectly associated with the activation of S1P Receptor 1 signaling which is associated with IL-6 driven fibrosis. This is expected to promote pathological responses during SARS-CoV-2 infection in COVID-19 cases. Given this, mitigating S1P signaling by application of either S1P Lyase (SPL) or S1P analog (Fingolimod / FTY720) seems to be potential approach for controlling these pathological outcomes. However, due to the immunosuppressive nature of FTY720, it can modulate hyper-inflammatory responses and only provide symptomatic relief, which may not be sufficient for controlling the novel COVID-19 infection. Since Th1 effector immune responses are essential for the clearance of infection, we believe that other sphingolipid derivatives like Cermaide-1 Phosphate with antiviral potential and adjuvant immune potential can potentially control SARS-CoV-2 infection in the host by its ability in enhancing autophagy and antigen presentation by DC to promote T cell response which can be helpful in controlling SARS-CoV-2 infection in novel COVID-19 patients. � 2020 | en_US |
dc.identifier.doi | 10.1016/j.prostaglandins.2020.106504 | |
dc.identifier.issn | 10988823 | |
dc.identifier.uri | http://10.2.3.109/handle/32116/3790 | |
dc.identifier.url | https://linkinghub.elsevier.com/retrieve/pii/S1098882320300976 | |
dc.language.iso | en_US | en_US |
dc.publisher | Elsevier Inc. | en_US |
dc.subject | Covid 19 | en_US |
dc.subject | Immune adjuvants | en_US |
dc.subject | M1/M2 macrophages | en_US |
dc.subject | Sphingolipids | en_US |
dc.subject | Th1 effector response | en_US |
dc.title | Host sphingolipids: Perspective immune adjuvant for controlling SARS-CoV-2 infection for managing COVID-19 disease | en_US |
dc.title.journal | Prostaglandins and Other Lipid Mediators | en_US |
dc.type | Review | en_US |
dc.type.accesstype | Open Access | en_US |