The understanding of the immunopathology in COVID-19 infection
dc.authorid | Didem Akal Taşcıoğlu / 0000-0003-2172-2611 | |
dc.authorscopusid | Didem Akal Taşcıoğlu / 39362314000 | |
dc.authorwosid | Didem Akal Taşcıoğlu / GMU-4600-2022 | |
dc.contributor.author | Akal Taşcıoğlu, Didem | |
dc.contributor.author | Akkaya, Emre | |
dc.contributor.author | Genc, Sema | |
dc.date.accessioned | 2021-05-28T10:38:27Z | |
dc.date.available | 2021-05-28T10:38:27Z | |
dc.date.issued | 2021 | en_US |
dc.department | İstinye Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü | en_US |
dc.description.abstract | Coronaviruses belonging to the Coronaviridae family are single-stranded RNA viruses. The entry of SARS-CoV-2 is accomplished via ACE-2 receptors. SARS-CoV-2 infection coactivates both innate and adaptive immune responses. Although SARS-CoV-2 stimulates antibody production with a typical pattern of IgM/IgG, cellular immunity is also impaired. In severe cases, low CD4 + and CD8 + T cell counts are associated with impaired immune functions, and high neutrophil/lymphocyte ratios accompanying low lymphocyte subsets have been demonstrated. Recently, high IFN -?/? ratios with impaired T cell responses, and increased IL-1, IL-6, TNF-?, MCP-1, IP-10, IL-4, IL-10 have been reported in COVID-19 infection. Increased proinflammatory cytokines and chemokines in patients with severe COVID-19 may cause the suppression of CD4 + and CD8 + T cells and regulatory T cells, causing excessive inflammatory responses and fatal cytokine storm with tissue and organ damage. Consequently, novel therapeutics to be developed against host immune system, including blockade of cytokines (IL-6, IL-1, IFN) themselves, their receptors or signaling pathways- JAK inhibitors- could be effective as potential therapeutics. | en_US |
dc.identifier.citation | Tascioglu, D., Akkaya, E., & Genc, S. (2021). The understanding of the immunopathology in COVID-19 infection. Scandinavian journal of clinical and laboratory investigation, 1–9. Advance online publication. https://doi.org/10.1080/00365513.2021.1892817 | en_US |
dc.identifier.doi | 10.1080/00365513.2021.1892817 | en_US |
dc.identifier.endpage | 9 | en_US |
dc.identifier.issn | 0036-5513 | en_US |
dc.identifier.issn | 1502-7686 | en_US |
dc.identifier.pmid | 34032527 | en_US |
dc.identifier.scopus | 2-s2.0-85106524178 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 1 | en_US |
dc.identifier.uri | https://doi.org/10.1080/00365513.2021.1892817 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12713/1763 | |
dc.identifier.wos | WOS:000654051800001 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Akal Taşcıoğlu, Didem | |
dc.language.iso | en | en_US |
dc.publisher | Taylor & Francis Online | en_US |
dc.relation.ispartof | Scandinavian Journal of Clinical and Laboratory Investigation | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | COVID-19 | en_US |
dc.subject | Chemokines | en_US |
dc.subject | Cytokines | en_US |
dc.subject | Immunotherapy | en_US |
dc.subject | Pandemics | en_US |
dc.title | The understanding of the immunopathology in COVID-19 infection | en_US |
dc.type | Article | en_US |