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Post Challenge Effects of Ozg-38.61.3 Gamma Irradiated SARS-CoV-2 Vaccine on Organ Protection in Transgenic Mouse Model

dc.contributor.authorOztatlici, Mustafa
dc.contributor.authorKancagi, Derya Dilek
dc.contributor.authorOztatlici, Hulya
dc.contributor.authorTuran, Raife Dilek
dc.contributor.authorKarakus, Gozde Sir
dc.contributor.authorYurtsever, Bulut
dc.contributor.authorCakirsoy, Didem
dc.contributor.authorAbanuz, Selen
dc.contributor.authorTastan, Cihan
dc.contributor.authorOzer, Samed
dc.contributor.authorTumentemur, Gamze
dc.contributor.authorKasap, Murat
dc.contributor.authorAkpinar, Gurler
dc.contributor.authorHalicioglu, Busra Sen
dc.contributor.authorDemir, Sevda
dc.contributor.authorTelci, Dilek
dc.contributor.authorSahin, Fikrettin
dc.contributor.authorTuglu, Mehmet Ibrahim
dc.contributor.authorOvali, Ercument
dc.date.accessioned2026-11-05T11:00:23Z
dc.date.issued2025
dc.description.abstractObjective: Coronavirus disease 2019 (COVID-19) is an infectious outbreak caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and virus-related deaths are increasing day by day. For this reason, vaccine studies and their urgent use are of great importance to prevent the pandemic. In this study, multi-organ damages caused by SARS-CoV-2 virus in human-angiotensin-converting enzyme type 2 (ACE2) transgenic mice and the protective effects of OZG-38.61.3 gamma irradiated SARS-CoV-2 vaccine against viral damage were investigated. Methods: For this purpose, transgenic K18-hACE2 BALB/c mice were randomly allocated into 4 groups, negative control group (NC), positive control group (PC, SARS-CoV-2 infected), and 2 different doses of OZG-38.61.3 vaccine (Challenge 1, dose of 1013 and Ch2, 1014 viral particle after SARS-CoV-2 infection). Afterthe administrations, lung, heart and kidneytissues were examined by histopathological, immunohistochemical and TUNEL analysis. Results: Our results showed that the vaccine doses decreased the apoptosis, oxidative stress and inflammation parameters caused by virus in lung, heart, and kidney tissues. It was also found that the vaccine protected the expressions of tight junction proteins in the kidneys. Conclusion: According to our findings, it is suggested that the OZG-38.61.3 can be an effective and protective vaccine that can be safely used against the SARS-CoV-2 virus.
dc.description.issue3
dc.description.pages504-516
dc.description.sponsorshipFunding: The author (s) received no financial support for the research. All funding in the work was supported by Celltek Health and Consulting Services Limited Company.
dc.description.volume15
dc.identifier.doi10.33808/clinexphealthsci.1512385
dc.identifier.issn2459-1459
dc.identifier.urihttps://doi.org/10.33808/clinexphealthsci.1512385
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10416
dc.identifier.wosWOS:001593250700006
dc.language.isoen
dc.publisherMARMARA UNIV, INST HEALTH SCIENCES
dc.relation.fundingCelltek Health and Consulting Services Limited Company
dc.relation.hasversion10.33808/clinexphealthsci.1512385
dc.relation.ispartofCLINICAL AND EXPERIMENTAL HEALTH SCIENCES
dc.subjectCOVID-19
dc.subjectSARS-CoV-2
dc.subjecthuman ACE2 transgenic mouse
dc.subjectOrgan damage
dc.subjectVaccination
dc.subjectMICE
dc.subjectMedicine, Research & Experimental
dc.subjectResearch & Experimental Medicine
dc.titlePost Challenge Effects of Ozg-38.61.3 Gamma Irradiated SARS-CoV-2 Vaccine on Organ Protection in Transgenic Mouse Model
dc.typeArticle
oaire.citation.editionEmerging Sources Citation Index (ESCI)
oaire.citation.endPage516
oaire.citation.issue3
oaire.citation.startPage504
oaire.citation.volume15
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