| Literature DB >> 33707532 |
Gozde Sir Karakus1, Cihan Tastan1,2, Derya Dilek Kancagi1, Bulut Yurtsever1, Gamze Tumentemur3, Sevda Demir4, Raife Dilek Turan1,4, Selen Abanuz1,5, Didem Cakirsoy1,6, Utku Seyis1, Samed Ozer7, Omer Elibol8, Muhammer Elek1,4, Gurcan Ertop3, Serap Arbak9, Merve Acikel Elmas9, Cansu Hemsinlioglu1, Ayse Sesin Kocagoz10, Ozden Hatirnaz Ng11, Sezer Akyoney11,12, Ilayda Sahin6,13, Ugur Ozbek13, Dilek Telci4, Fikrettin Sahin4, Koray Yalcin1,14, Siret Ratip15, Ercument Ovali16.
Abstract
COVID-19 outbreak caused by SARS-CoV-2 created an unprecedented health crisis since there is no vaccine for this novel virus. Therefore, SARS-CoV-2 vaccines have become crucial for reducing morbidity and mortality. In this study, in vitro and in vivo safety and efficacy analyzes of lyophilized vaccine candidates inactivated by gamma-irradiation were performed. The candidate vaccines in this study were OZG-3861 version 1 (V1), an inactivated SARS-CoV-2 virus vaccine, and SK-01 version 1 (V1), a GM-CSF adjuvant added vaccine. The candidate vaccines were applied intradermally to BALB/c mice to assess toxicity and immunogenicity. Preliminary results in vaccinated mice are reported in this study. Especially, the vaccine models containing GM-CSF caused significant antibody production with neutralization capacity in absence of the antibody-dependent enhancement feature, when considered in terms of T and B cell responses. Another important finding was that the presence of adjuvant was more important in T cell in comparison with B cell response. Vaccinated mice showed T cell response upon restimulation with whole inactivated SARS-CoV-2 or peptide pool. This study shows that the vaccines are effective and leads us to start the challenge test to investigate the gamma-irradiated inactivated vaccine candidates for infective SARS-CoV-2 virus in humanized ACE2 + mice.Entities:
Year: 2021 PMID: 33707532 DOI: 10.1038/s41598-021-83930-6
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379