
International Journal of Infectious Diseases, Год журнала: 2024, Номер unknown, С. 107271 - 107271
Опубликована: Окт. 1, 2024
Язык: Английский
International Journal of Infectious Diseases, Год журнала: 2024, Номер unknown, С. 107271 - 107271
Опубликована: Окт. 1, 2024
Язык: Английский
Microbiology Spectrum, Год журнала: 2024, Номер 12(3)
Опубликована: Фев. 6, 2024
ABSTRACT It is urgently needed to evaluate the necessity and benefits of booster vaccination against coronavirus 2 severe acute respiratory syndrome (SARS-CoV-2) Omicron facilitate clinical decision-making for 2019 disease (COVID-19) convalescents. We conducted a multicenter, prospective trial (registration number: ChiCTR2100045810) in first patients with COVID-19 from 28 January 2020 20 February assess long-term durability neutralizing antibodies live BA.5 further efficiency safety CoronaVac convalescent group. A total 96 convalescents were enrolled this study. Neutralizing antibody titers significantly reduced 9–10 months. dose-refreshing an titer below induced by 4.84-fold. Meanwhile, abundance naive T cells increased dramatically, EMRA EM gradually decreased after vaccination. Activation-induced cell death apoptosis-related genes elevated all T-cell subtypes. One-dose was effective inducing robust response SARS-CoV-2 low titers. However, vaccine-mediated consumption regeneration patterns may be detrimental antiviral response. IMPORTANCE The globally dominant variant raises possibility repeat infections among importance multicenter study lies its evaluation efficacy Omicron. findings suggest that one-dose also highlights potential effects on due patterns. These results are crucial facilitating informing public health policies regarding vaccinations.
Язык: Английский
Процитировано
0bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown
Опубликована: Март 4, 2024
Abstract Several effective vaccines for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have been developed and implemented in the population. However, current production capacity falls short of meeting global demand. Therefore, it is crucial to further develop novel vaccine platforms that can bridge distribution gap. AVX/COVID-12 a vector-based utilizes Newcastle Disease virus (NDV) present SARS-CoV-2 spike protein immune system. This study analyses antigenicity candidate by examining antibody binding T-cell activation individuals infected with or variants concern (VOCs), as well healthy volunteers who received disease 2019 (COVID-19) vaccinations. Our findings indicate effectively binds antibodies activates T-cells 3 doses BNT162b2 AZ/ChAdOx-1-S vaccines. Furthermore, stimulation from patients recipients resulted their proliferation secretion interferon-gamma (IFN-γ) both CD4+ CD8+ T-cells. In conclusion, vectored demonstrates ability stimulate robust cellular responses recognized primed viruses patients, mRNA These results support inclusion booster vaccination programs aimed at addressing COVID-19 caused its VOCs.
Язык: Английский
Процитировано
0Research Square (Research Square), Год журнала: 2024, Номер unknown
Опубликована: Март 22, 2024
Язык: Английский
Процитировано
0bioRxiv (Cold Spring Harbor Laboratory), Год журнала: 2024, Номер unknown
Опубликована: Июль 3, 2024
ABSTRACT Vaccines have historically played a pivotal role in controlling epidemics. Effective vaccines for viruses causing significant human disease, e.g ., Ebola, Lassa fever, or Crimean Congo hemorrhagic fever virus, would be invaluable to public health strategies and counter-measure development missions. Here, we propose coverage metrics quantify vaccine-induced CD8 + T cell-mediated immune protection, as well characterize immuno-dominant epitopes, light of genetic heterogeneity viral evolution. Proof-of-principle our approach methods will demonstrated Ebola SARS-CoV-2, Burkholderia pseudomallei (vaccine) proteins.
Язык: Английский
Процитировано
0International Journal of Infectious Diseases, Год журнала: 2024, Номер unknown, С. 107271 - 107271
Опубликована: Окт. 1, 2024
Язык: Английский
Процитировано
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