Immunogenic middle east respiratory syndrome coronavirus (MERS-CoV) compositions and methods
An immunogenic and compositional technology, applied in the field of generating high-affinity antibodies, can solve problems such as limiting widespread availability
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Embodiment 1
[0133] Generation of MERSCoV spike nanoparticles
[0134] Nanoparticles were generated by overexpressing the MERSCoV spike protein in baculovirus (Figures 8 and 9) in Sf9 cells. After purification, spike protein-containing nanoparticle VLPs were mainly recovered as trimers ( Figure 4 and 6 ).
Embodiment 2
[0136] Induction of immune responses using MERSCoV spike nanoparticles
[0137] Administration of VLPs to mice, such as Figure 5 displayed in . At the end of the 45 day period, blood was drawn from the mice to assess the immune response. Figure 7 Neutralizing antibody titers of mice administered with SARS-CoV spike nanoparticle VLPs or MERS-CoV spike nanoparticle VLPs are shown. The highest response was obtained by using the adjuvant matrix M1.
Embodiment 3
[0139] Potent anti-MERS-CoV human immunoglobulin generated from autotransgenic bovine inhibits MERS-CoV in vivo
[0140] To demonstrate that anti-MERSCoV hIgG antibodies and immunoglobulins obtained from Tc cattle after vaccination can neutralize MERSCoV in vitro and in vivo, we administered three experimental MERSCoV vaccines to three separate Tc cattle herds to induce high titer against MERSCoV neutralizing antibodies. The first vaccine tested was a whole killed Jordan strain (clade A) MERS-CoV virion (WKV) vaccine and the second was an Al-Hasa (clade B) MERS-CoV spike nanoparticle (SN ) vaccine, while the third is the Al-HasaMERS-CoV spike protein pDNA vaccine. The pDNA vaccine was found to be poorly immunogenic by in vitro assays and was not evaluated further (data not presented). However, convalescent sera and highly purified hIgG immunoglobulins from both WKV (designated SAB-300) and SN (designated SAB-301) vaccinated Tc cattle were able to cross-neutralize the virus i...
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