مورد إلكتروني

Vaccinia Virus Strain MVA Expressing a Prefusion-Stabilized SARS-CoV-2 Spike Glycoprotein Induces Robust Protection and Prevents Brain Infection in Mouse and Hamster Models

التفاصيل البيبلوغرافية
العنوان: Vaccinia Virus Strain MVA Expressing a Prefusion-Stabilized SARS-CoV-2 Spike Glycoprotein Induces Robust Protection and Prevents Brain Infection in Mouse and Hamster Models
بيانات النشر: Multidisciplinary Digital Publishing Institute 2023-05-21
تفاصيل مُضافة: Instituto de Salud Carlos III
Agencia Estatal de Investigación (España)
European Commission
CSIC - Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA)
San Antonio Medical Foundation
Texas Biomedical Forum
Lorenzo, Maria M. [0000-0001-7588-673X]
Marín-López, A. [0000-0003-2840-1722]
Chiem, Kevin [0000-0002-3892-5944]
Jiménez-Cabello, Luis [0000-0001-8085-5823]
Utrilla-Trigo, S. [0000-0002-7672-7658]
Calvo Pinilla, Eva María [0000-0002-4667-4081]
Lorenzo, Gema [0000-0003-1869-9051]
Moreno, Sandra [0000-0002-3548-037X]
Ye, Chengjin [0000-0002-1934-9494]
Matía, Alejandro [0000-0002-4246-5135]
Brun Torres, Alejandro [0000-0001-7865-538X]
Sánchez-Puig Eyre, Juana María [0000-0002-3966-3499]
Nogales, Aitor [0000-0002-2424-7900]
Mothes, Walther [0000-0002-3367-7240]
Uchil, Pradeep D. [0000-0002-7236-858X]
Kumar, Priti [0000-0002-6901-5601]
Ortego, Javier [0000-0002-4275-7277]
Fikrig, Erol [0000-0002-5884-6047]
Martínez-Sobrido, Luis [0000-0001-7084-0804]
Blasco Lozano, Rafael [0000-0002-8819-5767]
Lorenzo, Maria M.
Marín-López, A.
Chiem, Kevin
Jiménez-Cabello, Luis
Ullah, Irfan
Utrilla-Trigo, S.
Calvo Pinilla, Eva María
Lorenzo, Gema
Moreno, Sandra
Ye, Chengjin
Park, Jun-Gyu
Matía, Alejandro
Brun Torres, Alejandro
Sánchez-Puig Eyre, Juana María
Nogales, Aitor
Mothes, Walther
Uchil, Pradeep D.
Kumar, Priti
Ortego, Javier
Fikrig, Erol
Martínez-Sobrido, Luis
Blasco Lozano, Rafael
نوع الوثيقة: Electronic Resource
مستخلص: The COVID-19 pandemic has underscored the importance of swift responses and the necessity of dependable technologies for vaccine development. Our team previously developed a fast cloning system for the modified vaccinia virus Ankara (MVA) vaccine platform. In this study, we reported on the construction and preclinical testing of a recombinant MVA vaccine obtained using this system. We obtained recombinant MVA expressing the unmodified full-length SARS-CoV-2 spike (S) protein containing the D614G amino-acid substitution (MVA-Sdg) and a version expressing a modified S protein containing amino-acid substitutions designed to stabilize the protein a in a pre-fusion conformation (MVA-Spf). S protein expressed by MVA-Sdg was found to be expressed and was correctly processed and transported to the cell surface, where it efficiently produced cell-cell fusion. Version Spf, however, was not proteolytically processed, and despite being transported to the plasma membrane, it failed to induce cell-cell fusion. We assessed both vaccine candidates in prime-boost regimens in the susceptible transgenic K18-human angiotensin-converting enzyme 2 (K18-hACE2) in mice and in golden Syrian hamsters. Robust immunity and protection from disease was induced with either vaccine in both animal models. Remarkably, the MVA-Spf vaccine candidate produced higher levels of antibodies, a stronger T cell response, and a higher degree of protection from challenge. In addition, the level of SARS-CoV-2 in the brain of MVA-Spf inoculated mice was decreased to undetectable levels. Those results add to our current experience and range of vaccine vectors and technologies for developing a safe and effective COVID-19 vaccine.
مصطلحات الفهرس: COVID-19, SARS-CoV-2, Immunization, Modified vaccinia virus Ankara, Poxvirus, Recombinant viral vectors, Vaccine, artículo
URL: http://hdl.handle.net/10261/331347Test
https://api.elsevier.com/content/abstract/scopus_id/85160305767Test
https://doi.org/10.3390/vaccines11051006Test
Centro de Investigación en Sanidad Animal (CISA)
Publisher's version
https://doi.org/10.3390/vaccines11051006Test
Sí
info:eu-repo/grantAgreement/AEI//PID2021-128466OR-I00
الإتاحة: Open access content. Open access content
https://creativecommons.org/licenses/by/4.0Test
openAccess
ملاحظة: English
أرقام أخرى: CTK oai:digital.csic.es:10261/331347
Vaccines 11(5): e1006 (2023)
10.3390/vaccines11051006
2076-393X
37243110
2-s2.0-85160305767
1395213299
المصدر المساهم: CSIC
From OAIster®, provided by the OCLC Cooperative.
رقم الانضمام: edsoai.on1395213299
قاعدة البيانات: OAIster