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Updated: May 2, 2026

Protocol for Recombinant RBD-based SARS Vaccines: Protein Preparation, Animal Vaccination and Neutralization Detection
Published on: May 2, 2011
Protection from SARS coronavirus conferred by live measles vaccine expressing the spike glycoprotein
Nicolas Escriou1, Benoît Callendret1, Valérie Lorin1
1Institut Pasteur, Unité de Génétique Moléculaire des Virus à ARN, Département de Virologie, F-75015 Paris, France; CNRS, UMR 3569, F-75015 Paris, France; Univ. Paris Diderot, Sorbonne, Paris Cité, EA 302, F-75015 Paris, France.
Abstract:
The recent identification of a novel human coronavirus responsible of a SARS-like illness in the Middle-East a decade after the SARS pandemic, demonstrates that reemergence of a SARS-like coronavirus from an animal reservoir remains a credible threat. Because SARS is contracted by aerosolized contamination of the respiratory tract, a vaccine inducing mucosal long-term protection would be an asset to control new epidemics. To this aim, we generated live attenuated recombinant measles vaccine (MV) candidates expressing either the membrane-anchored SARS-CoV spike (S) protein or its secreted soluble ectodomain (Ssol). In mice susceptible to measles virus, recombinant MV expressing the anchored full-length S induced the highest titers of neutralizing antibodies and fully protected immunized animals from intranasal infectious challenge with SARS-CoV. As compared to immunization with adjuvanted recombinant Ssol protein, recombinant MV induced stronger and Th1-biased responses, a hallmark of live attenuated viruses and a highly desirable feature for an antiviral vaccine.
Insights
A novel measles vaccine candidate expressing SARS-CoV spike protein shows promise for controlling future epidemics. This live attenuated vaccine fully protected mice against SARS-CoV challenge, offering a potential mucosal immunity strategy.
Area of Science:
- Virology
- Vaccinology
- Immunology
Background:
- Reemergence of SARS-like coronaviruses poses a significant public health threat.
- Effective vaccines are needed to prevent transmission, particularly via aerosolized respiratory routes.
Purpose of the Study:
- To develop a live attenuated vaccine candidate for SARS-CoV using a measles virus (MV) vector.
- To evaluate the immunogenicity and protective efficacy of MV-based vaccines expressing SARS-CoV spike (S) protein.
Main Methods:
- Generation of recombinant measles virus (MV) candidates expressing either membrane-anchored full-length SARS-CoV spike (S) protein or its soluble ectodomain (Ssol).
- Immunization of mice susceptible to measles virus with recombinant MV candidates.
- Assessment of neutralizing antibody titers and protection against intranasal SARS-CoV challenge.
Main Results:
- Recombinant MV expressing the anchored full-length S protein induced the highest neutralizing antibody titers.
- Immunization with this candidate fully protected mice from SARS-CoV challenge.
- Compared to adjuvanted protein, MV induced stronger, Th1-biased immune responses.
Conclusions:
- Live attenuated measles virus vectors are effective for delivering SARS-CoV antigens.
- MV-based vaccines expressing SARS-CoV S protein can induce protective immunity and Th1-biased responses, desirable for antiviral vaccines.
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