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.

Virology
|March 11, 2014
PubMed

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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