CureVac's Second-Generation mRNA COVID-19 Vaccine Candidate Shows Promise

  • Author: ChemistryViews
  • Published: 18 August 2021
  • Copyright: Wiley-VCH GmbH
thumbnail image: CureVac's Second-Generation mRNA COVID-19 Vaccine Candidate Shows Promise

CureVac and GSK have published preclinical data evaluating the immune responses and protective efficacy of CureVac's first-generation vaccine candidate, CVnCoV, and the second-generation vaccine candidate, CV2CoV, against SARS-CoV-2 in non-human primates. The team studied eighteen cynomolgus macaques that were vaccinated with two doses of 12 ug of lipid nanoparticle formulated CVnCoV, CV2CoV, or sham (N = 6/group).

CV2CoV induced substantially higher binding and neutralizing antibodies, memory B cell responses, and T cell responses as compared with CVnCoV. CV2CoV also induced more potent neutralizing antibody responses against SARS-CoV-2 variants, including B.1.351 (beta), B.1.617.2 (delta), and C.37 (lambda). While CVnCoV provided partial protection against SARS-CoV-2 challenge, CV2CoV afforded robust protection with markedly lower viral loads in the upper and lower respiratory tract. Antibody responses correlated with protective efficacy.

The researchers say the optimized mRNA backbone used in this work has the potential for a multivalent or combined approach to address multiple emerging variants in one vaccine. Following the current preclinical development of CV2CoV, a Phase 1 clinical trial is expected to start in the fourth quarter of 2021.

The vaccine candidate, CV2CoV, is a non-chemically modified mRNA encoding the full-length prefusion-stabilized spike protein of the SARS-CoV-2 virus and formulated within lipid nanoparticles. CV2CoV was engineered with specifically optimized non-coding regions to enable enhanced mRNA translation for increased and prolonged protein expression compared to the first-generation mRNA backbone.


  • CureVac AG, Tübingen, GermanyOptimization of Non-Coding Regions Improves Protective Efficacy of an mRNA SARS-CoV-2 Vaccine in Nonhuman Primates,
  • Optimization of Non-Coding Regions Improves Protective Efficacy of an mRNA SARS-CoV-2 Vaccine in Nonhuman Primates,
    Makda S. Gebre, Susanne Rauch, Nicole Roth, Jingyou Yu, Abishek Chandrashekar, Noe B. Mercado, Xuan He, Jinyan Liu, Katherine McMahan, Amanda Martinot, Tori Giffin, David Hope, Shivani Patel, Daniel Sellers, Owen Sanborn, Julia Barrett, Xiaowen Liu, Andrew C. Cole, Laurent Pessaint, Daniel Valentin, Zack Flinchbaugh, Jake Yalley-Ogunro, Jeanne Muench, Renita Brown, Anthony Cook, Elyse Teow, Hanne Andersen, Mark G. Lewis, Stefan O. Mueller, Benjamin Petsch, Dan H. Barouch,
    bioRxiv 2021.
    https://doi.org/10.1101/2021.08.13.456316


    The research has been published as a preprint and has not yet been peer-reviewed.

Also of Interest

 

 

 



 

Article Views: 3682

Sign in Area

Please sign in below

Additional Sign In options

Please note that to comment on an article you must be registered and logged in.
Registration is for free, you may already be registered to receive, e.g., the newsletter. When you register on this website, please ensure you view our terms and conditions. All comments are subject to moderation.

Article Comments - To add a comment please sign in

If you would like to reuse any content, in print or online, from ChemistryViews.org, please contact us first for permission and consult our permission guidance prior to making your request

Follow on Facebook Follow on Twitter Follow on YouTube Follow on LinkedIn Follow on Instagram RSS Sign up for newsletters

Magazine of Chemistry Europe (16 European Chemical Societies) published by Wiley-VCH