CPI, Caltech, University of Oxford, Ingenza - Broadly Protective Coronavirus Vaccine

  • Funded by Coalition for Epidemic Preparedness Innovations (CEPI)
  • Total publications:1000 publications

Grant number: N/A

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Key facts

  • Disease

    COVID-19
  • start year

    2022
  • Known Financial Commitments (USD)

    $30,000,000
  • Funder

    Coalition for Epidemic Preparedness Innovations (CEPI)
  • Principal Investigator

    N/A

  • Research Location

    United Kingdom, United States of America
  • Lead Research Institution

    CPI, Caltech, University of Oxford, Ingenza
  • Research Priority Alignment

    N/A
  • Research Category

    Vaccines research, development and implementation

  • Research Subcategory

    Pre-clinical studies

  • Special Interest Tags

    N/A

  • Study Type

    Clinical

  • Clinical Trial Details

    Clinical Trial, Phase I

  • Broad Policy Alignment

    Pending

  • Age Group

    Unspecified

  • Vulnerable Population

    Unspecified

  • Occupations of Interest

    Unspecified

Abstract

Up to $30m funding will be provided to advance an innovative vaccine technology that could protect against current and future SARS-CoV-2 variants and other SARS-like Betacoronaviruses. New peer-reviewed research, out today in Science, demonstrates the vaccine platform provides protection against a spectrum of SARS-like Betacoronaviruses in preclinical models. This is the eleventh award to be made by CEPI as part of its broadly protective coronavirus vaccine programme, making the coalition a global leader in all-in-one coronavirus vaccine research. Jul 5, 2022 'Äî The Coalition for Epidemic Preparedness Innovations (CEPI) has partnered with a consortium of research and technological institutions to develop a novel vaccine to provide protection against COVID-19 caused by current and future SARS-CoV-2 variants, as well as to protect against other SARS-like Betacoronaviruses*. The project will be led in manufacturing efforts by UK-based deep tech innovation organisation CPI to advance the novel vaccine developed at Caltech and The University of Oxford, and manufactured using microbes engineered by industrial biotechnology leader, Ingenza Ltd. CEPI will provide up to US $30 million to support the development of the vaccine through Phase I trials, including preclinical work, with the aim to establish first-in-human clinical proof of concept for the vaccine. The funding will also support the design of the vaccine and regulatory activities. Recognising the risk of future coronavirus threats, CEPI has established itself as the global leader in funding all-in-one coronavirus vaccine research. This is the eleventh award to be made as part of CEPI's US $200 million programme supporting projects that could provide broad protection against SARS-CoV-2 variants and other Betacoronaviruses. CEPI also today announced another broadly protective coronavirus vaccine partnership with Codiak Biosciences. The programme is a central part of CEPI's innovative US $3.5 billion pandemic preparedness plan that seeks to reduce, or even eliminate, the threat of future pandemics. An innovative coronavirus-fighting technology Many COVID-19 vaccine candidates work by presenting fragments of the SARS-CoV-2 spike protein (known as the receptor-binding domain, or RBD) to the body to generate an immune response. However, newly arising SARS-CoV-2 variants, such as various forms of Omicron, are increasingly able to evade the original vaccine's immune response. Changeable regions of their RBDs have been mutated in ways that allow them to escape from the original immune response. By contrast, this new vaccine aims to create immunity to known and future strains simultaneously is designed to focus the immune response on parts of RBD shared by all viruses in the SARS-like Betacoronavirus family, including future variants. It does this by presenting spike protein fragment RBDs from SARS-CoV-2 together with RBDs from seven other different types of coronaviruses on protein nanoparticles termed "mosaic-8" nanoparticles. These coronavirus RBDs are attached to a nanoparticle by protein tags, enabling the structure to display fragments from multiple viruses on a single nanoparticle. The nanoparticle contains a protein "glue" on its surface that attaches to engineered coronavirus fragments like 'Äòvelcro,' an innovative approach to permanently link proteins to each other. Supporting this approach, new research published today in Science, demonstrates that this mosaic-8 nanoparticle vaccine technology elicits protective immune responses in preclinical models against SARS-like Betacoronaviruses with components displayed on the mosaic nanoparticle as well as coronaviruses from which no components were displayed. This included SARS-like Betacoronaviruses seen in animals with the potential to spillover to humans. These findings suggest that the technology may also provide protection against future novel SARS-CoV-2 variants and as-yet-undiscovered coronaviruses that could transfer into the human population in the future.

Publicationslinked via Europe PMC

The Skills to Manage Pain Randomized Trial: Results of Antiretroviral Therapy Adherence, HIV Primary Care Retention, and Virologic Suppression Outcomes.

A reanalysis of population dynamics in the Casas Grandes region of Northern Mexico using mitochondrial DNA.

Action painting under spectroscopic light: Excited-state exchange interactions behind the vibrant blue in Jackson Pollock's <i>Number 1A, 1948</i>.

Improving the efficacy of anti-SSEA4 antibody in pancreatic cancer immunotherapy with glyco-optimization and immune checkpoint blockade.

Clenbuterol induces lean mass and muscle protein accretion, but attenuates cardiorespiratory fitness and desensitizes muscle β<sub>2</sub>-adrenergic signalling.

Posttranscriptional control of the B cell receptor by HuR is essential for innate B cell maintenance and function.

Five-year results of the SCENT trial with Surpass flow diverters to treat large or giant wide-neck aneurysms.

Peritumoral macrophages recruit eosinophils to promote antitumor immune responses in breast cancer.

Intention judgments are not a reliable measure of intuitive preferences.