Enhanced Recombinant Measles Virus-Based Zika Vaccine

Publication ID: 24-11857616_0006_PTD
Published: October 28, 2025
Category:Direct Improvements & Enhancements

Legal Citation

pr1or.art Inc., “Enhanced Recombinant Measles Virus-Based Zika Vaccine,” Published Technical Disclosure No. 24-11857616_0006_PTD, Published October 28, 2025, available at https://archive.pr1or.art/24-11857616_0006_PTD
This technical disclosure describes improvements that would be readily apparent to a Person Having Ordinary Skill In The Art (PHOSITA) when considered in combination with the foundational architecture disclosed in U.S. Patent No. 11,857,616.

Summary of the Inventive Concept

The inventive concept discloses improvements to the recombinant measles virus expressing Zika virus prM and E proteins, enhancing its safety, efficacy, and immunogenicity.

Background and Problem Solved

The original patent's recombinant measles virus-based Zika vaccine has limitations related to antibody-dependent enhancement and inadequate immunogenicity. The new inventive concept addresses these limitations by modifying the E protein to reduce its binding affinity to target cells, inactivating the expressed E protein to prevent fusion, and enhancing the stability and efficacy of the vaccine through nanoparticle-based delivery.

Detailed Description of the Inventive Concept

The inventive concept comprises five direct improvements and enhancements to the original patent's recombinant measles virus-based Zika vaccine. Firstly, the E protein is modified to have a reduced binding affinity to target cells, reducing the risk of antibody-dependent enhancement. Secondly, a method for producing a vaccine candidate involves expressing the recombinant measles virus in a mammalian cell line and inactivating the expressed E protein to prevent fusion with target cells. Thirdly, a nanoparticle-based delivery vehicle is used to enhance the stability and efficacy of the vaccine. Fourthly, the prM protein is modified to have an increased half-life, enhancing the immunogenicity of the vaccine. Finally, co-administering the vaccine candidate with an adjuvant that stimulates a Th1-type immune response further enhances its immunogenicity.

Novelty and Inventive Step

The new claims introduce non-obvious modifications to the original patent's recombinant measles virus-based Zika vaccine, including the reduced binding affinity of the E protein, inactivation of the expressed E protein, nanoparticle-based delivery, modified prM protein, and co-administration with a Th1-type immune response-stimulating adjuvant.

Alternative Embodiments and Variations

Alternative embodiments of the inventive concept may include using different nanoparticle materials or adjuvants, varying the dosage or administration route of the vaccine, or combining the recombinant measles virus with other Zika virus antigens.

Potential Commercial Applications and Market

The enhanced recombinant measles virus-based Zika vaccine has significant commercial potential in the vaccine market, particularly in regions where Zika virus is prevalent. The inventive concept's improved safety, efficacy, and immunogenicity make it an attractive solution for governments, healthcare organizations, and pharmaceutical companies.

CPC Classifications

SectionClassGroup
A A61 A61K39/12
C C07 C07K14/005
C C12 C12N7/00
A A61 A61K2039/5254
A A61 A61K2039/53
C C12 C12N2760/18421
C C12 C12N2760/18423
C C12 C12N2770/24122
C C12 C12N2770/24123
C C12 C12N2770/24134

Field of Art

Virology, vaccine development, recombinant viral vector technologies, with specific expertise in measles virus-based vaccine platforms and genetic engineering of viral proteins

Person of Ordinary Skill (PHOSITA) Profile

A skilled researcher with advanced degrees in virology or molecular biology, experienced in recombinant virus design, protein modification techniques, and vaccine development, familiar with genetic manipulation of viral vectors and immunological engineering strategies

Obviousness Rationale

A person skilled in the art would recognize that the proposed modifications to the measles virus-based Zika vaccine represent predictable variations within established vaccine engineering approaches. The disclosed enhancements leverage known techniques for improving viral vector vaccines, including protein modification, delivery optimization, and immunogenicity enhancement. These modifications follow standard methodological approaches in vaccine design that would be apparent to a skilled practitioner seeking to improve the original viral vector vaccine platform.

Obvious Combinations & Variations

Source Patent Element
Recombinant measles virus expressing Zika virus prM and E proteins
PTD Variation
Modifying E protein to reduce binding affinity to target cells
Obviousness Reasoning
Reducing viral protein binding is a standard technique to mitigate potential adverse immune responses, representing a predictable design optimization known in vaccine development
Source Patent Element
Nucleic acid construct encoding viral proteins
PTD Variation
Nanoparticle-based delivery vehicle for enhanced vaccine stability
Obviousness Reasoning
Nanoparticle delivery is a well-established method for improving vaccine pharmacokinetics and stability, representing a known technological solution for vaccine formulation challenges
Source Patent Element
Measles virus vaccine strain
PTD Variation
Co-administration with Th1-type immune response-stimulating adjuvant
Obviousness Reasoning
Adjuvant selection to modulate immune response is a routine strategy in vaccine design, with predictable methods for enhancing immunological outcomes
Source Patent Element
Polynucleotide encoding viral proteins
PTD Variation
Inactivating expressed E protein to prevent cellular fusion
Obviousness Reasoning
Protein inactivation techniques are standard molecular biology methods for controlling viral vector behavior, representing a predictable engineering approach
Source Patent Element
Zika virus protein encoding sequences
PTD Variation
Modifying prM protein to increase half-life
Obviousness Reasoning
Protein modification to enhance stability is a common protein engineering technique with well-understood methodological approaches
35 U.S.C. § 103 Summary: Based on the teachings of US Patent 11857616 and the disclosed technical variations, a person having ordinary skill in the art would find the proposed vaccine modifications obvious and predictable extensions of existing recombinant viral vector technologies. The systematic enhancements to protein binding, delivery mechanisms, and immunological properties represent routine engineering approaches that would be apparent to a skilled practitioner seeking to optimize a measles virus-based Zika vaccine platform.

Original Patent Information

Patent NumberUS 11,857,616
TitleRecombinant measles virus expressing zika virus prM and E proteins
Assignee(s)CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS), Institut Pasteur