Enhanced Synthetic pDNA Vaccines against SARS-CoV-2

Publication ID: 24-11857621_0006_PTD
Published: October 28, 2025
Category:Direct Improvements & Enhancements

Legal Citation

pr1or.art Inc., “Enhanced Synthetic pDNA Vaccines against SARS-CoV-2,” Published Technical Disclosure No. 24-11857621_0006_PTD, Published October 28, 2025, available at https://archive.pr1or.art/24-11857621_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. 11,857,621.

Summary of the Inventive Concept

The present inventive concept relates to direct improvements and enhancements of synthetic pDNA vaccines against SARS-CoV-2, providing enhanced immunogenicity, stability, and efficacy.

Background and Problem Solved

The original patent, 'Synthetic pDNA vaccines against COVID-19', introduced a stable, engineered plasmid-based vaccine. However, the existing vaccine had limitations in terms of receptor binding domain degradation and immunogenicity. The present inventive concept addresses these limitations by introducing modified S proteins with enhanced receptor binding domains, optimized epitopes, and co-administered adjuvants to enhance immunogenicity.

Detailed Description of the Inventive Concept

The inventive concept comprises a system for inducing immune responses against SARS-CoV-2, featuring a pDNA vaccine encoding a modified S protein with an enhanced receptor binding domain, stabilized by a specific motif to reduce degradation. Additionally, the inventive concept includes a method for preventing or treating SARS-CoV-2 infection by administering a pDNA vaccine encoding a SARS-CoV-2 S protein epitope with improved immunogenicity, optimized for enhanced humoral and cellular responses. The pDNA vaccine is formulated with a plasmid vector encoding a S protein variant with enhanced stability and immunogenicity, comprising a deletion of at least 5 amino acids in the S1 subunit. Furthermore, the inventive concept includes a method for enhancing the efficacy of the pDNA vaccine by co-administering an adjuvant that targets the TLR9 receptor, formulated to enhance the immunogenicity of the S protein epitope. The inventive concept also features a system for rapid production of pDNA vaccines against SARS-CoV-2, comprising a plasmid vector encoding a S protein variant with optimized codon usage for enhanced expression, and a microfluidic device for high-throughput production of the pDNA vaccine.

Novelty and Inventive Step

The inventive concept's novelty lies in the introduction of modified S proteins with enhanced receptor binding domains, optimized epitopes, and co-administered adjuvants, which provide a significant improvement over the original patent. The inventive step is the combination of these elements, which results in a more effective and efficient pDNA vaccine against SARS-CoV-2.

Alternative Embodiments and Variations

Alternative embodiments of the inventive concept could include the use of different adjuvants, varying the deletion of amino acids in the S1 subunit, or incorporating additional epitopes to enhance immunogenicity. Variations could also include the use of different plasmid vectors, microfluidic devices, or production methods to enhance the efficiency and scalability of the pDNA vaccine production.

Potential Commercial Applications and Market

The enhanced synthetic pDNA vaccines against SARS-CoV-2 have significant commercial potential in the vaccine market, particularly in the context of the ongoing COVID-19 pandemic. The inventive concept could be applied in various industries, including pharmaceuticals, biotechnology, and healthcare, and could be used to develop vaccines against other diseases as well.

CPC Classifications

SectionClassGroup
A A61 A61K39/215
A A61 A61K9/0019
A A61 A61P31/14
C C07 C07K14/005
A A61 A61K2039/53
A A61 A61K2039/54
A A61 A61K2039/545
C C12 C12N2770/20022
C C12 C12N2770/20034
C C12 C12N2770/20071

Field of Art

Molecular Biology and Vaccine Development, specifically focused on DNA vaccine design for viral pathogens, with expertise in plasmid engineering, protein modification, and immunological optimization

Person of Ordinary Skill (PHOSITA) Profile

A skilled researcher with advanced degrees in molecular biology or immunology, experienced in genetic engineering techniques, vaccine design, protein epitope optimization, and understanding of viral protein structures and immune responses

Obviousness Rationale

A person of ordinary skill would recognize that the PTD's modifications to the SARS-CoV-2 vaccine represent predictable variations within the established vaccine design paradigm. The proposed enhancements, such as S protein domain modifications, epitope optimization, and adjuvant strategies, are logical extensions of known vaccine development approaches. These variations would be considered routine engineering choices for improving vaccine efficacy and immunogenicity.

Obvious Combinations & Variations

Source Patent Element
Original plasmid DNA vaccine encoding SARS-CoV-2 spike protein sequences
PTD Variation
Modified S protein with deletion of at least 5 amino acids in S1 subunit to enhance stability and immunogenicity
Obviousness Reasoning
Routine protein engineering technique to modify antigen structure for improved immune response, representing a predictable optimization strategy known in vaccine development
Source Patent Element
Base plasmid vector encoding viral protein
PTD Variation
Plasmid vector with optimized codon usage for enhanced protein expression
Obviousness Reasoning
Well-established genetic engineering approach to improve protein production, representing a known technique for enhancing vaccine antigen expression
Source Patent Element
Initial pDNA vaccine design targeting SARS-CoV-2
PTD Variation
Co-administration with TLR9 receptor-targeting adjuvant to enhance immunogenicity
Obviousness Reasoning
Standard immunological strategy of using adjuvants to modulate and enhance immune responses, representing a predictable method of vaccine improvement
Source Patent Element
Basic plasmid DNA vaccine production method
PTD Variation
Incorporation of microfluidic device for high-throughput vaccine production
Obviousness Reasoning
Obvious technological upgrade using known microfluidic technologies to improve manufacturing scalability and efficiency
Source Patent Element
Original spike protein epitope design
PTD Variation
Enhanced receptor binding domain stabilized by specific motif to reduce degradation
Obviousness Reasoning
Predictable protein engineering approach to improve antigen stability, representing a standard technique for enhancing vaccine performance
35 U.S.C. § 103 Summary: Pursuant to 35 U.S.C. ยง 103, the variations disclosed in the published technical disclosure (PTD) would have been obvious to a person having ordinary skill in the art at the time of invention, when viewed in light of US Patent 11857621. The proposed modifications represent routine engineering choices within the established paradigm of DNA vaccine design, involving predictable optimizations of protein structure, expression, and immunological performance that would be apparent to a skilled practitioner in the field of molecular vaccine development.

Original Patent Information

Patent NumberUS 11,857,621
TitleSynthetic pDNA vaccines against COVID-19
Assignee(s)Imam Abdulrahman Bin Faisal University