Immunogenic Peptides Inducing CD8+ T Cell Immunity Against HSV

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Solution Overview

Problem

Current treatments for Herpes Simplex Virus (HSV) infections are palliative and do not provide a cure, with many infected individuals being asymptomatic and unknowingly shedding the virus, leading to a need for effective inhibition and treatment methods.

Innovation Solution

Development of immunogenic peptides with specific amino acid sequences, such as NLLTTPKFT and RMLGDVMAV, formulated in compositions that induce CD8+ T cell-dependent protective immunity against HSV-1 and HSV-2 infections, using adjuvants like CpG1826 and lipid-tailed peptides, and incorporating epitopes from HSV-1 gB, gD, or other proteins.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If palliative treatments like acyclovir are used, then HSV infection symptoms are managed, but the infection cannot be cured and virus shedding continues

Engineering Contradiction:
Improvetreatment effectivenessVSAvoidvirus shedding
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent applies preliminary action by administering immunogenic peptides containing HSV-specific epitopes before or during viral infection to proactively stimulate the immune system. This preventive immunization approach enables the host to develop CD8+ T cell responses in advance, allowing for more effective control of viral replication and shedding when infection occurs, rather than merely managing symptoms after infection is established

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent uses immunogenic peptides as intermediaries to bridge the gap between the host immune system and the HSV virus. These peptides, containing specific epitopes from HSV proteins (such as gB, gD, and UL49.5), act as mediators that stimulate the immune system to recognize and respond to the virus, thereby enhancing the body's natural defense mechanisms without directly interacting with the virus itself

Inventive Principle:
Principle #24Intermediary (Mediator)

2Object-generated harmful factors

If asymptomatic individuals are not identified, then they unknowingly shed virus, but screening and identification methods are complex

Engineering Contradiction:
Improveunrecognized virus sheddingVSAvoidscreening complexity
Core Design Contradiction:
Object-generated harmful factorsVSDevice complexity

Solution Approach 1:

The patent extracts specific immunogenic epitopes from complex HSV proteins to create simplified peptide compositions. By isolating and using only the critical epitopic regions (such as those from gB, gD, and UL49.5 proteins) that are recognized by protective T cell responses, the patent creates a streamlined diagnostic and therapeutic approach that avoids the complexity of analyzing entire viral proteins or using complex screening protocols

Inventive Principle:
Principle #2Taking out (Extraction)

Solution Approach 2:

The patent applies universality by designing immunogenic peptides that can serve multiple functions: they can be used for both therapeutic vaccination to prevent infection and for diagnostic purposes to identify infected individuals. The peptides containing conserved epitopes from HSV-1 and HSV-2 can universally target both virus types, enabling a single intervention strategy to address diverse clinical scenarios including asymptomatic detection

Inventive Principle:
Principle #6Universality (Multi-functionality)

Data Source

PatentUS9878033B2Immunogenic peptides for treatment of herpes simplex virus infection and conditions
Publication Date: 2018.01.30 RGT UNIV OF CALIFORNIA
  • US9878033B2 patent drawing
  • US9878033B2 patent drawing
  • US9878033B2 patent drawing

AI summary

Certain embodiments of the present invention provide immunogenic compositions that comprise one or more peptides having an amino acid sequence selected from the group consisting of NLLTTPKFT and RMLGDVMAV and methods for administering such compositions to a mammal and thereby inducing in the mammal a CD8+ T cell-dependent protective immunity against an HSV-1 infection, an HSV-2 infection, an HSV-1 condition, an HSV-2 condition, or combinations thereof.