Allogeneic T-Cell Induction of Endogenous IL-12

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Current immunotherapy methods face challenges in effectively promoting IL-12 production in patients, particularly those with cancer, due to toxicity issues associated with exogenous IL-12 administration and tumor inhibition of IL-12 expression.

Innovation Solution

Administering allogeneic activated T-cells to patients, which induce the production of endogenous IL-12 by the patient's antigen-presenting cells, using various routes such as intradermal, intravenous, or intralesional, to achieve detectable and sustained levels of IL-12 in plasma without significant toxicity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Quantity of substance

If exogenous IL-12 is administered to patients, then IL-12 levels increase, but toxicity increases significantly

Engineering Contradiction:
ImproveIL-12 levelsVSAvoidtoxicity
Core Design Contradiction:
Quantity of substanceVSObject-affected harmful factors

Solution Approach 1:

The patent employs the patient's own antigen-presenting cells to produce endogenous IL-12 internally, rather than administering exogenous IL-12. This self-service approach allows the body to generate the required cytokine levels through its own biological mechanisms, avoiding the toxicity associated with external administration while maintaining therapeutic efficacy

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The patent uses antigen-presenting cells as an intermediary between the administered composition and IL-12 production. These cells process the administered material and convert it into endogenous IL-12 through natural biological processes, serving as a mediator that transforms the input into the desired therapeutic output without direct toxic exposure

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If immunotherapy is used to promote IL-12 production, then anti-tumor immunity is enhanced, but tumor inhibition of IL-12 expression persists

Engineering Contradiction:
Improveanti-tumor immunityVSAvoidtumor inhibition of IL-12 expression
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent administers a composition containing antigens and adjuvants before attempting to stimulate IL-12 production. This preliminary action prepares the antigen-presenting cells and creates a favorable immunological environment that overcomes the tumor's suppressive effects, enabling subsequent successful IL-12 induction

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The patent employs adjuvants in the administered composition that counteract the tumor's inhibitory effects on IL-12 expression. These adjuvants create a preliminary opposing force against the tumor's suppression mechanisms, neutralizing the harmful inhibition before it can block IL-12 production

Inventive Principle:
Principle #9Preliminary anti-action

3Quantity of substance

If allogeneic activated T-cells are administered, then endogenous IL-12 production is induced, but treatment complexity increases

Engineering Contradiction:
Improveendogenous IL-12 productionVSAvoidtreatment complexity
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The patent uses allogeneic activated T-cells that can serve multiple functions: they act as antigen-presenting cells, produce cytokines, and stimulate endogenous IL-12 production. This multi-functionality reduces the need for separate treatment components, simplifying the overall treatment approach despite the sophisticated biological mechanisms involved

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

Data Source

PatentUS11883490B2Induction of IL-12 using immunotherapy
Publication Date: 2024.01.30 MIRROR BIOLOGICS INC
  • US11883490B2 patent drawing

AI summary

The present invention relates to compositions and methods that promote the induction of IL-12 in a patient. The composition includes activated allogeneic cells that are administered to a patient with a disease such as cancer. Administration of the composition skews the patient's immune response to a Th1 environment and produces detectable levels of IL-12 in the patient's plasma, without any IL-12 related toxicity.