Tumor Immunotherapy Composition Using Microbial Innate Immune Activation

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Solution Overview

Problem

Current cancer treatments, including surgery, radiotherapy, chemotherapy, targeted therapy, and passive immunotherapy, fail to systematically address tumor metastasis and restore immune surveillance mechanisms, with T-cell-based immunotherapies showing limited efficacy and significant toxic side effects.

Innovation Solution

A pharmaceutical composition comprising microbial agents like Staphylococcus aureus, Bordetella pertussis, diphtheria toxoid, tetanus toxoid, Salmonella typhi, and Salmonella paratyphi, combined with polyinosinic acid, polycytidylic acid, and vitamin, stimulates the innate immune system to activate adaptive immunity, enhancing tumor-specific responses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If T cell-based immunotherapy is used, then adaptive immune response is stimulated, but response rate remains low and toxic side effects occur

Engineering Contradiction:
Improveresponse rateVSAvoidtoxic side effects
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The patent segments the immune system into innate and adaptive components, using innate immune stimulants (cyclic ADP-ribse, bacterial products) as a separate first line of action that activates adaptive immunity indirectly, thereby avoiding the direct toxicities of T cell-based therapies while maintaining effective tumor response

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The patent introduces innate immune stimulants as intermediary substances that bridge the gap between tumor treatment and adaptive immune activation. These intermediaries (cyclic ADP-ribse, bacterial cell wall products) activate macrophages and dendritic cells, which then stimulate T cell responses without requiring direct T cell targeting, thus avoiding the toxicities associated with T cell-based immunotherapies

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If chemotherapy is used, then cancer cells are killed effectively, but normal cells are damaged and immune system is impaired

Engineering Contradiction:
Improvecancer cell killing efficacyVSAvoiddamage to normal cells and immune system
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The patent converts the harmful non-selective killing mechanism of chemotherapy into a beneficial selective immune activation mechanism. Instead of directly killing cancer cells (which damages normal cells), the therapy uses innate immune stimulants to activate the body's own immune surveillance mechanisms, turning the harm of non-selective toxicity into the benefit of selective immune-mediated cancer elimination

Inventive Principle:
Principle #22Blessing in disguise (Convert harm into benefit)

Solution Approach 2:

The patent enables the immune system to perform self-service by using innate immune stimulants that activate endogenous immune cells (macrophages, dendritic cells, T cells) to recognize and eliminate cancer cells. This self-service mechanism eliminates the need for external cytotoxic agents that damage normal cells, as the body's own immune system performs the cancer-killing function selectively

Inventive Principle:
Principle #25Self-service

3Reliability

If surgery and radiotherapy are used, then localized lesions are eliminated, but disseminated disease cannot be eradicated

Engineering Contradiction:
Improvelocal lesion eliminationVSAvoidability to address disseminated disease
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent creates a universal therapy that can address both localized and disseminated cancer through the activation of systemic immune surveillance. The innate immune stimulants trigger a systemic immune response that can detect and eliminate cancer cells anywhere in the body, making the therapy universally applicable to various cancer stages and locations, unlike surgery and radiotherapy that are limited to localized treatment

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

4Reliability

If targeted therapy is used, then specificity is improved, but scope of action is limited and drug resistance remains

Engineering Contradiction:
ImprovespecificityVSAvoidscope of action
Core Design Contradiction:
ReliabilityVSAdaptability or versatility

Solution Approach 1:

The patent introduces dynamic adaptability through innate immune stimulants that can activate different immune cell types and signaling pathways based on the tumor's characteristics. This dynamic immune activation allows the therapy to adapt to various tumor types and stages, overcoming the fixed specificity of targeted therapies and addressing drug resistance by continuously evolving the immune response

Inventive Principle:
Principle #15Dynamics

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The composition effectively activates the immune system to target cancer cells with minimal side effects, reducing treatment costs and improving treatment outcomes for various cancers, including solid tumors, while being broadly applicable and safe.

Implementation Method 1

stimulates the innate immune system to activate adaptive immunity, enhancing tumor-specific responses

Methodology Applied
Scientific EffectImmune stimulation:

Data Source

PatentUS20260048111A1Pharmaceutical Composition, Preparation Method and Use Thereof
Publication Date: 2026.02.19 PUGONG BIOTECH (HANGZHOU) CO LTD
  • US20260048111A1 patent drawing
  • US20260048111A1 patent drawing
  • US20260048111A1 patent drawing

AI summary

The present disclosure relates to the technical field of medicine, and in particular to a pharmaceutical composition, preparation method and use thereof. The pharmaceutical composition includes a first active ingredient, a second active ingredient, and a pharmaceutically acceptable carrier or excipient. The first active ingredient is a microbial agent, including one or more of Staphylococcus aureus, Bordetella pertussis, diphtheria toxoid, tetanus toxoid, Salmonella typhi, and Salmonella paratyphi. The second active ingredient includes polyinosinic acid, polycytidylic acid, and vitamin. The pharmaceutical composition of the present disclosure pertains to an artificial active immunotherapy for tumors. It can “stimulate” the entire immune system, making the therapy of using bacteria to activate the human immune system to kill cancer cells highly stable and reliable. This composition can significantly save and prolong the lives of cancer patients while exhibiting extremely high safety, minimal toxic side effects, and low production costs.