Enhanced CAR-T Cell Therapy through Synergistic Combinations

Publication ID: 24-11857574_0008_PTD
Published: October 28, 2025
Category:Synergistic Combinations

Legal Citation

pr1or.art Inc., “Enhanced CAR-T Cell Therapy through Synergistic Combinations,” Published Technical Disclosure No. 24-11857574_0008_PTD, Published October 28, 2025, available at https://archive.pr1or.art/24-11857574_0008_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. 11,857,574.

Summary of the Inventive Concept

A novel system integrating genetically engineered T cells with disrupted Regnase-1 and/or TGFBRII genes with distinct technologies like AI, IoT, blockchain, and new materials, enhancing CAR-T cell therapy through improved monitoring, control, and personalized treatment.

Background and Problem Solved

Chimeric antigen receptor (CAR) T-cell therapy, despite its promise, faces limitations in terms of T cell growth, persistence, and personalized treatment. The original patent addresses some of these limitations by genetically engineering T cells with disrupted Regnase-1 and/or TGFBRII genes. However, further improvements can be achieved by integrating these engineered T cells with other technologies to create a more powerful and efficient system.

Detailed Description of the Inventive Concept

The new inventive concept combines the genetically engineered T cells with disrupted Regnase-1 and/or TGFBRII genes from the original patent with four distinct technologies: AI-powered analytics for real-time monitoring of T cell growth and persistence, blockchain technology for secure storage and management of patient-specific treatment data, nanomaterials for enhanced T cell expansion and viability, and IoT-enabled bioreactors for real-time monitoring and control of T cell culture conditions. This synergistic combination enables improved CAR-T cell therapy through enhanced monitoring, control, and personalized treatment.

Novelty and Inventive Step

The new claims introduce a novel combination of genetically engineered T cells with disrupted Regnase-1 and/or TGFBRII genes and distinct technologies, which is not obvious from the original patent. The inventive step lies in the integration of these components to create a more powerful and efficient system for CAR-T cell therapy.

Alternative Embodiments and Variations

Alternative embodiments may include integrating the genetically engineered T cells with other AI-powered tools, such as machine learning algorithms for predicting and optimizing T cell-mediated anti-tumor responses. Variations may also involve using different nanomaterials or IoT-enabled bioreactors to enhance T cell expansion and viability.

Potential Commercial Applications and Market

The enhanced CAR-T cell therapy system has significant commercial potential in the cancer treatment market, particularly in personalized medicine and targeted therapies. The system's ability to improve monitoring, control, and personalized treatment can lead to better patient outcomes and increased adoption in clinical settings.

Original Patent Information

Patent NumberUS 11,857,574
TitleGenetically engineered T cells with Regnase-1 and/or TGFBRII disruption have improved functionality and persistence
Assignee(s)CRISPR THERAPEUTICS AG