Personalized GVHD Mitigation Systems

Publication ID: 24-11857610_0005_PTD
Published: October 28, 2025
Category:Future Evolutions & Paradigm Shifts

Legal Citation

pr1or.art Inc., “Personalized GVHD Mitigation Systems,” Published Technical Disclosure No. 24-11857610_0005_PTD, Published October 28, 2025, available at https://archive.pr1or.art/24-11857610_0005_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. 11,857,610.

Summary of the Inventive Concept

A next-generation system for mitigating graft versus host disease (GVHD) after hematopoietic cell transplantation (HCT) by leveraging AI-driven dosing regimens, genomic profiling, and real-time monitoring to provide personalized treatment and reduce the risk of GVHD.

Background and Problem Solved

The original patent disclosed methods for reducing the risk of GVHD after HCT by administering alpha-1 antitrypsin (A1AT) according to specific schedules. However, these methods have limitations, including the lack of personalized dosing and real-time monitoring. The new inventive concept addresses these limitations by introducing AI-driven dosing regimens, genomic profiling, and real-time monitoring to provide more effective and targeted treatment.

Detailed Description of the Inventive Concept

The new inventive concept comprises a system for mitigating GVHD, which includes a personalized, AI-driven dosing regimen of A1AT tailored to an individual patient's genomic profile. The dosing regimen is adjusted in real-time based on machine learning algorithms analyzing the patient's response to treatment. Additionally, the system includes a deep learning model for predicting the likelihood of GVHD onset, a nanosensor-based device for in vivo monitoring of A1AT levels, a method for generating personalized, 3D-printed implants, and a system for remote monitoring and management of GVHD.

Novelty and Inventive Step

The new claims introduce the use of AI-driven dosing regimens, genomic profiling, and real-time monitoring, which are not present in the original patent. The combination of these elements provides a novel and non-obvious approach to mitigating GVHD.

Alternative Embodiments and Variations

Alternative embodiments of the inventive concept could include the use of different AI algorithms, genomic profiling techniques, or monitoring devices. Additionally, the system could be adapted for use in other types of transplantation or for treating other diseases.

Potential Commercial Applications and Market

The inventive concept has significant commercial potential in the field of hematopoietic cell transplantation, particularly in the treatment of GVHD. The system could be marketed to hospitals, research institutions, and pharmaceutical companies, with potential applications in personalized medicine, regenerative medicine, and remote patient monitoring.

CPC Classifications

SectionClassGroup
A A61 A61K38/57
A A61 A61K35/12
A A61 A61P37/06
A A61 A61K2035/124

Field of Art

Medical biotechnology focused on hematopoietic cell transplantation (HCT), immunotherapy, and personalized medicine, with expertise in immunosuppressive treatments, protein therapeutics, and advanced monitoring technologies

Person of Ordinary Skill (PHOSITA) Profile

A medical researcher or clinician with advanced degrees in biomedical engineering, immunology, or medical technology, possessing expertise in transplantation medicine, AI-driven medical technologies, and personalized treatment strategies

Obviousness Rationale

A PHOSITA would recognize that the PTD's AI-driven personalization of A1AT dosing represents a predictable extension of existing personalized medicine approaches, leveraging known machine learning techniques to optimize an established therapeutic method for GVHD mitigation. The combination of genomic profiling, real-time monitoring, and adaptive dosing represents an incremental technological improvement that would be obvious to a skilled practitioner seeking to enhance treatment precision.

Obvious Combinations & Variations

Source Patent Element
Fixed A1AT dosing schedule for GVHD prevention
PTD Variation
AI-driven personalized dosing regimen adjusted in real-time based on patient response
Obviousness Reasoning
Personalized medicine is a known technique in medical treatment, and applying machine learning to optimize dosing would be an obvious approach for improving therapeutic outcomes
Source Patent Element
Standard GVHD risk assessment methods
PTD Variation
Deep learning model for predicting GVHD onset using genomic and clinical variables
Obviousness Reasoning
Predictive modeling using machine learning is a standard technique in medical diagnostics, and applying it to GVHD risk assessment represents a logical extension of existing risk stratification methods
Source Patent Element
Traditional A1AT administration methods
PTD Variation
Nanosensor-based in vivo monitoring of A1AT levels with real-time feedback
Obviousness Reasoning
Continuous monitoring technologies are well-established in medical treatment, and integrating such systems with protein therapeutic administration is a predictable technological improvement
Source Patent Element
Standard HCT treatment protocols
PTD Variation
3D-printed personalized A1AT-eluting implants for tissue regeneration
Obviousness Reasoning
Customized medical devices and localized drug delivery are known techniques, and combining 3D printing with targeted therapeutic approaches represents an obvious innovation in personalized medicine
35 U.S.C. § 103 Summary: Based on the teachings of US Patent 11857610 and the disclosed technological variations, a person of ordinary skill in the art would find the claimed personalized GVHD mitigation system obvious, as the combination of AI-driven dosing, genomic profiling, and real-time monitoring represents a predictable and incremental advancement in existing medical treatment methodologies for preventing and managing acute graft versus host disease.

Original Patent Information

Patent NumberUS 11,857,610
TitleMethods for reducing risk of onset of acute graft versus host disease after hematopoietic cell transplantation
Assignee(s)CSL Behring AG