[Limassol – 14.12.2022] InSysBio, one of the world’s pioneers of Quantitative Systems Pharmacology (QSP) modeling, launches the Oncology version of Immune Response Template (IRT). IRT in Oncology represents a QSP platform of immune system in cancer, simultaneously being a tool for development of QSP and mechanistic models related to tumor-specific immune response.
IRT is a part of InSysBio’s QSP software infrastructure being under constant development. The new IRT Onco version contains tumor and tumor-draining lymph node compartments that provide the opportunity to perform more accurate cancer modeling.
Initially, IRT is based on two main components. On the one hand, it is a database including a wide variety of features covering the immune system. On the other hand, it comprises Navigator that provides intuitive interface to interact with IRT Database. Thus, a modeler can apply calibrated sub-models exported from IRT as building blocks for particular purposes.
Veronika Musatova, Head of IRT development team, comments on the update, “Previously, IRT has been representing the immune system in general and now we have developed the version which is more eligible for immune response modeling in oncology projects. The initial Onco version describes core processes, and then we are going to include regulators of the processes and focus on parameters identification via the data obtained particularly from oncology research”.
IRT Onco version schemes include type of cells that involved in tumor immune response: different types of T cells, B cells, Dendritic cells, Natural killers, Macrophages, etc. Also, the platform covers the process of specific destruction of malignance cells by NK and CD8a cells. The core model of IRT Onco version currently embraces 311 cell processes describing reactions for 95 time dependent cell variables with 386 parameters. Moreover, complexes formation between 33 surface molecules species is described. Nearly 40% of equations parameters in the current version are identified by direct calculation or fitting.
List of IRT Onco main processes:
To learn the full content of Immune Response Template Onco, please visit irt.insysbio.com.
To get more information on any tool or leave your feedback, please feel free to contact us: support@insysbio.com
About InSysBio
InSysBio is a group of Quantitative Systems Pharmacology (QSP) companies located in Limassol, Cyprus (INSYSBIO CY Ltd), Edinburgh, UK (INSYSBIO UK LIMITED) and Moscow, Russia (INSYSBIO LLC). InSysBio was founded in 2004 and has an extensive track record of helping pharmaceutical companies to make right decisions on the critical stages of drug research and development by application of QSP modeling. InSysBio’s innovative QSP approach has already become a part of the drug development process implemented by our strategic partners: there are more than 100 completed projects in collaboration with leaders of pharmaceutical industry. For more information about InSysBio, its solutions and services, visit www.insysbio.com
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04 Sep 2024 16:07
Now B cells model reflects the current views on the processes
InSysBio launches Immune Response Template (IRT) version 3.6.3. IRT represents a QSP platform of immune system, simultaneously, being a tool for development of models related to immune system
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10 Sep 2024 18:36
InSysBio team to publish the new article in PSPJournal
The new article "Quantitative systems pharmacology model of α-synuclein pathology in Parkinson's disease-like mouse for investigation of passive immunotherapy mechanisms" by Olga Ivanova and Tatiana Karelina was published in PSPJournal at the end of August 2024
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11 Sep 2024 15:25
InSysBio to take part in ACoP 2024
InSysBio announces its participation in the 15th American Conference on Pharmacometrics (ACoP). Oleg Demin Jr, Scientific Director, Oncology & Immuno-Oncology, will be a co-chair and speaker of the session "Advancing QSP: From Virtual Patient To Digital Twin". InSysBio team is going to present its modeling services & software to optimize drug development at the Booth #11 and 9 posters in frames of the Conference
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