Human PBMC models serve as a critical preclinical platform for recapitulating human immune responses, enabling the evaluation of immunotherapies and the study of immune-related adverse events such as CRS. Creative Biolabs' Human PBMC Model Development Service is tailored for CRS management. Leveraging advanced humanized mouse systems and robust engraftment techniques, we provide a physiologically relevant human immune context for accurate risk assessment and therapeutic screening. We offer clients a validated, customizable model to investigate CRS mechanisms, predict immunotoxicity, and support the development of safer and more effective immunomodulatory strategies.
The human PBMC model is a humanized mouse model featuring a reconstituted human immune system through the engraftment of human PBMC cells into immunodeficient mice. This platform serves as a valuable preclinical tool for recapitulating human immune responses, enabling the evaluation of immunotherapeutic strategies, drug toxicity testing, and mechanistic studies of immune-related diseases. More importantly, the human PBMC model provides a reliable preclinical basis for modeling CRS pathogenesis, assessing immunotherapy-related risks, and developing targeted intervention strategies.
Fig.1 Engraftment of human PBMC-derived HSCs in immunodeficient mice.1
Creative Biolabs' Human PBMC Model Development Service provides a physiologically relevant platform for predictive assessment of cytokine release syndrome risk. Utilizing primary human immune cells, we deliver quantitative, dose-responsive profiling of proinflammatory cytokine release to support your immunotherapeutic safety evaluation. Our human-relevant approach enables accurate risk stratification, informs clinical dosing strategies, and facilitates comparative candidate selection.
We deliver a comprehensive solution for CRS assessment, offering predictive, human-relevant models and deep mechanistic insights to guide your critical safety decisions.
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How does the PBMC model predict clinical CRS risk compared to whole blood assays?
While whole blood assays are suitable for fully soluble agents, our purified model allows for precise control over cell density and is ideal for complex therapeutics like plate-immobilized antibodies. We also offer co-culture options to better mimic the microenvironment. We recommend discussing your specific therapeutic with our team to select the most predictive format.
Is the high donor variability of PBMCs a concern for reliable results?
Donor variability is a genuine concern, which is why we maintains a rigorous donor qualification process. We use highly qualified, pre-screened donors and recommend testing your agent across multiple donors to provide robust statistical data that accounts for genetic diversity, giving you a more reliable risk assessment.
We offer tailored human PBMC model development and immunogenicity testing services, specifically designed to support the assessment of CRS. By choosing our service, you gain a trusted partner committed to providing physiologically relevant insights and robust data to help de-risk your therapeutic programs.
"The ability to quickly pair the in vivo PBMC efficacy data with the in vitro CRS risk prediction assay was invaluable. This integrated safety checkpoint, utilizing human PBMCs, facilitated our application strategy and provided crucial data for our safety filing."— A. K. Rob***on, Head of Translational Sciences, Cell Therapy Institute.
"Using Creative Biolabs' Human PBMC Model Development Service in our research has significantly improved the reproducibility of our anti-PD-1 efficacy studies. The technical consistency across donors and the robust flow cytometry data on TILs allowed us to confidently select our lead candidate."— Dr. M. Smi***h, Research Director, BioPharma R&D.
To explore how a scientific partnership can advance your immuno-oncology program toward the clinic, contact our specialists to initiate a customized project discussion.
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All products and services are For Research Use Only and CANNOT be used in the treatment or diagnosis of disease.
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