Tumor-dependent myeloid and lymphoid cell recruitment in genO-BRGSF-HIS mice: a novel tool for evaluating immune therapies

Martin GH
genOway
September 17, 2025
Front Immunol
https://pubmed.ncbi.nlm.nih.gov/41041306/

This article is currently being updated. View its version on PubMed.

https://pubmed.ncbi.nlm.nih.gov/41041306/

Research summary

This study characterizes the immune composition and tumor response in genO-BRGSF-HIS humanized mice, reconstituted with human CD34⁺ stem cells. Functional human immune subsets including myeloid cells, dendritic cells, NK cells, γδ T cells, and T cells are recruited into tumors in a tumor-type and tumor-size dependent manner. The model is validated for testing immunotherapies including T-cell engagers in an in vivo humanized context.

Key outcome of the study

Tumor-infiltrating human myeloid and lymphoid cells show functional activation. Immune cell recruitment patterns vary based on tumor model and burden. The model supports in vivo testing of immunotherapies and exhibits long-term immune cell persistence without major toxicity.

Model

genO-BRGSF-HIS humanized mouse, reconstituted with human CD34⁺ HSCs — genOway-developed

TARGET:
Not applicable
Synonyms:
Not applicable

Keywords

Humanized mouse, immuno-oncology, tumor immune infiltration, functional myeloid and lymphoid cell evaluation, T-cell engager testing

Technical specifications

CD34⁺ HSC engraftment, exogenous Flt3L to support myeloid lineage, subcutaneous tumor xenografts using human cell lines, flow cytometry of immune compartments, cytokine and activation marker profiling, immunotherapy readouts in vivo

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genO‑BRGSF‑HIS

genO‑BRGSF‑HIS mice possess the most functional reconstituted human immune system currently on the market and are highly relevant for translational research.

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