Related Experiment Video
Updated: Nov 9, 2025

Testing Cancer Immunotherapeutics in a Humanized Mouse Model Bearing Human Tumors
Published on: December 16, 2022
Testing Cancer Immunotherapy in a Human Immune System Mouse Model: Correlating Treatment Responses to Human
Juan A Marín-Jiménez1, Anna Capasso2, Matthew S Lewis3
1Department of Medical Oncology, Catalan Institute of Oncology (ICO-L'Hospitalet), Barcelona, Spain.
Abstract:
Over the past decade, immunotherapies have revolutionized the treatment of cancer. Although the success of immunotherapy is remarkable, it is still limited to a subset of patients. More than 1500 clinical trials are currently ongoing with a goal of improving the efficacy of immunotherapy through co-administration of other agents. Preclinical, small-animal models are strongly desired to increase the pace of scientific discovery, while reducing the cost of combination drug testing in humans. Human immune system (HIS) mice are highly immune-deficient mouse recipients rtpeconstituted with human hematopoietic stem cells. These HIS-mice are capable of growing human tumor cell lines and patient-derived tumor xenografts. This model allows rapid testing of multiple, immune-related therapeutics for tumors originating from unique clinical samples. Using a cord blood-derived HIS-BALB/c-Rag2nullIl2rγnullSIRPαNOD (BRGS) mouse model, we summarize our experiments testing immune checkpoint blockade combinations in these mice bearing a variety of human tumors, including breast, colorectal, pancreatic, lung, adrenocortical, melanoma and hematological malignancies. We present in-depth characterization of the kinetics and subsets of the HIS in lymph and non-lymph organs and relate these to protocol development and immune-related treatment responses. Furthermore, we compare the phenotype of the HIS in lymph tissues and tumors. We show that the immunotype and amount of tumor infiltrating leukocytes are widely-variable and that this phenotype is tumor-dependent in the HIS-BRGS model. We further present flow cytometric analyses of immune cell subsets, activation state, cytokine production and inhibitory receptor expression in peripheral lymph organs and tumors. We show that responding tumors bear human infiltrating T cells with a more inflammatory signature compared to non-responding tumors, similar to reports of "responding" patients in human immunotherapy clinical trials. Collectively these data support the use of HIS mice as a preclinical model to test combination immunotherapies for human cancers, if careful attention is taken to both protocol details and data analysis.
Insights
Human immune system (HIS) mice enable testing of combination immunotherapies for various cancers. This preclinical model shows that responding tumors have inflammatory T cells, mirroring human clinical trial outcomes.
Area of Science:
- Oncology
- Immunology
- Preclinical Cancer Models
Background:
- Immunotherapies have transformed cancer treatment but benefit only a subset of patients.
- Over 1500 clinical trials investigate immunotherapy combinations to improve efficacy.
- Preclinical models are crucial for cost-effective combination drug testing.
Purpose of the Study:
- To evaluate human immune system (HIS) mice as a preclinical model for testing cancer immunotherapy combinations.
- To characterize the human immune system reconstitution and its response to immunotherapy in HIS mice bearing human tumors.
- To compare immune cell phenotypes in lymph tissues and tumors to treatment responses.
Main Methods:
- Utilized a cord blood-derived HIS-BALB/c-Rag2nullIl2rgnullSIRPαNOD (BRGS) mouse model.
- Engrafted BRGS mice with human tumor cell lines and patient-derived xenografts.
- Administered immune checkpoint blockade combinations and analyzed immune cell kinetics, subsets, activation, cytokine production, and receptor expression via flow cytometry.
Main Results:
- HIS-BRGS mice supported human tumor growth and allowed testing of immunotherapy combinations.
- The human immune system reconstitution and tumor-infiltrating leukocyte phenotype were variable and tumor-dependent.
- Responding tumors exhibited human T cells with a more inflammatory signature compared to non-responding tumors.
Conclusions:
- HIS mice serve as a valuable preclinical model for evaluating combination immunotherapies in diverse human cancers.
- Careful attention to protocol details and data analysis is essential for reliable results.
- The model recapitulates key aspects of human immunotherapy responses observed in clinical trials.
More Related Videos
06:08Assessment of Chimeric Antigen Receptor T Cell-Associated Toxicities Using an Acute Lymphoblastic Leukemia Patient-Derived Xenograft Mouse Model
Published on: February 10, 2023
05:15Production of Humanized Mouse via Thymic Renal Capsule Grafting, CD34+ Cells Injection, and Cytokine Delivery
Published on: September 27, 2021
Related Concept Videos
Mouse Models of Cancer Study
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...
Tumor Immunotherapy