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In vivo models grafted with human immune cells are essential for CAR-T therapy, GvHD, and tumor immunity research. When humanizing mice, peripheral blood mononuclear cells (PBMC) are of particular interest because they can quickly be implanted in immunodeficient mice. The human-derived cells in humanized PBMC mice are mainly T cells, which are suitable for various studies that require T cell immune response. Meanwhile, T cells can also over-immunize the recipient mice, which can cause graft-versus-host disease (GvHD), and cause the mice to die after a few weeks. Therefore, the humanized PBMC (hu-PBMC) mouse model is very suitable for short-term studies that require powerful effectors and memory T cells and NK cell functions.
The PBMC Hu-NSG mouse model from Creative Biolabs is a research-ready mouse model that can be provided upon request to be shipped to your institution or to participate in custom drug efficacy studies performed by our CAR-T preclinical in vivo evaluation scientists.
Humanized PBMC NSG mice models are used as in vivo models to study and evaluate tumor immunity, cell therapy, and GvHD. This model uses adult peripheral blood mononuclear cells with the fastest engraftment rate and supports short-term in vivo experiments that require mature T cell function. Created with adult peripheral blood mononuclear cells, it can be quickly engrafted and allows short-term studies that require mature human T cells. However, humanized PBMC mice show a low level of human B cells with no de novo immune response. The low B cell level is due to the decrease in the proportion of B cells over time, reflecting the strong expansion of T cells. In general, the humanized PBMC model can target T cell functions (such as immune checkpoint inhibitors/agonists, CAR-T cell therapy) to gain insight into human tumor immunology and therapeutic efficacy.
CD34+ HSC Hu-NSG Mice Model | PBMC Hu-NSG Mice Model | |
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Inject human peripheral blood mononuclear cells (hu-PBMC) into female NSG mice. The mice can be shipped to customers within a few days after implantation. Implantation (mainly T cells) will increase over time but is limited by the development of graft-versus-host disease.
Fig.1 Engraftment of PBMC into NSG mice.
Our NSG mouse models have a higher degree of immunodeficiency. It lacks NK cells while lacking T cells and B cells, and innate immunity is compromised. The NSG model is very suitable for human tumor cell transplantation (CDX), human tumor tissue transplantation (PDX) for immune reconstruction.
Highlights
Fig.2 Establishment of PBMC hu-NSG PDX model.
PBMC Hu-NSG is an ideal choice for long-term in vivo research in the field of immunology and cell therapy. Specifically, they can be used to evaluate the CAR-T therapies including but not limited to: monitor CAR-T distribution in vivo, determine CAR-T persistency, and monitor Cytokine Release Syndromes.
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