Humanized Mice Laboratory’s Post

In a collaboration with Tikva Allocell Pte Ltd, B7-H3 CAR EBVST cells were tested on Patient-Derived Xenograft (PDX) humanized mouse model. Significant tumour regression and modulation of the Tumour Microenvironment (TME) to promote tumour clearance was observed. Our Cytokine Release Syndrome (CRS) humanized mouse model demonstrated a markedly reduced risk of CRS associated with B7H3.CAR EBVST treatment. Key findings from our PDX & CRS humanized mouse model in this study: 1.    Tumour Regression: B7H3.CAR EBVSTs induced dramatic regression, with barely detectable tumours by the study's endpoint. 2.    T Cell Infiltration: There was significant infiltration of human T cells in PDX tumours from B7H3.CAR EBVST-treated mice. 3.    Improved Survival: B7H3.CAR EBVST treatment significantly improved survival compared to untreated EBVST treatment. 4.    Lower Cytokine Levels: Serum levels of human cytokines were significantly lower in B7H3.CAR EBVST-treated CRS humanized mice models compared to CD19.CAR ATC-treated mice. Using our humanized mouse model was crucial in revealing these insights, underscoring their importance in advancing cancer research and immunotherapy. Read the full article here: https://lnkd.in/ei2HkbMv #HumanizedMice #CancerResearch #Immunotherapy #CART #SolidTumor #CancerTherapy #ScientificBreakthroughs

B7-H3-Targeting Chimeric Antigen Receptors Epstein Barr Virus Specific T Cells Provides a Tumor Agnostic Off-The-Shelf Therapy Against B7-H3 Positive Solid Tumors

B7-H3-Targeting Chimeric Antigen Receptors Epstein Barr Virus Specific T Cells Provides a Tumor Agnostic Off-The-Shelf Therapy Against B7-H3 Positive Solid Tumors

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