CAR-T Cell Therapy Development for Triple Negative Breast Cancer

CAR-T Cell Therapy Development for Triple Negative Breast Cancer

Triple-negative breast cancer (TNBC) presents a significant therapeutic challenge due to its aggressive nature and lack of common hormone receptors. At Alfa Cytology, we provide specialized preclinical CRO services to support the development of CAR-T cell therapies tailored for TNBC. Our integrated platform encompasses target validation, CAR construct design, in vitro testing, and in vivo efficacy evaluation-accelerating the translation of innovative immunotherapies toward clinical readiness.

Our Services

Target Identification and Validation

Screening and validation of TNBC-specific antigens suitable for CAR-T therapy, using transcriptomic, proteomic, and tumor tissue profiling tools.

CAR Construct Design & Optimization

Design and in vitro optimization of custom CAR constructs, including scFv engineering, costimulatory domain selection, and transduction efficiency testing.

In Vitro Functional Evaluation

Comprehensive assays to assess CAR-T cytotoxicity, cytokine release, proliferation, and persistence against TNBC cell lines.

In Vivo Efficacy Studies

Evaluation of CAR-T cell antitumor activity using xenograft and syngeneic TNBC mouse models, including biodistribution and tumor regression analysis.

Key Advantages

TNBC-Focused Antigen Strategies Selection of novel or underexplored tumor-associated antigens ensures enhanced specificity for the heterogeneity of triple-negative breast tumors.
Modular and Flexible CAR Design CAR constructs are customized with modular domains to meet your preclinical goals—whether optimizing persistence, minimizing exhaustion, or improving safety profiles.
Physiologically Relevant Models Our validated 2D, 3D, and in vivo models reflect the complex tumor microenvironment of TNBC, providing reliable platforms for therapeutic screening.
IND-Enabling Preclinical Packages Comprehensive, publication-ready data packages are generated to support IND submissions and guide early-stage development decisions.

Download our brochure to explore how our preclinical CAR-T services can advance your TNBC research. For customized project planning and technical consultation, please contact us directly.

Case Study - In Vitro CAR-T Evaluation

HER2 CAR-T cells were co-cultured with MDA-MB-231 cells at varying effector-to-target ratios. HER2-specific CAR-T cells specifically recognized HER2+ tumor cells, shown by significantly increased IFNγ secretion, while unmodified (NT) T cells did not induce mIFNg release (Fig.1). HER2-specific CAR-T cells selectively killed MDA-MB-231 cells, whereas non-transduced T cells showed no cytotoxicity (Fig.2). These results demonstrate HER2-specific CAR activates mouse T cells and triggers tumor killing via antigen-dependent mechanisms.

HER2 CAR or NT T cells were co-cultured with HER2+ MDA-MB-231 cellsFig.1 HER2 CAR or NT T cells were co-cultured with HER2+ MDA-MB-231 cells at various T cell to tumor cell ratios.

Cytotoxicity assayFig.2 XTT-based cytotoxicity assay.

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