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Updated: Feb 12, 2026

Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
Published on: February 16, 2015
Engineering T cells for adoptive therapy: outsmarting the tumor
1Laboratory of Tumor Immunology, Department of Medical Oncology, Erasmus MC-Cancer Institute, Rotterdam, The Netherlands.
Abstract:
Adoptive transfer of T cells gene-engineered with antigen-specific receptors, whether it be chimeric antigen receptors (CARs) or T cell receptors (TCRs), has proven its feasibility and therapeutic potential in the treatment of tumors. Despite clinical successes, the majority of patients experiences no or non-sustainable clearance of solid tumors, which is attributed to local T cell evasive mechanisms. A rapidly expanding understanding of molecular and cellular events that contribute to a reduction in numbers and/or activation of intra-tumor T cells has facilitated the development of gene-engineering strategies, enabling T cells to counter immune tolerance. Here, we present an overview of gene-engineering approaches and considerations to improve tumor-selectivity and effectiveness of adoptively transferred T cells.
Insights
Gene-engineered T cells show promise for cancer treatment but struggle with solid tumors due to immune evasion. New strategies aim to enhance T cell effectiveness and tumor targeting for better patient outcomes.
Area of Science:
- Immunology
- Oncology
- Gene Therapy
Background:
- Adoptive T cell therapy using engineered receptors (CARs, TCRs) is feasible for tumors.
- Solid tumors often resist treatment due to local T cell evasion and immune tolerance.
- Understanding intra-tumor T cell suppression is key to improving therapies.
Purpose of the Study:
- To review gene-engineering strategies for adoptive T cell therapy.
- To enhance T cell tumor-selectivity and therapeutic effectiveness.
- To overcome immune evasion in solid tumors.
Main Methods:
- Overview of current gene-engineering approaches for T cells.
- Analysis of mechanisms of T cell evasion in the tumor microenvironment.
- Discussion of strategies to improve T cell function and persistence.
Main Results:
- Engineered T cells demonstrate therapeutic potential but face challenges in solid tumors.
- Local immune evasion mechanisms limit the efficacy of adoptive T cell transfer.
- Gene-engineering offers solutions to enhance T cell anti-tumor activity.
Conclusions:
- Adoptive T cell therapy requires advanced gene-engineering to overcome solid tumor resistance.
- Strategies to improve T cell tumor-selectivity and counter immune tolerance are crucial.
- Further development of gene-editing techniques will enhance cancer immunotherapy effectiveness.
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