Immunotherapy of human cancers using gene modified T lymphocytes
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Updated: Jun 19, 2026

Using the BLT Humanized Mouse as a Stem Cell based Gene Therapy Tumor Model
Published on: December 18, 2012
Juan F Vera1, Malcolm K Brenner, Gianpietro Dotti
1Center for Cell and Gene Therapy, Department of Medicine, Baylor College of Medicine, The Methodist Hospital and Texas Children's Hospital, 6621 Fannin Avenue, Houston, TX 77030, USA.
Abstract:
Adoptive T cell therapies can produce objective clinical responses in patients with hematologic and solid malignancies. Genetic manipulation of T lymphocytes has been proposed as a means of increasing the potency and range of this anti-tumor activity. We now review how coupling expression of transgenic receptors with countermeasures against potent tumor immune evasion strategies is proving highly effective in pre-clinical models and describe how these approaches are being evaluated in human subjects.
Insights
Adoptive T cell therapy shows promise for cancer treatment. Genetically engineered T cells, combined with strategies to overcome tumor immune evasion, are proving effective in preclinical models and are now being tested in human clinical trials.
Area of Science:
- Immunology
- Oncology
- Genetic Engineering
Background:
- Adoptive T cell therapy offers clinical responses in various cancers.
- Genetic modification of T cells can enhance anti-tumor activity.
- Tumors possess immune evasion strategies that limit therapy effectiveness.
Purpose of the Study:
- To review advancements in genetically engineered T cell therapies.
- To highlight the integration of transgenic receptors and immune evasion countermeasures.
- To discuss the clinical evaluation of these enhanced T cell therapies.
Main Methods:
- Review of pre-clinical data on engineered T cell therapies.
- Analysis of strategies combining transgenic receptors with immune evasion countermeasures.
- Examination of ongoing human clinical trials for these approaches.
Main Results:
- Coupling transgenic receptors with immune evasion countermeasures is highly effective in pre-clinical models.
- Engineered T cell therapies demonstrate increased potency and range against tumors.
- These advanced therapies are progressing to evaluation in human subjects.
Conclusions:
- Genetically engineered T cell therapies, incorporating immune evasion resistance, represent a promising frontier in cancer treatment.
- The combination of enhanced T cell function and tumor immune evasion neutralization is crucial for therapeutic success.
- Clinical evaluation in human subjects is underway, signifying the translation of these findings.
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