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Generation of CAR T Cells for Adoptive Therapy in the Context of Glioblastoma Standard of Care
Published on: February 16, 2015
Adoptive cell therapy in paediatric extracranial solid tumours: current approaches and future challenges
Elisa Zappa1, Alice Vitali2, Kathleen Anders3
1Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands.
Adoptive cell therapy (ACT) shows promise for treating paediatric solid tumours. New strategies are being developed to overcome challenges like tumour immune evasion and T cell exhaustion for improved patient outcomes.
Area of Science:
- Oncology
- Immunology
- Cell Therapy
Background:
- Immunotherapy offers new hope for paediatric solid tumours resistant to conventional treatments.
- Adoptive cell therapy (ACT), especially with chimeric antigen receptor (CAR) T cells, is a leading immunotherapy approach.
- Paediatric solid tumours present challenges due to their immunosuppressive microenvironment and tumour-intrinsic factors affecting ACT efficacy.
Purpose of the Study:
- To review current ACT strategies for paediatric extracranial solid tumours.
- To evaluate preclinical and clinical evidence for promising ACT approaches.
- To identify challenges and future opportunities in ACT for paediatric oncology.
Main Methods:
- Review of scientific literature on ACT for paediatric solid tumours.
- Analysis of clinical trial data and preclinical studies.
- Discussion of novel cell engineering and combination therapy strategies.
Main Results:
- CAR T-cell therapy is a focal point in clinical studies for paediatric solid tumours.
- Tumour immune evasion and T cell dysfunction remain significant hurdles for ACT.
- Emerging strategies include innate-like lymphocytes, advanced cell engineering, and combination therapies.
Conclusions:
- ACT holds significant potential for treating paediatric solid tumours.
- Overcoming tumour immunosuppression and T cell exhaustion is critical for ACT success.
- Continued innovation in cell engineering and combination therapies is essential to improve outcomes for children with solid tumours.
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