CAR T cells: engineered immune cells to treat brain cancers and beyond.
Zoufang HuangSaikat DewanjeePratik ChakrabortyNiraj Kumar JhaAbhijit DeyMoumita GangopadhyayXuan-Yu ChenJian WangSaurabh Kumar JhaPublished in: Molecular cancer (2023)
Malignant brain tumors rank among the most challenging type of malignancies to manage. The current treatment protocol commonly entails surgery followed by radiotherapy and/or chemotherapy, however, the median patient survival rate is poor. Recent developments in immunotherapy for a variety of tumor types spark optimism that immunological strategies may help patients with brain cancer. Chimeric antigen receptor (CAR) T cells exploit the tumor-targeting specificity of antibodies or receptor ligands to direct the cytolytic capacity of T cells. Several molecules have been discovered as potential targets for immunotherapy-based targeting, including but not limited to EGFRvIII, IL13Rα2, and HER2. The outstanding clinical responses to CAR T cell-based treatments in patients with hematological malignancies have generated interest in using this approach to treat solid tumors. Research results to date support the astounding clinical response rates of CD19-targeted CAR T cells, early clinical experiences in brain tumors demonstrating safety and evidence for disease-modifying activity, and the promise for further advances to ultimately assist patients clinically. However, several variable factors seem to slow down the progress rate regarding treating brain cancers utilizing CAR T cells. The current study offers a thorough analysis of CAR T cells' promise in treating brain cancer, including design and delivery considerations, current strides in clinical and preclinical research, issues encountered, and potential solutions.
Keyphrases
- white matter
- resting state
- cancer therapy
- minimally invasive
- early stage
- induced apoptosis
- newly diagnosed
- stem cells
- squamous cell carcinoma
- mental health
- cell death
- end stage renal disease
- machine learning
- mesenchymal stem cells
- cell proliferation
- young adults
- radiation induced
- binding protein
- acute coronary syndrome
- rectal cancer
- patient reported
- surgical site infection