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Adverse Effects Associated with Clinical Applications of CAR Engineered T Cells

Overview of attention for article published in Archivum Immunologiae et Therapiae Experimentalis, February 2018
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Title
Adverse Effects Associated with Clinical Applications of CAR Engineered T Cells
Published in
Archivum Immunologiae et Therapiae Experimentalis, February 2018
DOI 10.1007/s00005-018-0507-9
Pubmed ID
Authors

Zohreh Sadat Badieyan, Sayed Shahabuddin Hoseini

Abstract

Cancer has been ranked as the second leading cause of death in the United States. To reduce cancer mortality, immunotherapy is gaining momentum among other therapeutic modalities, due to its impressive results in clinical trials. The genetically engineered T cells expressing chimeric antigen receptors (CARs) are emerging as a new approach in cancer immunotherapy, with the most successful outcomes in the refractory/relapse hematologic malignancies. However, the widespread clinical applications are limited by adverse effects some of which are life-threatening. Strategies to reduce the chance of side effects as well as close monitoring, rapid diagnosis and proper treatment of side effects are necessary to take the most advantages of this valuable therapy. Here we review the reported toxicities associated with CAR engineered T cells, the strategies to ameliorate the toxicity, and further techniques and designs leading to a safer CAR T-cell therapy.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 30 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 30 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 8 27%
Student > Master 6 20%
Student > Doctoral Student 4 13%
Student > Ph. D. Student 3 10%
Other 2 7%
Other 2 7%
Unknown 5 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 5 17%
Agricultural and Biological Sciences 5 17%
Medicine and Dentistry 5 17%
Pharmacology, Toxicology and Pharmaceutical Science 3 10%
Immunology and Microbiology 2 7%
Other 3 10%
Unknown 7 23%