Application of Genome-Editing Technologies for Off-the-Shelf T Cell-Based Cancer Immunotherapy

AuthorZohreh Hakakzadehen
AuthorVahid Yekehfallahen
AuthorHamidreza Ebrahimiyanen
AuthorAli Sayadmaneshen
AuthorMohsen Basirien
OrcidHamidreza Ebrahimiyan [0000-0003-0689-1281]en
OrcidAli Sayadmanesh [0000-0003-2338-9840]en
OrcidMohsen Basiri [0000-0003-2512-7641]en
Issued Date2021-12-31en
AbstractGenetically, engineered T-cell therapy is a personalized treatment that has demonstrated considerable therapeutic potential for solid tumors and hematopoietic cancers. However, endogenous T-cell receptors (TCRs) on the surface of engineered T cells hamper their application in the allogeneic settings by inducing graft-versus-host disease, where endogenous TCRs on the surface of engineered T cells respond to the recipient’s tissues. Since the cause of this allogeneic response is the TCR complex on the surface of the engineered T cells, preventing the expression of TCR components on the surface of these cells is a promising strategy to address this challenge. This review discusses the production of allogeneic chimeric antigen receptor T cells using genome-editing methods.en
DOIhttps://doi.org/10.5812/pmco.116796en
KeywordGenome Editingen
KeywordChimeric Antigen Receptoren
KeywordCRISPRen
KeywordTALENen
KeywordZFNen
KeywordT-Cell Receptoren
KeywordCancer Immunotherapyen
PublisherBrieflandsen
TitleApplication of Genome-Editing Technologies for Off-the-Shelf T Cell-Based Cancer Immunotherapyen
TypeReview Articleen

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