Tumor-associated antigen (TAA) T-cell receptor (TCR) gene-engineered T cells exhibit great potential in antitumor immunotherapy. Considering the high costs and low availability of patient-derived peripheral blood T cells, substantial efforts have been made to explore alternatives to natural T cells. We previously reported that enforced expression of converted B cells into induced T (iT) cells Here, we successfully regenerated naive OT1 (major histocompatibility complex I restricted ovalbumin antigen) iT cells (OT1-iT) by expressing in pro-pre-B cells in the OT1 transgenic mouse. The OT1-iT cells can be activated and expanded in the presence of tumor cells. Particularly, these regenerated OT1-iT cells effectively eradicated tumor cells expressing the TAA (ovalbumin) both and This study provides insights into the translational applications of blood lineage-transdifferentiated T cells in immunotherapy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7368548PMC
http://dx.doi.org/10.1136/jitc-2019-000498DOI Listing

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