A New Frontier in Tumor Eradication: Harnessing <i>In Vivo</i> Cellular Reprogramming for Durable Cancer Immunotherapy

Tumors evade immune detection by downregulating antigen presentation and hindering immune responses. Type 1 conventional dendritic cells (cDC1s) are vital in stimulating cytotoxic T cells against tumors. Ascic et al. are now demonstrating the <i>in situ</i> ability of PU.1, IRF8, and BATF3 (PIB) transcription factors to directly reprogram a plethora of tumors bypassing the suppressive effects of the tumor microenvironment, and leading to overall tumor regression while eliciting a systemic immune response that can protect from secondary tumor induction.

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Publication Details

Journal
Cellular Reprogramming
Published
2024-10-01
DOI
https://doi.org/10.1089/cell.2024.0077
Primary Topic
CAR-T cell therapy research
Type
article
Field-Weighted Citation Impact
0.00

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article

A New Frontier in Tumor Eradication: Harnessing In Vivo Cellular Reprogramming for Durable Cancer Immunotherapy

Constantinos Chronis
Cellular Reprogramming
CAR-T cell therapy research
article

A New Frontier in Tumor Eradication: Harnessing In Vivo Cellular Reprogramming for Durable Cancer Immunotherapy

Constantinos Chronis
article en

Abstract

Tumors evade immune detection by downregulating antigen presentation and hindering immune responses. Type 1 conventional dendritic cells (cDC1s) are vital in stimulating cytotoxic T cells against tumors. Ascic et al. are now demonstrating the <i>in situ</i> ability of PU.1, IRF8, and BATF3 (PIB) transcription factors to directly reprogram a plethora of tumors bypassing the suppressive effects of the tumor microenvironment, and leading to overall tumor regression while eliciting a systemic immune response that can protect from secondary tumor induction.

Cellular ReprogrammingVol. 26(5)
University of Illinois Chicago (US)
National Institutes of Health, National Heart, Lung, and Blood Institute
Zero hunger
Openalex Percentile: Top 69%
CAR-T cell therapy research
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