Journal Article DKFZ-2026-01834

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Efficient generation of human cDC1-like cells to detect and enhance tumor-reactive T cells via CD4+ T cell help.

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2026
Cell Press Cambridge, MA

Cell reports / Methods nn, nn () [10.1016/j.crmeth.2026.101533]
 GO

Abstract: Classical type 1 dendritic cells (cDC1s) are crucial to anti-tumor immunity by cross-presenting tumor antigens and priming cytotoxic CD8+ T lymphocytes (CTLs). Licensing via CD4+ T cell help endows cDC1s with enhanced cross-presentation and CTL-priming capacity, making them a promising tool to improve adoptive T cell therapies. However, the scarcity of primary human cDC1s limits their in-depth translational investigation and application. Here, we describe a method to efficiently generate DCs in vitro from CD34+c-KIT+ progenitors in non-mobilized peripheral blood. This DC population is enriched for cDC1-like cells that respond to CD4+ T cell help by upregulation of key molecules involved in antigen cross-presentation and T cell costimulation. Upon CD4+ T cell-mediated licensing, the progenitor-derived DC promotes tumor-specific CTL priming and facilitates detection of rare tumor antigen-specific CD8+ T cells in blood and tumor tissues. This DC culture platform incorporating CD4+ T cell help provides a scalable system for immunomonitoring and optimizing adoptive T cell therapies in cancer.

Keyword(s): CP: cancer biology ; CP: immunology ; adoptive cell therapy ; blood progenitor ; cDC1-licensing ; cDC1-like cell generation ; tumor antigen-specific CTL

Classification:

Note: epub

Contributing Institute(s):
  1. NWG Krebs-Immunregulation (D250)
Research Program(s):
  1. 314 - Immunologie und Krebs (POF4-314) (POF4-314)

Appears in the scientific report 2026
Database coverage:
Medline ; DOAJ ; Article Processing Charges ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; DOAJ Seal ; Emerging Sources Citation Index ; Fees ; IF < 5 ; JCR ; PubMed Central ; SCOPUS ; Web of Science Core Collection
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 Record created 2026-07-23, last modified 2026-07-24



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