Abstract 6694: Monocyte-derived dendritic cells for antigen-specific T cell activation

Abstract This study describes an efficient workflow to generate functional dendritic cells (DCs) from human peripheral blood monocytes and their application in antigen-specific T cell activation assays. Monocytes were differentiated into mature DCs expressing high levels of co-stimulatory molecules and MHC molecules. When pulsed with specific antigens and co-cultured with autologous T cells, these DCs effectively activated CD4+, CD8+, and regulatory T cell populations, as demonstrated by proliferation assays and cytokine profiling. The differential activation kinetics between T cell subsets provided insights into the temporal dynamics of antigen-specific immune responses. Our workflow demonstrates a standardized approach that offers a reliable research platform to investigate DC-T cell interactions, evaluate vaccine candidates, and assess antigen-specific T cell responses. Furthermore, our reproducible workflow may serve as a valuable tool for applications in immunology research, including vaccine development, cancer immunotherapy, and autoimmune condition studies. Citation Format: Kaitlin Hsu, Jessica Voce, Amy Zhao, Jessie Ni. Monocyte-derived dendritic cells for antigen-specific T cell activation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6694.

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Publication Details

Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6694
Primary Topic
Immunotherapy and Immune Responses
Type
article
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article

Abstract 6694: Monocyte-derived dendritic cells for antigen-specific T cell activation

Kaitlin Hsu, Amy H. Zhao, Jessie Ni, Jessica Voce
Cancer Research
Immunotherapy and Immune Responses
article

Abstract 6694: Monocyte-derived dendritic cells for antigen-specific T cell activation

Kaitlin Hsu, Amy H. Zhao, Jessie Ni, Jessica Voce
article en

Abstract

Abstract This study describes an efficient workflow to generate functional dendritic cells (DCs) from human peripheral blood monocytes and their application in antigen-specific T cell activation assays. Monocytes were differentiated into mature DCs expressing high levels of co-stimulatory molecules and MHC molecules. When pulsed with specific antigens and co-cultured with autologous T cells, these DCs effectively activated CD4+, CD8+, and regulatory T cell populations, as demonstrated by proliferation assays and cytokine profiling. The differential activation kinetics between T cell subsets provided insights into the temporal dynamics of antigen-specific immune responses. Our workflow demonstrates a standardized approach that offers a reliable research platform to investigate DC-T cell interactions, evaluate vaccine candidates, and assess antigen-specific T cell responses. Furthermore, our reproducible workflow may serve as a valuable tool for applications in immunology research, including vaccine development, cancer immunotherapy, and autoimmune condition studies. Citation Format: Kaitlin Hsu, Jessica Voce, Amy Zhao, Jessie Ni. Monocyte-derived dendritic cells for antigen-specific T cell activation [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6694.

Cancer ResearchVol. 86(7_Supplement)
BioLegend (United States) (US)
Good health and well-being
Openalex Percentile: Top 8%
Immunotherapy and Immune Responses
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