Promoting the accumulation of tumor-specific T cells in tumor tissues by dendritic cell vaccines and chemokine-modulating agents

This protocol describes how to generate and use dendritic cells and combinatorial adjuvants to modulate tumor microenvironment and increase T-cell accumulation in tumors in vivo . This protocol describes how to induce large numbers of tumor-specific cytotoxic T cells (CTLs) in the spleens and lymph...

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Veröffentlicht in:Nature protocols 2018-02, Vol.13 (2), p.335-357
Hauptverfasser: Obermajer, Nataša, Urban, Julie, Wieckowski, Eva, Muthuswamy, Ravikumar, Ravindranathan, Roshni, Bartlett, David L, Kalinski, Pawel
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Sprache:eng
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Zusammenfassung:This protocol describes how to generate and use dendritic cells and combinatorial adjuvants to modulate tumor microenvironment and increase T-cell accumulation in tumors in vivo . This protocol describes how to induce large numbers of tumor-specific cytotoxic T cells (CTLs) in the spleens and lymph nodes of mice receiving dendritic cell (DC) vaccines and how to modulate tumor microenvironments (TMEs) to ensure effective homing of the vaccination-induced CTLs to tumor tissues. We also describe how to evaluate the numbers of tumor-specific CTLs within tumors. The protocol contains detailed information describing how to generate a specialized DC vaccine with augmented ability to induce tumor-specific CTLs. We also describe methods to modulate the production of chemokines in the TME and show how to quantify tumor-specific CTLs in the lymphoid organs and tumor tissues of mice receiving different treatments. The combined experimental procedure, including tumor implantation, DC vaccine generation, chemokine-modulating (CKM) approaches, and the analyses of tumor-specific systemic and intratumoral immunity is performed over 30–40 d. The presented ELISpot-based ex vivo CTL assay takes 6 h to set up and 5 h to develop. In contrast to other methods of evaluating tumor-specific immunity in tumor tissues, our approach allows detection of intratumoral T-cell responses to nonmanipulated weakly immunogenic cancers. This detection method can be performed using basic laboratory skills, and facilitates the development and preclinical evaluation of new immunotherapies.
ISSN:1754-2189
1750-2799
DOI:10.1038/nprot.2017.130