Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/82502
Title: Clec9A + dendritic cells are not essential for antitumor CD8 + T cell responses induced by poly I:C immunotherapy
Authors: Gilfillan, Connie B.
Kuhn, Sabine
Baey, Camille
Hyde, Evelyn J.
Yang, Jianping
Ruedl, Christiane
Ronchese, Franca
Keywords: Science::Biological sciences
Dendritic Cells
CD8+ T Cell
Issue Date: 2018
Source: Gilfillan, C. B., Kuhn, S., Baey, C., Hyde, E. J., Yang, J., Ruedl, C., & Ronchese, F. (2018). Clec9A + dendritic cells are not essential for antitumor CD8 + T cell responses induced by poly I:C immunotherapy. Journal of Immunology, 200(8), 2978-2986. doi:10.4049/jimmunol.1701593
Series/Report no.: Journal of Immunology
Abstract: In the steady state, tumors harbor several populations of dendritic cells (DCs) and myeloid cells that are key regulators of the intratumoral immune environment. Among these cells, migratory CD103+ cross-presenting DCs are thought to be critical for tumor-specific CTL responses and tumor resistance. However, it is unclear whether this prominent role also extends to immunotherapy. We used a murine orthotopic mammary tumor model, as well as Clec9A–diphtheria toxin receptor mice that can be depleted of the specialized cross-presenting CD8α+ and CD103+ DC1 subsets, to investigate the role of these DCs in immunotherapy. Treatment with monosodium urate crystals and mycobacteria at the tumor site delayed tumor growth and required DC1s for efficacy. In contrast, treatment with poly I:C was equally effective regardless of DC1 depletion. Neither treatment affected myeloid-derived suppressor cell numbers in the spleen or tumor. Similar experiments using subcutaneous B16 melanoma tumors in BATF3-knockout mice confirmed that CD103+ DCs were not necessary for successful poly I:C immunotherapy. Nevertheless, adaptive immune responses were essential for the response to poly I:C, because mice depleted of CD8+ T cells or all DC subsets were unable to delay tumor growth. In vivo experiments showed that DC1 and DC2 subsets were able to take up tumor Ags, with DC2s making up the larger proportion of lymph node DCs carrying tumor material. Both DC subsets were able to cross-present OVA to OT-I T cells in vitro. Thus, immunotherapy with poly I:C enables multiple DC subsets to cross-present tumor Ag for effective antitumor immune responses.
URI: https://hdl.handle.net/10356/82502
http://hdl.handle.net/10220/49073
ISSN: 0022-1767
DOI: 10.4049/jimmunol.1701593
Rights: © 2018 The American Association of Immunologists, Inc. All rights reserved.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

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