In vitro-generated Tc17 cells present a memory phenotype and serve as a reservoir of Tc1 cells in vivo
dc.contributor.author | Flores-Santibáñez, F. | |
dc.contributor.author | Cuadra, B. | |
dc.contributor.author | Fernández, D. | |
dc.contributor.author | Rosemblatt, M.V. | |
dc.contributor.author | Núñez, S. | |
dc.contributor.author | Cruz, P. | |
dc.contributor.author | Gálvez-Cancino, F. | |
dc.contributor.author | César Cárdenas, J. | |
dc.contributor.author | Lladser, A. | |
dc.contributor.author | Rosemblatt, M. | |
dc.contributor.author | Bono, M.R. | |
dc.contributor.author | Sauma, D. | |
dc.date.accessioned | 2018-08-21T15:27:27Z | |
dc.date.available | 2018-08-21T15:27:27Z | |
dc.date.issued | 2018-02 | |
dc.description | Indexación: Scopus. | es_ES |
dc.description.abstract | Memory CD8+ T cells are ideal candidates for cancer immunotherapy because they can mediate long-term protection against tumors. However, the therapeutic potential of different in vitro-generated CD8+ T cell effector subsets to persist and become memory cells has not been fully characterized. Type 1 CD8+ T (Tc1) cells produce interferon-γ and are endowed with high cytotoxic capacity, whereas IL-17-producing CD8+ T (Tc17) cells are less cytotoxic but display enhanced self-renewal capacity. We sought to evaluate the functional properties of in vitro-generated Tc17 cells and elucidate their potential to become long lasting memory cells. Our results show that in vitro-generated Tc17 cells display a greater in vivo persistence and expansion in response to secondary antigen stimulation compared to Tc1 cells. When transferred into recipient mice, Tc17 cells persist in secondary lymphoid organs, present a recirculation behavior consistent with central memory T cells, and can shift to a Tc1 phenotype. Accordingly, Tc17 cells are endowed with a higher mitochondrial spare respiratory capacity than Tc1 cells and express higher levels of memory-related molecules than Tc1 cells. Together, these results demonstrate that in vitro-generated Tc17 cells acquire a central memory program and provide a lasting reservoir of Tc1 cells in vivo, thus supporting the use of Tc17 lymphocytes in the design of novel and more effective therapies. | es_ES |
dc.description.uri | https://www.frontiersin.org/articles/10.3389/fimmu.2018.00209/full | |
dc.identifier.citation | Frontiers in Immunology, 9(FEB), art. no. 209. | es_ES |
dc.identifier.issn | 1664-3224 | |
dc.identifier.other | DOI: 10.3389/fimmu.2018.00209 | |
dc.identifier.uri | http://repositorio.unab.cl/xmlui/handle/ria/6727 | |
dc.language.iso | en | es_ES |
dc.publisher | Frontiers Media | es_ES |
dc.subject | CD8+ T cell memory | es_ES |
dc.subject | Homing | es_ES |
dc.subject | Oxidative metabolism | es_ES |
dc.subject | Persistence | es_ES |
dc.subject | Secondary expansion | es_ES |
dc.subject | Tc17 cells | es_ES |
dc.title | In vitro-generated Tc17 cells present a memory phenotype and serve as a reservoir of Tc1 cells in vivo | es_ES |
dc.type | Artículo | es_ES |
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