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Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context
Revealing the mechanisms that underlie the expansion of antitumor CD8(+) T cells that are associated with improved clinical outcomes is critical to improving immunotherapeutic management of melanoma. How the lymphatic system, which orchestrates the complex sensing of antigen by lymphocytes to mount...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732197/ https://www.ncbi.nlm.nih.gov/pubmed/33310857 http://dx.doi.org/10.1126/sciadv.abd7134 |
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author | O’Melia, M. J. Rohner, N. A. Manspeaker, M. P. Francis, D. M. Kissick, H. T. Thomas, S. N. |
author_facet | O’Melia, M. J. Rohner, N. A. Manspeaker, M. P. Francis, D. M. Kissick, H. T. Thomas, S. N. |
author_sort | O’Melia, M. J. |
collection | PubMed |
description | Revealing the mechanisms that underlie the expansion of antitumor CD8(+) T cells that are associated with improved clinical outcomes is critical to improving immunotherapeutic management of melanoma. How the lymphatic system, which orchestrates the complex sensing of antigen by lymphocytes to mount an adaptive immune response, facilitates this response in the context of malignancy is incompletely understood. To delineate the effects of lymphatic transport and tumor-induced lymphatic and lymph node (LN) remodeling on the elicitation of CD8(+) T cell immunity within LNs, we designed a suite of nanoscale biomaterial tools enabling the quantification of antigen access and presentation within the LN and resulting influence on T cell functions. The expansion of antigen-specific stem-like and cytotoxic CD8(+) T cell pools was revealed to be sensitive to the mechanism of lymphatic transport to LNs, demonstrating the potential for nanoengineering strategies targeting LNs to optimize cancer immunotherapy in eliciting antitumor CD8(+) T cell immunity. |
format | Online Article Text |
id | pubmed-7732197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-77321972020-12-18 Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context O’Melia, M. J. Rohner, N. A. Manspeaker, M. P. Francis, D. M. Kissick, H. T. Thomas, S. N. Sci Adv Research Articles Revealing the mechanisms that underlie the expansion of antitumor CD8(+) T cells that are associated with improved clinical outcomes is critical to improving immunotherapeutic management of melanoma. How the lymphatic system, which orchestrates the complex sensing of antigen by lymphocytes to mount an adaptive immune response, facilitates this response in the context of malignancy is incompletely understood. To delineate the effects of lymphatic transport and tumor-induced lymphatic and lymph node (LN) remodeling on the elicitation of CD8(+) T cell immunity within LNs, we designed a suite of nanoscale biomaterial tools enabling the quantification of antigen access and presentation within the LN and resulting influence on T cell functions. The expansion of antigen-specific stem-like and cytotoxic CD8(+) T cell pools was revealed to be sensitive to the mechanism of lymphatic transport to LNs, demonstrating the potential for nanoengineering strategies targeting LNs to optimize cancer immunotherapy in eliciting antitumor CD8(+) T cell immunity. American Association for the Advancement of Science 2020-12-11 /pmc/articles/PMC7732197/ /pubmed/33310857 http://dx.doi.org/10.1126/sciadv.abd7134 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles O’Melia, M. J. Rohner, N. A. Manspeaker, M. P. Francis, D. M. Kissick, H. T. Thomas, S. N. Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
title | Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
title_full | Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
title_fullStr | Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
title_full_unstemmed | Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
title_short | Quality of CD8(+) T cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
title_sort | quality of cd8(+) t cell immunity evoked in lymph nodes is compartmentalized by route of antigen transport and functional in tumor context |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7732197/ https://www.ncbi.nlm.nih.gov/pubmed/33310857 http://dx.doi.org/10.1126/sciadv.abd7134 |
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