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A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers
Around 40% of humans and Tasmanian devils (Sarcophilus harrisii) develop cancer in their lifetime, compared to less than 10% for most species. In addition, devils are affected by two of the three known transmissible cancers in mammals. Immune checkpoint immunotherapy has transformed human medicine,...
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/PMC7458443/ https://www.ncbi.nlm.nih.gov/pubmed/32937435 http://dx.doi.org/10.1126/sciadv.aba5031 |
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author | Flies, Andrew S. Darby, Jocelyn M. Lennard, Patrick R. Murphy, Peter R. Ong, Chrissie E. B. Pinfold, Terry L. De Luca, Alana Lyons, A. Bruce Woods, Gregory M. Patchett, Amanda L. |
author_facet | Flies, Andrew S. Darby, Jocelyn M. Lennard, Patrick R. Murphy, Peter R. Ong, Chrissie E. B. Pinfold, Terry L. De Luca, Alana Lyons, A. Bruce Woods, Gregory M. Patchett, Amanda L. |
author_sort | Flies, Andrew S. |
collection | PubMed |
description | Around 40% of humans and Tasmanian devils (Sarcophilus harrisii) develop cancer in their lifetime, compared to less than 10% for most species. In addition, devils are affected by two of the three known transmissible cancers in mammals. Immune checkpoint immunotherapy has transformed human medicine, but a lack of species-specific reagents has limited checkpoint immunology in most species. We developed a cut-and-paste reagent development system and used the fluorescent fusion protein system to show that immune checkpoint interactions are conserved across 160,000,000 years of evolution, CD200 is highly expressed on transmissible tumor cells, and coexpression of CD200R1 can block CD200 surface expression. The system’s versatility across species was demonstrated by fusing a fluorescent reporter to a camelid-derived nanobody that binds human programmed death ligand 1. The evolutionarily conserved pathways suggest that naturally occurring cancers in devils and other species can be used to advance our understanding of cancer and immunological tolerance. |
format | Online Article Text |
id | pubmed-7458443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74584432020-09-16 A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers Flies, Andrew S. Darby, Jocelyn M. Lennard, Patrick R. Murphy, Peter R. Ong, Chrissie E. B. Pinfold, Terry L. De Luca, Alana Lyons, A. Bruce Woods, Gregory M. Patchett, Amanda L. Sci Adv Research Articles Around 40% of humans and Tasmanian devils (Sarcophilus harrisii) develop cancer in their lifetime, compared to less than 10% for most species. In addition, devils are affected by two of the three known transmissible cancers in mammals. Immune checkpoint immunotherapy has transformed human medicine, but a lack of species-specific reagents has limited checkpoint immunology in most species. We developed a cut-and-paste reagent development system and used the fluorescent fusion protein system to show that immune checkpoint interactions are conserved across 160,000,000 years of evolution, CD200 is highly expressed on transmissible tumor cells, and coexpression of CD200R1 can block CD200 surface expression. The system’s versatility across species was demonstrated by fusing a fluorescent reporter to a camelid-derived nanobody that binds human programmed death ligand 1. The evolutionarily conserved pathways suggest that naturally occurring cancers in devils and other species can be used to advance our understanding of cancer and immunological tolerance. American Association for the Advancement of Science 2020-07-01 /pmc/articles/PMC7458443/ /pubmed/32937435 http://dx.doi.org/10.1126/sciadv.aba5031 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 Flies, Andrew S. Darby, Jocelyn M. Lennard, Patrick R. Murphy, Peter R. Ong, Chrissie E. B. Pinfold, Terry L. De Luca, Alana Lyons, A. Bruce Woods, Gregory M. Patchett, Amanda L. A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
title | A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
title_full | A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
title_fullStr | A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
title_full_unstemmed | A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
title_short | A novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
title_sort | novel system to map protein interactions reveals evolutionarily conserved immune evasion pathways on transmissible cancers |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458443/ https://www.ncbi.nlm.nih.gov/pubmed/32937435 http://dx.doi.org/10.1126/sciadv.aba5031 |
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