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An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA
V-domain immunoglobulin (Ig) suppressor of T cell activation (VISTA) is an immune checkpoint that maintains peripheral T cell quiescence and inhibits anti-tumor immune responses. VISTA functions by dampening the interaction between myeloid cells and T cells, orthogonal to PD-1 and other checkpoints...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494997/ https://www.ncbi.nlm.nih.gov/pubmed/32938950 http://dx.doi.org/10.1038/s41598-020-71519-4 |
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author | Mehta, Nishant Maddineni, Sainiteesh Kelly, Ryan L. Lee, Robert B. Hunter, Sean A. Silberstein, John L. Parra Sperberg, R. Andres Miller, Caitlyn L. Rabe, Amanda Labanieh, Louai Cochran, Jennifer R. |
author_facet | Mehta, Nishant Maddineni, Sainiteesh Kelly, Ryan L. Lee, Robert B. Hunter, Sean A. Silberstein, John L. Parra Sperberg, R. Andres Miller, Caitlyn L. Rabe, Amanda Labanieh, Louai Cochran, Jennifer R. |
author_sort | Mehta, Nishant |
collection | PubMed |
description | V-domain immunoglobulin (Ig) suppressor of T cell activation (VISTA) is an immune checkpoint that maintains peripheral T cell quiescence and inhibits anti-tumor immune responses. VISTA functions by dampening the interaction between myeloid cells and T cells, orthogonal to PD-1 and other checkpoints of the tumor-T cell signaling axis. Here, we report the use of yeast surface display to engineer an anti-VISTA antibody that binds with high affinity to mouse, human, and cynomolgus monkey VISTA. Our anti-VISTA antibody (SG7) inhibits VISTA function and blocks purported interactions with both PSGL-1 and VSIG3 proteins. SG7 binds a unique epitope on the surface of VISTA, which partially overlaps with other clinically relevant antibodies. As a monotherapy, and to a greater extent as a combination with anti-PD1, SG7 slows tumor growth in multiple syngeneic mouse models. SG7 is a promising clinical candidate that can be tested in fully immunocompetent mouse models and its binding epitope can be used for future campaigns to develop species cross-reactive inhibitors of VISTA. |
format | Online Article Text |
id | pubmed-7494997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74949972020-09-18 An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA Mehta, Nishant Maddineni, Sainiteesh Kelly, Ryan L. Lee, Robert B. Hunter, Sean A. Silberstein, John L. Parra Sperberg, R. Andres Miller, Caitlyn L. Rabe, Amanda Labanieh, Louai Cochran, Jennifer R. Sci Rep Article V-domain immunoglobulin (Ig) suppressor of T cell activation (VISTA) is an immune checkpoint that maintains peripheral T cell quiescence and inhibits anti-tumor immune responses. VISTA functions by dampening the interaction between myeloid cells and T cells, orthogonal to PD-1 and other checkpoints of the tumor-T cell signaling axis. Here, we report the use of yeast surface display to engineer an anti-VISTA antibody that binds with high affinity to mouse, human, and cynomolgus monkey VISTA. Our anti-VISTA antibody (SG7) inhibits VISTA function and blocks purported interactions with both PSGL-1 and VSIG3 proteins. SG7 binds a unique epitope on the surface of VISTA, which partially overlaps with other clinically relevant antibodies. As a monotherapy, and to a greater extent as a combination with anti-PD1, SG7 slows tumor growth in multiple syngeneic mouse models. SG7 is a promising clinical candidate that can be tested in fully immunocompetent mouse models and its binding epitope can be used for future campaigns to develop species cross-reactive inhibitors of VISTA. Nature Publishing Group UK 2020-09-16 /pmc/articles/PMC7494997/ /pubmed/32938950 http://dx.doi.org/10.1038/s41598-020-71519-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mehta, Nishant Maddineni, Sainiteesh Kelly, Ryan L. Lee, Robert B. Hunter, Sean A. Silberstein, John L. Parra Sperberg, R. Andres Miller, Caitlyn L. Rabe, Amanda Labanieh, Louai Cochran, Jennifer R. An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA |
title | An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA |
title_full | An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA |
title_fullStr | An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA |
title_full_unstemmed | An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA |
title_short | An engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human VISTA |
title_sort | engineered antibody binds a distinct epitope and is a potent inhibitor of murine and human vista |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7494997/ https://www.ncbi.nlm.nih.gov/pubmed/32938950 http://dx.doi.org/10.1038/s41598-020-71519-4 |
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