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Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies
With the use of a mouse model expressing human Fc-gamma receptors (FcγRs), we demonstrated that antibodies with isotypes equivalent to ipilimumab and tremelimumab mediate intra-tumoral regulatory T (Treg) cell depletion in vivo, increasing the CD8(+) to Treg cell ratio and promoting tumor rejection....
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904288/ https://www.ncbi.nlm.nih.gov/pubmed/29576375 http://dx.doi.org/10.1016/j.ccell.2018.02.010 |
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author | Arce Vargas, Frederick Furness, Andrew J.S. Litchfield, Kevin Joshi, Kroopa Rosenthal, Rachel Ghorani, Ehsan Solomon, Isabelle Lesko, Marta H. Ruef, Nora Roddie, Claire Henry, Jake Y. Spain, Lavinia Ben Aissa, Assma Georgiou, Andrew Wong, Yien Ning Sophia Smith, Myles Strauss, Dirk Hayes, Andrew Nicol, David O'Brien, Tim Mårtensson, Linda Ljungars, Anne Teige, Ingrid Frendéus, Björn Pule, Martin Marafioti, Teresa Gore, Martin Larkin, James Turajlic, Samra Swanton, Charles Peggs, Karl S. Quezada, Sergio A. |
author_facet | Arce Vargas, Frederick Furness, Andrew J.S. Litchfield, Kevin Joshi, Kroopa Rosenthal, Rachel Ghorani, Ehsan Solomon, Isabelle Lesko, Marta H. Ruef, Nora Roddie, Claire Henry, Jake Y. Spain, Lavinia Ben Aissa, Assma Georgiou, Andrew Wong, Yien Ning Sophia Smith, Myles Strauss, Dirk Hayes, Andrew Nicol, David O'Brien, Tim Mårtensson, Linda Ljungars, Anne Teige, Ingrid Frendéus, Björn Pule, Martin Marafioti, Teresa Gore, Martin Larkin, James Turajlic, Samra Swanton, Charles Peggs, Karl S. Quezada, Sergio A. |
author_sort | Arce Vargas, Frederick |
collection | PubMed |
description | With the use of a mouse model expressing human Fc-gamma receptors (FcγRs), we demonstrated that antibodies with isotypes equivalent to ipilimumab and tremelimumab mediate intra-tumoral regulatory T (Treg) cell depletion in vivo, increasing the CD8(+) to Treg cell ratio and promoting tumor rejection. Antibodies with improved FcγR binding profiles drove superior anti-tumor responses and survival. In patients with advanced melanoma, response to ipilimumab was associated with the CD16a-V158F high affinity polymorphism. Such activity only appeared relevant in the context of inflamed tumors, explaining the modest response rates observed in the clinical setting. Our data suggest that the activity of anti-CTLA-4 in inflamed tumors may be improved through enhancement of FcγR binding, whereas poorly infiltrated tumors will likely require combination approaches. |
format | Online Article Text |
id | pubmed-5904288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-59042882018-04-19 Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies Arce Vargas, Frederick Furness, Andrew J.S. Litchfield, Kevin Joshi, Kroopa Rosenthal, Rachel Ghorani, Ehsan Solomon, Isabelle Lesko, Marta H. Ruef, Nora Roddie, Claire Henry, Jake Y. Spain, Lavinia Ben Aissa, Assma Georgiou, Andrew Wong, Yien Ning Sophia Smith, Myles Strauss, Dirk Hayes, Andrew Nicol, David O'Brien, Tim Mårtensson, Linda Ljungars, Anne Teige, Ingrid Frendéus, Björn Pule, Martin Marafioti, Teresa Gore, Martin Larkin, James Turajlic, Samra Swanton, Charles Peggs, Karl S. Quezada, Sergio A. Cancer Cell Article With the use of a mouse model expressing human Fc-gamma receptors (FcγRs), we demonstrated that antibodies with isotypes equivalent to ipilimumab and tremelimumab mediate intra-tumoral regulatory T (Treg) cell depletion in vivo, increasing the CD8(+) to Treg cell ratio and promoting tumor rejection. Antibodies with improved FcγR binding profiles drove superior anti-tumor responses and survival. In patients with advanced melanoma, response to ipilimumab was associated with the CD16a-V158F high affinity polymorphism. Such activity only appeared relevant in the context of inflamed tumors, explaining the modest response rates observed in the clinical setting. Our data suggest that the activity of anti-CTLA-4 in inflamed tumors may be improved through enhancement of FcγR binding, whereas poorly infiltrated tumors will likely require combination approaches. Cell Press 2018-04-09 /pmc/articles/PMC5904288/ /pubmed/29576375 http://dx.doi.org/10.1016/j.ccell.2018.02.010 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Arce Vargas, Frederick Furness, Andrew J.S. Litchfield, Kevin Joshi, Kroopa Rosenthal, Rachel Ghorani, Ehsan Solomon, Isabelle Lesko, Marta H. Ruef, Nora Roddie, Claire Henry, Jake Y. Spain, Lavinia Ben Aissa, Assma Georgiou, Andrew Wong, Yien Ning Sophia Smith, Myles Strauss, Dirk Hayes, Andrew Nicol, David O'Brien, Tim Mårtensson, Linda Ljungars, Anne Teige, Ingrid Frendéus, Björn Pule, Martin Marafioti, Teresa Gore, Martin Larkin, James Turajlic, Samra Swanton, Charles Peggs, Karl S. Quezada, Sergio A. Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies |
title | Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies |
title_full | Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies |
title_fullStr | Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies |
title_full_unstemmed | Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies |
title_short | Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies |
title_sort | fc effector function contributes to the activity of human anti-ctla-4 antibodies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5904288/ https://www.ncbi.nlm.nih.gov/pubmed/29576375 http://dx.doi.org/10.1016/j.ccell.2018.02.010 |
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