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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....

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2018
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.
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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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