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Fc Effector Function Contributes to the Activity of Human Anti-CTLA-4 Antibodies

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posted on 2018-04-10, 13:33 authored by F. Arce Vargas, A. J. S. Furness, K. Litchfield, K. Joshi, R. Rosenthal, E. Ghorani, I. Solomon, M. H. Lesko, N. Ruef, C. Roddie, J. Y. Henry, L. Spain, A. Ben Aissa, A. Georgiou, Y. N. S. Wong, M. Smith, D. Strauss, A. Hayes, D. Nicol, T. O'Brien, L. Mårtensson, A. Ljungars, I. Teige, B. Frendéus, K. Harrington, A. Melcher, A. Wotherspoon, N. Francis, B. Challacombe, A. Fernando, S. Hazell, A. Chandra, L. Pickering, J. Lynch, S. Rudman, S. Chowdhury, K. Harrison-Phipps, M. Varia, C. Horsfield, A. Polson, G. Stamp, M. O'Donnell, W. Drake, P. Hill, D. Hrouda, E. Mayer, J. Olsburgh, G. Kooiman, K. O'Connor, G. Stewart, M. Aitchison, M. Tran, N. Fotiadis, H. Verma, J. Lopez, J. Lester, F. Morgan, M. Kornaszewska, R. Attanoos, H. Adams, H. Davies, Dean Fennell, J. Shaw, J. Le Quesne, A. Nakas, S. Rathinam, W. Monteiro, H. Marshall, L. Nelson, J. Bennett, J. Riley, L. Primrose, L. Martinson, G. Anand, S. Khan, M. Nicolson, K. Kerr, S. Palmer, H. Remmen, J. Miller, K. Buchan, M. Chetty, L. Gomersall
(Summary) 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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Citation

Cancer Cell, 2018, 33 (4), pp. 649–663.e4

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Cancer Research Centre

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  • VoR (Version of Record)

Published in

Cancer Cell

Publisher

Elsevier

issn

1535-6108

eissn

1878-3686

Acceptance date

2018-02-15

Copyright date

2018

Available date

2018-04-10

Publisher version

http://www.cell.com/cancer-cell/fulltext/S1535-6108(18)30063-1

Language

en

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