| Literature DB >> 34715028 |
Lewis Au1, Emine Hatipoglu2, Marc Robert de Massy3, Kevin Litchfield4, Gordon Beattie3, Andrew Rowan4, Desiree Schnidrig5, Rachael Thompson6, Fiona Byrne5, Stuart Horswell7, Nicos Fotiadis8, Steve Hazell9, David Nicol10, Scott T C Shepherd1, Annika Fendler5, Robert Mason11, Lyra Del Rosario11, Kim Edmonds11, Karla Lingard11, Sarah Sarker11, Mary Mangwende11, Eleanor Carlyle11, Jan Attig6, Kroopa Joshi3, Imran Uddin12, Pablo D Becker13, Mariana Werner Sunderland13, Ayse Akarca14, Ignazio Puccio14, William W Yang14, Tom Lund15, Kim Dhillon14, Marcos Duran Vasquez3, Ehsan Ghorani3, Hang Xu4, Charlotte Spencer5, José I López16, Anna Green17, Ula Mahadeva17, Elaine Borg14, Miriam Mitchison14, David A Moore18, Ian Proctor14, Mary Falzon14, Lisa Pickering11, Andrew J S Furness11, James L Reading3, Roberto Salgado19, Teresa Marafioti14, Mariam Jamal-Hanjani20, George Kassiotis6, Benny Chain21, James Larkin11, Charles Swanton22, Sergio A Quezada23, Samra Turajlic24.
Abstract
ADAPTeR is a prospective, phase II study of nivolumab (anti-PD-1) in 15 treatment-naive patients (115 multiregion tumor samples) with metastatic clear cell renal cell carcinoma (ccRCC) aiming to understand the mechanism underpinning therapeutic response. Genomic analyses show no correlation between tumor molecular features and response, whereas ccRCC-specific human endogenous retrovirus expression indirectly correlates with clinical response. T cell receptor (TCR) analysis reveals a significantly higher number of expanded TCR clones pre-treatment in responders suggesting pre-existing immunity. Maintenance of highly similar clusters of TCRs post-treatment predict response, suggesting ongoing antigen engagement and survival of families of T cells likely recognizing the same antigens. In responders, nivolumab-bound CD8+ T cells are expanded and express GZMK/B. Our data suggest nivolumab drives both maintenance and replacement of previously expanded T cell clones, but only maintenance correlates with response. We hypothesize that maintenance and boosting of a pre-existing response is a key element of anti-PD-1 mode of action.Entities:
Keywords: T cell receptor; TCR clonal maintenance; TCR clonal replacement; anti-PD-1; autopsy; clear cell renal cell carcinoma; human endogenous retrovirus; multiregion; nivolumab
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Year: 2021 PMID: 34715028 PMCID: PMC8599450 DOI: 10.1016/j.ccell.2021.10.001
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743