Author
Listed:
- Zachary Sethna
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Pablo Guasp
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Charlotte Reiche
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Martina Milighetti
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Nicholas Ceglia
(Memorial Sloan Kettering Cancer Center)
- Erin Patterson
(Memorial Sloan Kettering Cancer Center)
- Jayon Lihm
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- George Payne
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Olga Lyudovyk
(Memorial Sloan Kettering Cancer Center)
- Luis A. Rojas
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Nan Pang
(Memorial Sloan Kettering Cancer Center)
- Akihiro Ohmoto
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Masataka Amisaki
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Abderezak Zebboudj
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Zagaa Odgerel
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Emmanuel M. Bruno
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Siqi Linsey Zhang
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Charlotte Cheng
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Yuval Elhanati
(Memorial Sloan Kettering Cancer Center)
- Evelyna Derhovanessian
(BioNTech)
- Luisa Manning
(BioNTech)
- Felicitas Müller
(BioNTech)
- Ina Rhee
(Genentech)
- Mahesh Yadav
(Genentech)
- Taha Merghoub
(Weill Cornell Medical College)
- Jedd D. Wolchok
(Weill Cornell Medical College)
- Olca Basturk
(Memorial Sloan Kettering Cancer Center)
- Mithat Gönen
(Memorial Sloan Kettering Cancer Center)
- Andrew S. Epstein
(Memorial Sloan Kettering Cancer Center)
- Parisa Momtaz
(Memorial Sloan Kettering Cancer Center)
- Wungki Park
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Ryan Sugarman
(Memorial Sloan Kettering Cancer Center)
- Anna M. Varghese
(Memorial Sloan Kettering Cancer Center)
- Elizabeth Won
(Memorial Sloan Kettering Cancer Center)
- Avni Desai
(Memorial Sloan Kettering Cancer Center)
- Alice C. Wei
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Michael I. D’Angelica
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- T. Peter Kingham
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Kevin C. Soares
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- William R. Jarnagin
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Jeffrey Drebin
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Eileen M. O’Reilly
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
- Ira Mellman
(Genentech)
- Ugur Sahin
(BioNTech
Helmholtz Institute for Translational Oncology)
- Özlem Türeci
(BioNTech
Helmholtz Institute for Translational Oncology)
- Benjamin D. Greenbaum
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center
Weill Cornell Medical College)
- Vinod P. Balachandran
(Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center
Memorial Sloan Kettering Cancer Center)
Abstract
A fundamental challenge for cancer vaccines is to generate long-lived functional T cells that are specific for tumour antigens. Here we find that mRNA–lipoplex vaccines against somatic mutation-derived neoantigens may solve this challenge in pancreatic ductal adenocarcinoma (PDAC), a lethal cancer with few mutations. At an extended 3.2-year median follow-up from a phase 1 trial of surgery, atezolizumab (PD-L1 inhibitory antibody), autogene cevumeran1 (individualized neoantigen vaccine with backbone-optimized uridine mRNA–lipoplex nanoparticles) and modified (m) FOLFIRINOX (chemotherapy) in patients with PDAC, we find that responders with vaccine-induced T cells (n = 8) have prolonged recurrence-free survival (RFS; median not reached) compared with non-responders without vaccine-induced T cells (n = 8; median RFS 13.4 months; P = 0.007). In responders, autogene cevumeran induces CD8+ T cell clones with an average estimated lifespan of 7.7 years (range 1.5 to roughly 100 years), with approximately 20% of clones having latent multi-decade lifespans that may outlive hosts. Eighty-six percent of clones per patient persist at substantial frequencies approximately 3 years post-vaccination, including clones with high avidity to PDAC neoepitopes. Using PhenoTrack, a novel computational strategy to trace single T cell phenotypes, we uncover that vaccine-induced clones are undetectable in pre-vaccination tissues, and assume a cytotoxic, tissue-resident memory-like T cell state up to three years post-vaccination with preserved neoantigen-specific effector function. Two responders recurred and evidenced fewer vaccine-induced T cells. Furthermore, recurrent PDACs were pruned of vaccine-targeted cancer clones. Thus, in PDAC, autogene cevumeran induces de novo CD8+ T cells with multiyear longevity, substantial magnitude and durable effector functions that may delay PDAC recurrence. Adjuvant mRNA–lipoplex neoantigen vaccines may thus solve a pivotal obstacle for cancer vaccination.
Suggested Citation
Zachary Sethna & Pablo Guasp & Charlotte Reiche & Martina Milighetti & Nicholas Ceglia & Erin Patterson & Jayon Lihm & George Payne & Olga Lyudovyk & Luis A. Rojas & Nan Pang & Akihiro Ohmoto & Masata, 2025.
"RNA neoantigen vaccines prime long-lived CD8+ T cells in pancreatic cancer,"
Nature, Nature, vol. 639(8056), pages 1042-1051, March.
Handle:
RePEc:nat:nature:v:639:y:2025:i:8056:d:10.1038_s41586-024-08508-4
DOI: 10.1038/s41586-024-08508-4
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