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Updated: May 27, 2025

Flow Cytometry-Based Isolation and Therapeutic Evaluation of Tumor-Infiltrating Lymphocytes in a Mouse Model of Pancreatic Cancer
Published on: January 17, 2025
RNA neoantigen vaccines prime long-lived CD8+ T cells in pancreatic cancer
Zachary Sethna1,2,3,4, Pablo Guasp1,2, Charlotte Reiche1,2
1Immuno-Oncology Service, Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
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.
Insights
mRNA-lipoplex neoantigen vaccines show promise for pancreatic cancer by generating long-lived T cells. This approach may significantly improve recurrence-free survival in patients with pancreatic ductal adenocarcinoma (PDAC).
Area of Science:
- Immunology
- Oncology
- Vaccinology
Background:
- Generating long-lived, functional T cells specific for tumor antigens is a critical challenge for cancer vaccines, particularly in low-mutation cancers like pancreatic ductal adenocarcinoma (PDAC).
- Existing treatments for PDAC have limited efficacy, highlighting the need for novel therapeutic strategies.
Purpose of the Study:
- To evaluate the efficacy of an individualized neoantigen mRNA-lipoplex vaccine (autogene cevumeran) in combination with atezolizumab and modified FOLFIRINOX in patients with PDAC.
- To assess the longevity, magnitude, and functional state of vaccine-induced T cells and their correlation with clinical outcomes.
Main Methods:
- A phase 1 clinical trial involving surgery, atezolizumab, autogene cevumeran, and modified FOLFIRINOX in PDAC patients.
- Extended follow-up (median 3.2 years) to assess recurrence-free survival (RFS).
- Utilized PhenoTrack, a novel computational strategy, to trace T cell phenotypes and lifespan, assessing T cell avidity and effector function.
Main Results:
- Responders with vaccine-induced T cells (n=8) demonstrated significantly prolonged RFS (median not reached) compared to non-responders (n=8; median RFS 13.4 months).
- Autogene cevumeran induced CD8+ T cell clones with an average estimated lifespan of 7.7 years, with a significant portion exhibiting multi-decade potential.
- Approximately 86% of T cell clones per patient persisted at substantial frequencies three years post-vaccination, maintaining high avidity and effector functions.
Conclusions:
- Autogene cevumeran induces de novo CD8+ T cells with multiyear longevity, substantial magnitude, and durable effector functions, potentially delaying PDAC recurrence.
- Adjuvant mRNA-lipoplex neoantigen vaccines represent a promising strategy to overcome a pivotal obstacle in cancer vaccination for PDAC.
- The findings suggest that vaccine-induced T cell response is a critical determinant of long-term clinical benefit in PDAC.
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