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RNA neoantigen vaccines prime long-lived CD8+ T cells in pancreatic cancer

素数(序理论) 病毒学 胰腺癌 CD8型 细胞毒性T细胞 核糖核酸 生物 医学 癌症研究 免疫学 癌症 抗原 遗传学 组合数学 数学 基因 体外
作者
Zachary Sethna,Pablo Guasp,Charlotte Reiche,Martina Milighetti,Nicholas Ceglia,Erin Patterson,Jayon Lihm,George C. Payne,Olga Lyudovyk,Luis A. Rojas,Nan Pang,Akihiro Ohmoto,Masataka Amisaki,Abderezak Zebboudj,Zagaa Odgerel,Emmanuel M. Bruno,Siqi Linsey Zhang,C. K. Cheng,Yuval Elhanati,Evelyna Derhovanessian
出处
期刊:Nature [Nature Portfolio]
卷期号:639 (8056): 1042-1051 被引量:167
标识
DOI:10.1038/s41586-024-08508-4
摘要

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.
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