Sethna Zachary, Guasp Pablo, Reiche Charlotte, Milighetti Martina, Ceglia Nicholas, Patterson Erin, Lihm Jayon, Payne George, Lyudovyk Olga, Rojas Luis A, Pang Nan, Ohmoto Akihiro, Amisaki Masataka, Zebboudj Abderezak, Odgerel Zagaa, Bruno Emmanuel M, Zhang Siqi Linsey, Cheng Charlotte, Elhanati Yuval, Derhovanessian Evelyna, Manning Luisa, Müller Felicitas, Rhee Ina, Yadav Mahesh, Merghoub Taha, Wolchok Jedd D, Basturk Olca, Gönen Mithat, Epstein Andrew S, Momtaz Parisa, Park Wungki, Sugarman Ryan, Varghese Anna M, Won Elizabeth, Desai Avni, Wei Alice C, D'Angelica Michael I, Kingham T Peter, Soares Kevin C, Jarnagin William R, Drebin Jeffrey, O'Reilly Eileen M, Mellman Ira, Sahin Ugur, Türeci Özlem, Greenbaum Benjamin D, Balachandran Vinod P
Immuno-Oncology Service, Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Hepatopancreatobiliary Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Nature. 2025 Mar;639(8056):1042-1051. doi: 10.1038/s41586-024-08508-4. Epub 2025 Feb 19.
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 cevumeran (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.
癌症疫苗面临的一个根本挑战是产生针对肿瘤抗原的长寿功能性T细胞。我们发现,针对体细胞突变衍生的新抗原的mRNA-脂质复合物疫苗可能解决胰腺导管腺癌(PDAC)这一具有少量突变的致命癌症中的这一挑战。在一项针对PDAC患者的手术、阿替利珠单抗(PD-L1抑制性抗体)、自体基因西沃美仑(一种采用骨架优化的尿苷mRNA-脂质复合物纳米颗粒的个体化新抗原疫苗)和改良(m)FOLFIRINOX(化疗)的1期试验的3.2年中位延长随访中,我们发现有疫苗诱导T细胞的应答者(n = 8)与没有疫苗诱导T细胞的无应答者(n = 8;中位无复发生存期[RFS]为13.4个月;P = 0.007)相比,无复发生存期延长(RFS;未达到中位值)。在应答者中,自体基因西沃美仑诱导出平均估计寿命为7.7年(范围为1.5至约100年)的CD8 T细胞克隆,约20%的克隆具有潜在的数十年寿命,可能比宿主活得更久。每位患者86%的克隆在接种疫苗后约3年仍以相当高的频率持续存在,包括对PDAC新表位具有高亲和力的克隆。使用PhenoTrack(一种追踪单个T细胞表型的新型计算策略),我们发现疫苗诱导的克隆在接种前的组织中无法检测到,并在接种疫苗后长达三年的时间里呈现出细胞毒性、组织驻留记忆样T细胞状态,同时保留新抗原特异性效应功能。两名应答者复发,且疫苗诱导的T细胞较少。此外,复发性PDAC中靶向疫苗的癌症克隆减少。因此,在PDAC中,自体基因西沃美仑诱导出具有多年寿命、大量且持久效应功能的新生CD8 T细胞,这可能会延迟PDAC的复发。因此,辅助性mRNA-脂质复合物新抗原疫苗可能解决癌症疫苗接种的一个关键障碍。