mRNA Therapeutics & Cancer Vaccines

Personalized neoantigen mRNA vaccines, lipid-nanoparticle delivery, self-amplifying and circular RNA and mRNA therapeutics beyond infectious disease.

223 papersnewest Oct 2, 2026

Most influential

  • Personalized RNA neoantigen vaccines stimulate T cells in pancreatic cancer

    Abstract Pancreatic ductal adenocarcinoma (PDAC) is lethal in 88% of patients 1 , yet harbours mutation-derived T cell neoantigens that are suitable for vaccines 2,3 . Here in a phase I trial of adjuvant autogene cevumeran, an individualized neoantigen vaccine based on uridine mRNA–lipoplex nanoparticles, we synthesized mRNA neoantigen vaccines in real time …

    Abstract excerpt by Luis Alfonso Rojas et al., CC-BY, https://doi.org/10.1038/s41586-023-06063-y; truncated.

    Article1,431 citationsdoi:10.1038/s41586-023-06063-y
  • mRNA vaccine for cancer immunotherapy

    mRNA vaccines have become a promising platform for cancer immunotherapy. During vaccination, naked or vehicle loaded mRNA vaccines efficiently express tumor antigens in antigen-presenting cells (APCs), facilitate APC activation and innate/adaptive immune stimulation. mRNA cancer vaccine precedes other conventional vaccine platforms due to high potency, safe …

    Abstract excerpt by Lei Miao et al., CC-BY, https://doi.org/10.1186/s12943-021-01335-5; truncated.

    Review935 citationsdoi:10.1186/s12943-021-01335-5
  • RNA neoantigen vaccines prime long-lived CD8+ T cells in pancreatic cancer

    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 …

    Abstract excerpt by Zachary M. Sethna et al., CC-BY, https://doi.org/10.1038/s41586-024-08508-4; truncated.

    Article334 citationsdoi:10.1038/s41586-024-08508-4
  • Targeting cancer with mRNA–lipid nanoparticles: key considerations and future prospects
    Review376 citationsdoi:10.1038/s41571-023-00811-9
  • Neoantigen vaccine: an emerging tumor immunotherapy

    Genetic instability of tumor cells often leads to the occurrence of a large number of mutations, and expression of non-synonymous mutations can produce tumor-specific antigens called neoantigens. Neoantigens are highly immunogenic as they are not expressed in normal tissues. They can activate CD4+ and CD8+ T cells to generate immune response and have the pot…

    Abstract excerpt by Peng M et al., CC-BY, https://doi.org/10.1186/s12943-019-1055-6; truncated.

    Review558 citationsdoi:10.1186/s12943-019-1055-6
  • mRNA vaccine–induced neoantigen-specific T cell immunity in patients with gastrointestinal cancer
    Article426 citationsdoi:10.1172/jci134915
  • mRNA therapeutics in cancer immunotherapy

    Synthetic mRNA provides a template for the synthesis of any given protein, protein fragment or peptide and lends itself to a broad range of pharmaceutical applications, including different modalities of cancer immunotherapy. With the ease of rapid, large scale Good Manufacturing Practice-grade mRNA production, mRNA is ideally poised not only for off-the shel…

    Abstract excerpt by Jan David Beck et al., CC-BY, https://doi.org/10.1186/s12943-021-01348-0; truncated.

    Review385 citationsdoi:10.1186/s12943-021-01348-0
  • Relationships Between Immune Landscapes, Genetic Subtypes and Responses to Immunotherapy in Colorectal Cancer

    Colorectal cancer (CRC) is highly heterogeneous at the genetic and molecular level, which has major repercussions on the efficacy of immunotherapy. A small subset of CRCs exhibit microsatellite instability (MSI), a molecular indicator of defective DNA mismatch repair (MMR), but the majority are microsatellite-stable (MSS). The high tumor mutational burden (T…

    Abstract excerpt by Picard E et al., CC-BY, https://doi.org/10.3389/fimmu.2020.00369; truncated.

    Review432 citationsdoi:10.3389/fimmu.2020.00369
  • Personalized neoantigen vaccine and pembrolizumab in advanced hepatocellular carcinoma: a phase 1/2 trial

    Programmed cell death protein 1 (PD-1) inhibitors have modest efficacy as a monotherapy in hepatocellular carcinoma (HCC). A personalized therapeutic cancer vaccine (PTCV) may enhance responses to PD-1 inhibitors through the induction of tumor-specific immunity. We present results from a single-arm, open-label, phase 1/2 study of a DNA plasmid PTCV (GNOS-PV0…

    Abstract excerpt by Yarchoan M et al., CC-BY, https://doi.org/10.1038/s41591-024-02894-y; truncated.

    Article225 citationsdoi:10.1038/s41591-024-02894-y
  • Self-Amplifying RNA Vaccines Give Equivalent Protection against Influenza to mRNA Vaccines but at Much Lower Doses

    New vaccine platforms are needed to address the time gap between pathogen emergence and vaccine licensure. RNA-based vaccines are an attractive candidate for this role: they are safe, are produced cell free, and can be rapidly generated in response to pathogen emergence. Two RNA vaccine platforms are available: synthetic mRNA molecules encoding only the anti…

    Abstract excerpt by Vogel AB et al., CC-BY, https://doi.org/10.1016/j.ymthe.2017.11.017; truncated.

    Article420 citationsdoi:10.1016/j.ymthe.2017.11.017
  • Self-amplifying RNA SARS-CoV-2 lipid nanoparticle vaccine candidate induces high neutralizing antibody titers in mice

    The spread of the SARS-CoV-2 into a global pandemic within a few months of onset motivates the development of a rapidly scalable vaccine. Here, we present a self-amplifying RNA encoding the SARS-CoV-2 spike protein encapsulated within a lipid nanoparticle (LNP) as a vaccine. We observe remarkably high and dose-dependent SARS-CoV-2 specific antibody titers in…

    Abstract excerpt by McKay PF et al., CC-BY, https://doi.org/10.1038/s41467-020-17409-9; truncated.

    Article378 citationsdoi:10.1038/s41467-020-17409-9
  • Efficient Nanovaccine Delivery in Cancer Immunotherapy
    Review374 citationsdoi:10.1021/acsnano.7b00978
  • Individualized, heterologous chimpanzee adenovirus and self-amplifying mRNA neoantigen vaccine for advanced metastatic solid tumors: phase 1 trial interim results
    Article242 citationsdoi:10.1038/s41591-022-01937-6
  • A shared neoantigen vaccine combined with immune checkpoint blockade for advanced metastatic solid tumors: phase 1 trial interim results
    Article158 citationsdoi:10.1038/s41591-024-02851-9
  • Personalized Cancer Vaccines: Clinical Landscape, Challenges, and Opportunities
    Review287 citationsdoi:10.1016/j.ymthe.2020.09.038

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