The paradigm shift in treatment from Covid-19 to oncology with mRNA vaccines
Open accessAbstract
mRNA vaccines have gained popularity over the last decade as a versatile tool for developing novel therapeutics. The recent success of coronavirus disease (COVID-19) mRNA vaccine has unlocked the potential of mRNA technology as a powerful therapeutic platform. In this review, we apprise the literature on the various types of cancer vaccines, the novel platforms available for delivery of the vaccines, the recent progress in the RNA-based therapies and the evolving role of mRNA vaccines for various cancer indications, along with a future strategy to treat the patients. Literature reveals that despite multifaceted challenges in the development of mRNA vaccines, the promising and durable efficacy of the RNA in pre-clinical and clinical studies deserves consideration. The introduction of mRNA-transfected DC vaccine is an approach that has gained interest for cancer vaccine development due to its ability to circumvent the necessity of DC isolation, ex vivo cultivation and re-infusion. The selection of appropriate antigen of interest remains one of the major challenges for cancer vaccine development. The rapid development and large-scale production of mRNA platform has enabled for the development of both personalized vaccines (mRNA 4157, mRNA 4650 and RO7198457) and tetravalent vaccines (BNT111 and mRNA-5671). In addition, mRNA vaccines combined with checkpoint modulators and other novel medications that reverse immunosuppression show promise, however further research is needed to discover which combinations are most successful and the best dosing schedule for each component. Each delivery route (intradermal, subcutaneous, intra tumoral, intranodal, intranasal, intravenous) has its own set of challenges to overcome, and these challenges will decide the best delivery method. In other words, while developing a vaccine design, the underlying motivation should be a reasonable combination of delivery route and format. Exploring various administration routes and delivery route systems has boosted the development of mRNA vaccines.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
mRNA-5671/V941 is a tetravalent mutant KRAS mRNA vaccine containing sequences G12C, G12D, G12V, and G13D.
“Prior to the pandemic, Moderna used technology similar to the SARS-CoV-2 vaccine to develop mRNA-5671/V941, a tetravalent mutant KRAS mRNA vaccine containing sequences G12C, G12D, G12V, and G13D [83].”
From KRAS: Biology, Inhibition, and Mechanisms of Inhibitor Resistance (2024) · cites this paper as [83]
mRNA-5671 is a nanoparticle-formulated mRNA vaccine taken up by antigen-presenting cells and presented on the cell surface after translation, leading to T cell responses to mutant RAS neo-epitopes.
“mRNA-5671 (251), also known as V941, is a nanoparticle-formulated mRNA vaccine taken up by antigen-presenting cells and presented on the cell surface after translation, leading to T cell responses to the mutant RAS neo-epitopes.587”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [587]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 122 · Cited by 57
Research works printed but not linked: 2
- [22]Eric Lutz Yeo Charles J. Lillemoe Keith D. Biedrzycki Barbara Kobrin Barry Herman Joseph A lethally irradiated allogeneic granulocyte-macrophage colony stimulating factor-secreting tumor vaccine for pancreatic adenocarcinoma. A Phase II trial of safety, efficacy, and immune activation Ann Surg 253 2 2011 328 335 21217520 PMC3085934
- [90]Heistein JB, Acharya U. Malignant Melanoma. StatPearls Publishing; 2021. 29262210
- Authors
- Wei, J., & Hui, A.-M.
- Affiliations
- Fosun Pharma (China) (CN)
- Corresponding author
- Hui, Ai-Min
- ORCID
- Hui, Ai-Min
- Venue
- Cancer Treatment Reviews
- Publisher
- Elsevier BV
- Published
- 2022-06
- Volume
- 107
- Pages
- 102405
- ISSN
- 0305-7372 (ISSN-L)
- PMC
- PMC9068246
- OpenAlex
- W4229041892
- Cited by
- 57
- References
- 122
- Citations by year
- 2026: 8 · 2025: 10 · 2024: 14 · 2023: 21 · 2022: 4
- FWCI
- 1.29
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Cancer Treatment Reviews (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- mRNA vaccines, cancer vaccines, COVID-19 vaccines, dendritic cell vaccine, personalized cancer vaccines, tetravalent vaccine, immune checkpoint inhibitors, vaccine delivery routes, antigen selection, combination immunotherapy
- MeSH terms
- COVID-19, SARS-CoV-2, mRNA Vaccines, Humans, Neoplasms, RNA, Messenger, Vaccines, Synthetic, Cancer Vaccines
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review