# From Design to Clinical Use: mRNA Vaccines for Infectious Diseases and Cancer

**Authors:** Yulin Cui, Ziyue Liang, Hua Cong

PMC · DOI: 10.3390/vaccines14030202 · Vaccines · 2026-02-25

## TL;DR

This paper reviews the progress and potential of mRNA vaccines in treating infectious diseases and cancer, highlighting their advantages and future directions.

## Contribution

The paper provides a comprehensive review of mRNA vaccine design, mechanisms, delivery systems, and clinical applications, identifying future research directions.

## Key findings

- mRNA vaccines can rapidly trigger both innate and adaptive immunity by mimicking natural viral infection.
- Delivery systems like lipid nanoparticles and exosomes are critical but face challenges like inefficiency and cost.
- mRNA vaccines show promising results in preclinical and clinical trials for diseases like SARS-CoV-2 and HIV.

## Abstract

mRNA vaccines represent a revolutionary advance in vaccinology, boasting advantages like rapid development, robust immunogenicity and flexible antigen design over traditional vaccines. This review systematically summarizes the core research progress of mRNA vaccines, including their structural composition with five functional elements and novel subtypes (linear mRNA, self-amplifying RNA, circular RNA) with unique biological characteristics and application value. It elaborates on the immune activation mechanism of mRNA vaccines, which mimic natural viral infection to trigger both innate and adaptive immunity, and analyzes mainstream delivery systems (lipid nanoparticles, dendritic cells, protamine, exosomes, polymers) with their respective performance, advantages and bottlenecks. This review also details the clinical application status of mRNA vaccines in infectious diseases (influenza, rabies, monkeypox, SARS-CoV-2, HIV, parasites) and cancer therapy, highlighting promising preclinical and clinical results of candidate vaccines and combined therapeutic regimens. Additionally, it addresses the current limitations of mRNA vaccines, such as delivery inefficiency, production costs, and cold chain constraints. Finally, this review prospects the future development direction, emphasizing that the optimization of delivery systems, antigen design and production processes will further promote the clinical translation and diversified application of mRNA vaccines in disease prevention and treatment.

## Linked entities

- **Diseases:** influenza (MONDO:0005812), rabies (MONDO:0019173), monkeypox (MONDO:0002594), SARS-CoV-2 (MONDO:0100096)

## Full-text entities

- **Genes:** CD209 (CD209 molecule) [NCBI Gene 30835] {aka CDSIGN, CLEC4L, DC-SIGN, DC-SIGN1, hDC-SIGN}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, TLR8 (toll like receptor 8) [NCBI Gene 51311] {aka CD288, IMD98, TLR-8, hTLR8}, mir-7 (mir-7 stem loop) [NCBI Gene 12798133] {aka 7, CR33042, CR42883, Dmel\CR42883, Dmel_CR33042, dme-miR-7}, IFIH1 (interferon induced with helicase C domain 1) [NCBI Gene 64135] {aka AGS7, Hlcd, IDDM19, IMD95, MDA-5, MDA5}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, TLR7 (toll like receptor 7) [NCBI Gene 51284] {aka IMD74, SLEB17, TLR7-like}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, DUSP5 (dual specificity phosphatase 5) [NCBI Gene 1847] {aka DUSP, HVH3}, PLAAT4 (phospholipase A and acyltransferase 4) [NCBI Gene 5920] {aka HRASLS4, HRSL4, PLA1/2-3, PLAAT-4, RARRES3, RIG1}, IFNA1 (interferon alpha 1) [NCBI Gene 3439] {aka IFL, IFN, IFN-ALPHA, IFN-alphaD, IFNA13, IFNA@}, MICOS13 (mitochondrial contact site and cristae organizing system subunit 13) [NCBI Gene 125988] {aka C19orf70, MIC12, MIC13, P117, QIL1}, CLDN6 (claudin 6) [NCBI Gene 9074], ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, WNT2 (Wnt family member 2) [NCBI Gene 7472] {aka INT1L1, IRP}
- **Diseases:** cervical cancer (MESH:D002583), NSCLC (MESH:D002289), cytotoxicity (MESH:D064420), monkeypox (MESH:D045908), pancreatic cancer (MESH:D010190), cervical intraepithelial neoplasia (MESH:D002578), parasitic disease (MESH:D010272), cardiomyopathy (MESH:D009202), colorectal cancer (MESH:D015179), placental dysfunction (MESH:D010922), AIDS (MESH:D000163), congenital malformations (OMIM:163000), infection (MESH:D007239), rabies (MESH:D011818), HIV (MESH:D015658), HPV infection (MESH:D030361), injury to (MESH:D014947), PDAC (MESH:D021441), deaths (MESH:D003643), lung cancer (MESH:D008175), melanoma lung metastasis (MESH:D009362), Malaria (MESH:D008288), influenza (MESH:D007251), Infectious Disease (MESH:D003141), HER2-positive breast cancer (MESH:D001943), inflammatory (MESH:D007249), solid (MESH:D018250), allergic reaction (MESH:D004342), genetic toxicity (MESH:D030342), COVID-19 (MESH:D000086382), melanoma (MESH:D008545), Cancer (MESH:D009369), Guillain-Barre syndrome (MESH:D020275), Zika virus (MESH:D000071243)
- **Chemicals:** m6A (MESH:C005955), adenine (MESH:D000225), N6-methyladenosine (MESH:C010223), Lipid (MESH:D008055), pseudouridine (MESH:D011560), GPI (MESH:D017261), Polymer (MESH:D011108), Cholesterol (MESH:D002784), TriMix (MESH:C045257), ipilimumab (MESH:D000074324), PAMAM (-), poly(A) (MESH:D011061), disulfide (MESH:D004220), thiol (MESH:D013438), polylysine (MESH:D011107), silica (MESH:D012822), aluminum (MESH:D000535), PEG (MESH:D011092), Atezolizumab (MESH:C000594389)
- **Species:** Homo sapiens (human, species) [taxon 9606], Lyssavirus rabies (species) [taxon 11292], H7N9 subtype (serotype) [taxon 333278], Toxoplasma gondii (species) [taxon 5811], Mus musculus (house mouse, species) [taxon 10090], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Macaca (macaque, genus) [taxon 9539], Human immunodeficiency virus 1 (no rank) [taxon 11676], Zika virus (no rank) [taxon 64320], Orthomyxoviridae (family) [taxon 11308], H1N1 subtype (serotype) [taxon 114727], H10N8 subtype (serotype) [taxon 286285], Plasmodium falciparum (malaria parasite P. falciparum, species) [taxon 5833], Canis lupus familiaris (dog, subspecies) [taxon 9615], Monkeypox virus (no rank) [taxon 10244], H3N2 subtype (serotype) [taxon 119210]
- **Mutations:** 8  C, D8, A29L, H3L, R333Q, E8L, A35R

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC13030624/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13030624/full.md

## References

136 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030624/full.md

---
Source: https://tomesphere.com/paper/PMC13030624