Evidence map›Paper›PMID 42256613›Full record

ReviewRSC pharmaceutics2026

Nanoparticle vaccine formulations for dengue virus.

Connor T Murphy, Kristy M Ainslie

Abstract readReview
In one paragraph

Review in RSC pharmaceutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Connor T MurphyDivision of Pharmacoengineering & Molecular Pharmaceutics, Eshelman School of Pharmacy, UNC 4012 Marsico Hall 125 Mason Farm Road Chapel Hill NC 27599 USA ainsliek@email.unc.edu.
Kristy M AinslieDivision of Pharmacoengineering & Molecular Pharmaceutics, Eshelman School of Pharmacy, UNC 4012 Marsico Hall 125 Mason Farm Road Chapel Hill NC 27599 USA ainsliek@email.unc.edu.ORCID https://orcid.org/0000-0002-1820-8382

Funding

Mechanistic evaluation of mast cell agonists combined with TLR, NOD and STING agonists.R01AI167099 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Kristy M Ainslie · 2023 to 2026
$2.5M
NIAID NIH HHS R01 AI167099
6 · The paper itself

Abstract

Dengue virus (DENV) is one of the most prevalent mosquito-borne pathogens, with almost half of the global population at risk of infection. While most cases are mild, severe illness and even death is not uncommon. There are currently a lack of available antivirals and highly effective prophylactic vaccines available for DENV, leading to a significant gap in protection. While live-attenuated vaccines have been developed and briefly utilized, some have been found to increase the risk for developing antibody-dependent enhancement (ADE), a phenomenon that can worsen outcomes in those who are exposed to DENV after receiving the vaccination. Nanoparticle-based vaccine formulations provide numerous advantages over live-attenuated vaccines such as controlled release, dose-sparing, and ability to effectively encapsulate adjuvants and viral antigens, while simultaneously minimizing the risk for development of ADE. Numerous carrier systems have been developed, including polymeric, lipid, inorganic, and protein-based formulations. Each system has been found to induce unique antigen-specific immune activation that includes varying degrees of humoral and cellular immune responses. While there is still much research to be done, nanoparticle-based vaccine formulations offer a promising approach to combat the growing threat of DENV.

Identifiers

PMID42256613
PMCPMC13238229

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.