ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025
Balancing Antigen Loading on Gold Nanoparticles: Implications for Future Cancer Vaccine Strategies.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- A p53 peptide mucosal vaccine induces cellular and humoral immunity and anti-tumor effects in a murine colorectal cancer model.Cancer gene therapy · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
Abstract
Mucin 1 (MUC1) is a promising antigen for cancer vaccine development, but its low immunogenicity poses a major challenge. In this study, we have investigated the effect of varying the surface density of an artificial MUC1 glycopeptide on gold nanoparticles by co-loading them with an ovalbumin-derived peptide. Our results show that reducing the density of the MUC1 antigen on the nanoparticles does not affect the elicited immune response, as high IgG antibody levels were observed in the immunized mice, which were comparable to those obtained with higher antigen loading. These antibodies effectively reacted with natural MUC1 expressed on breast cancer cells, promoted antibody-dependent cell-mediated cytotoxicity and specifically recognized cancer tissue in immunohistochemical assays. This work could form the basis for the development of AuNP-based multicomponent vaccines that will allow the incorporation of additional immunostimulatory or complementary antigens in the future without compromising the efficacy of the MUC1 antigen.
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Registered trials
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.