Evidence map›Paper›PMID 30200528›Full record

ArticleMolecules (Basel, Switzerland)2018

Immunogenicity of a Tripartite Cell Penetrating Peptide Containing a MUC1 Variable Number of Tandem Repeat (VNTR) and A T Helper Epitope.

Nicole Brooks, Jennifer Hsu, Sandra Esparon, Dodie Pouniotis, Geoffrey A Pietersz

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  3. Cell-penetrating peptides enhance peptide vaccine accumulation and persistence in lymph nodes to drive immunogenicity.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  4. Review
  5. Review
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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

5 authors at 4 institutions in 1 country.

Nicole BrooksSchool of Medical Sciences, RMIT University, Plenty Road, Bundoora 3083, Victoria, Australia. backupburnet@gmail.com.
Jennifer HsuBio-Organic and Medicinal Chemistry Laboratory, Burnet Institute, 85 Commercial Rd, Melbourne 3004, Australia. j.hsu@sydney.edu.au.
Sandra EsparonBio-Organic and Medicinal Chemistry Laboratory, Burnet Institute, 85 Commercial Rd, Melbourne 3004, Australia. sesparon@burnet.edu.au.
Dodie PouniotisSchool of Medical Sciences, RMIT University, Plenty Road, Bundoora 3083, Victoria, Australia. dodie.pouniotis@rmit.edu.au.
Geoffrey A PieterszBio-Organic and Medicinal Chemistry Laboratory, Burnet Institute, 85 Commercial Rd, Melbourne 3004, Australia. geoff.pietersz@burnet.edu.au.
RMIT University · AUBurnet Institute · AUMonash University · AURoyal Prince Alfred Hospital · AU

Funding

Cancer Council Victoria N/ASusan G. Komen for the Cure BCTR0600499
6 · The paper itself

Abstract

Peptide-based vaccines for cancer have many advantages however, for optimization these immunogens should incorporate peptide epitopes that induce CD8, as well as CD4 responses, antibody and long term immunity. Cell penetrating peptides (CPP) with a capacity of cytosolic delivery have been used to deliver antigenic peptides and proteins to antigen presenting cells to induce cytotoxic T cell, helper T cell and humoral responses in mice. For this study, a tripartite CPP including a mucin 1 (MUC1) variable number of tandem repeat (VNTR) containing multiple T cell epitopes and tetanus toxoid universal T helper epitope peptide (tetCD4) was synthesised (AntpMAPMUC1tet) and immune responses investigated in mice. Mice vaccinated with AntpMAPMUC1tet + CpG show enhanced antigen-specific interferon-gamma (IFN-γ) and IL-4 T cell responses compared with AntpMAPMUC1tet vaccination alone and induced a Th1 response, characterised by a higher ratio of IgG2a antibody/IgG1 antibodies. Furthermore, vaccination generated long term MUC1-specific antibody and T cell responses and delayed growth of MUC1

Indexed as

Amino Acid SequenceAnimalsAntibody SpecificityAntigen-Presenting CellsBone Marrow CellsCell DifferentiationCell-Penetrating PeptidesCytotoxicity, ImmunologicDendritic CellsEndocytosisEpitopesEpitopes, T-LymphocyteFemaleHLA-A2 AntigenImmunity, CellularImmunizationCell-Penetrating PeptidesCPG-oligonucleotideEpitopesEpitopes, T-LymphocyteHLA-A2 AntigenInterferon-gammaInterleukin-4Mucin-1OligodeoxyribonucleotidesTetanus Toxinantigen deliveryimmunogenicityimmunotherapymembrane penetrating peptidemembrane translocating peptideMucin 1multiple antigen peptidepenetratinTLR agonistvaccine

Identifiers

PMID30200528
PMCPMC6225367
OpenAlexW2889460602

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.