Evidence map›Paper›PMID 26595674›Full record

ArticleBioconjugate chemistry2016

Synthesis of a Liposomal MUC1 Glycopeptide-Based Immunotherapeutic and Evaluation of the Effect of l-Rhamnose Targeting on Cellular Immune Responses.

Partha Karmakar, Kyunghee Lee, Sourav Sarkar, Katherine A Wall, Steven J Sucheck

Open access · greenAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

22 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Article
  3. Stereoselective Synthesis of Sialyl LewisAngewandte Chemie (International ed. in English) · 2023
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Liposomes used as a vaccine adjuvant-delivery system: From basics to clinical immunization.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Review
  11. Article
  12. Review
  13. Nanoparticle systems for cancer vaccine.Nanomedicine (London, England) · 2019
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
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 1 institution in 1 country.

Partha KarmakarDepartment of Chemistry and Biochemistry, The University of Toledo , 2801 West Bancroft Street, Toledo, Ohio 43606, United States.
Kyunghee LeeDepartment of Medicinal and Biological Chemistry, The University of Toledo Health Science Campus , 3000 Arlington Avenue, Toledo, Ohio 43614, United States.
Sourav SarkarDepartment of Chemistry and Biochemistry, The University of Toledo , 2801 West Bancroft Street, Toledo, Ohio 43606, United States.
Katherine A WallDepartment of Medicinal and Biological Chemistry, The University of Toledo Health Science Campus , 3000 Arlington Avenue, Toledo, Ohio 43614, United States.
Steven J SucheckDepartment of Chemistry and Biochemistry, The University of Toledo , 2801 West Bancroft Street, Toledo, Ohio 43606, United States.
University of Toledo · US

Funding

Synthesis of Glycopeptide-Based Cancer Antigen VaccinesR15GM094734 · NIGMS · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI WALL, KATHERINE A · 2011 to 2015
$755k
NIGMS NIH HHS GM094734-01NIGMS NIH HHS GM094734-02NIGMS NIH HHS R15 GM094734
6 · The paper itself

Abstract

Generation of a CD8(+) response to extracellular antigen requires processing of the antigen by antigen presenting cells (APC) and cross-presentation to CD8(+) T cell receptors via MHC class I molecules. Cross-presentation is facilitated by efficient antigen uptake followed by immune-complex-mediated maturation of the APCs. We hypothesize that improved antigen uptake of a glycopeptide sequence containing a CD8(+) T cell epitope could be achieved by delivering it on a liposome surface decorated with an immune complex-targeting ligand, an l-Rhamnose (Rha) epitope. We synthesized a 20-amino-acid glycopeptide TSAPDT(GalNAc)RPAPGSTAPPAHGV from the variable number tandem repeat region of the tumor marker MUC1 containing an N-terminal azido moiety and a tumor-associated α-N-acetyl galactosamine (GalNAc) at the immunogenic DTR motif. The MUC1 antigen was attached to Pam3Cys, a Toll-like receptor-2 ligand via copper(I)-catalyzed azido-alkyne cycloaddition (CuAAc) chemistry. The Rha-decorated liposomal Pam3Cys-MUC1-Tn 4 vaccine was evaluated in groups of C57BL/6 mice. Some groups were previously immunized to generate anti-Rha antibodies. Anti-Rha antibody expressing mice that received the Rha liposomal vaccine showed higher cellular immunogenicity compared to the control group while maintaining a strong humoral response.

Indexed as

AnimalsCancer VaccinesCD8-Positive T-LymphocytesCell ProliferationChemistry Techniques, SyntheticCholesterolEpitopesFemaleImmunoconjugatesInterferon-gammaLiposomesMice, Inbred C57BLMucin-1Protein EngineeringRhamnoseVaccinesCancer VaccinesCholesterolEpitopesImmunoconjugatesInterferon-gammaLiposomesMucin-1RhamnoseVaccines

Identifiers

PMID26595674
PMCPMC4837471
OpenAlexW2258011737

What OpenQuestion holds

Textmetadata
LicenceTDM
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.