Evidence map›Paper›PMID 24890740›Full record

ArticleChembiochem : a European journal of chemical biology2014

Immune and anticancer responses elicited by fully synthetic aberrantly glycosylated MUC1 tripartite vaccines modified by a TLR2 or TLR9 agonist.

Abu-Baker M Abdel-Aal, Vani Lakshminarayanan, Pamela Thompson, Nitin Supekar, Judy M Bradley, Margreet A Wolfert, Peter A Cohen, Sandra J Gendler, Geert-Jan Boons

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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  10. Synthetic protein conjugate vaccines provide protection againstProceedings of the National Academy of Sciences of the United States of America · 2021
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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

9 authors.

Abu-Baker M Abdel-AalComplex Carbohydrate Research Center, University of Georgia, 315 Riverbend Road, Athens, GA 30602 (USA).
Vani Lakshminarayanan
Pamela Thompson
Nitin Supekar
Judy M Bradley
Margreet A Wolfert
Peter A Cohen
Sandra J Gendler
Geert-Jan Boons

Funding

The Role of CHFR in Tumorigenesis and Paclitaxel-Sensitivity in Breast CancerP50CA116201 · NCI · MAYO CLINIC ROCHESTER · PI PETER C LUCAS · 2005 to 2026
$49.9M
Tissue CoreP50CA102701 · NCI · MAYO CLINIC ROCHESTER · PI COHEN, PETER A · 2004 to 2018
$32.7M
Synthesis/Immunological Properties of Lewis AntigensR01CA088986 · NCI · UNIVERSITY OF GEORGIA (UGA) · PI BOONS, GEERT-JAN · 2002 to 2015
$4.6M
Role of Vav1 protooncogene in pancreatic cancerP20CA102701 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI PETERSEN, GLORIA M. · 2003 to 2003
$1.5M
NCI NIH HHS P20 CA102701NCI NIH HHS P50 CA102701NCI NIH HHS P50 CA116201NCI NIH HHS R01 CA088986NCI NIH HHS R01 CA88986
6 · The paper itself

Abstract

The mucin MUC1 is overexpressed and aberrantly glycosylated by many epithelial cancer cells manifested by truncated O-linked saccharides. Although tumor-associated MUC1 has generated considerable attention because of its potential for the development of a therapeutic cancer vaccine, it has been difficult to design constructs that consistently induce cytotoxic T-lymphocytes (CTLs) and ADCC-mediating antibodies specific for the tumor form of MUC1. We have designed, chemically synthesized, and immunologically examined vaccine candidates each composed of a glycopeptide derived from MUC1, a promiscuous Thelper peptide, and a TLR2 (Pam3 CysSK4 ) or TLR9 (CpG-ODN 1826) agonist. It was found that the Pam3 CysSK4 -containing compound elicits more potent antigenic and cellular immune responses, resulting in a therapeutic effect in a mouse model of mammary cancer. It is thus shown, for the first time, that the nature of an inbuilt adjuvant of a tripartite vaccine can significantly impact the quality of immune responses elicited against a tumor-associated glycopeptide. The unique adjuvant properties of Pam3 CysSK4 , which can reduce the suppressive function of regulatory T cells and enhance the cytotoxicity of tumor-specific CTLs, are likely responsible for the superior properties of the vaccine candidate 1.

Indexed as

Adjuvants, ImmunologicAmino Acid SequenceAnimalsBreastBreast NeoplasmsCancer VaccinesCell Line, TumorFemaleGlycopeptidesGlycosylationHumansImmunity, CellularImmunizationMiceMice, Inbred C57BLMolecular Sequence DataAdjuvants, ImmunologicCancer VaccinesGlycopeptidesMucin-1Toll-Like Receptor 2Toll-Like Receptor 9Vaccines, Syntheticadjuvantscancercarbohydratesmucinspeptidesvaccines

Identifiers

PMID24890740
PMCPMC4113397

What OpenQuestion holds

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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.