Evidence map›Paper›PMID 32595211›Full record

ArticleBritish journal of cancer2020

An effective peptide vaccine strategy circumventing clonal MHC heterogeneity of murine myeloid leukaemia.

A-Ri Shin, Sang-Eun Lee, Haeyoun Choi, Hyun-Jung Sohn, Hyun-Il Cho, Tai-Gyu Kim

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact, top 91% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
  5. Review
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

6 authors at 2 institutions in 1 country.

A-Ri ShinDepartment of Microbiology and Immunology, College of Medicine, The Catholic University of Korea, Seoul, 06591, South Korea.
Sang-Eun LeeDepartment of Microbiology and Immunology, College of Medicine, The Catholic University of Korea, Seoul, 06591, South Korea.
Haeyoun ChoiDepartment of Microbiology and Immunology, College of Medicine, The Catholic University of Korea, Seoul, 06591, South Korea.
Hyun-Jung SohnTranslational and Clinical Division, ViGenCell Inc., Seoul, 06591, South Korea.
Hyun-Il ChoTranslational and Clinical Division, ViGenCell Inc., Seoul, 06591, South Korea. chohil@vigencell.com.ORCID http://orcid.org/0000-0002-6520-3066
Tai-Gyu KimDepartment of Microbiology and Immunology, College of Medicine, The Catholic University of Korea, Seoul, 06591, South Korea. kimtg@catholic.ac.kr.
Catholic University of Korea · KRNovaCell Technology (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTherapeutic cancer vaccines are an attractive approach for treating malignant tumours, and successful tumour eradication depends primarily on controlling tumour immunosuppression status as well as heterogeneity of tumour cells driven by epigenetic alterations.

methodsPeptide-loaded dendritic cell (DC) prime and non-infectious peptide booster heterologous immunisations were assessed for the immunogenicity of polo-like kinase-1 (PLK1)-derived peptides. Heterologous vaccination regimen targeting multiple shared tumour antigens simultaneously with PD-L1 blockade was assessed against murine myeloid leukaemia.

resultsA synthetic PLK1

conclusionsOur findings suggest that PLK1 could be an attractive immunotherapeutic target antigen for cancer immunotherapy, and that similar strategies would be applicable for the optimisation of cancer vaccines for the treatment of numerous viral diseases and malignant tumours.

Indexed as

VaccinationAnimalsAntigens, CD19Cancer VaccinesCD8-Positive T-LymphocytesCell Cycle ProteinsFemaleHistocompatibility Antigens Class IImmune Checkpoint InhibitorsLeukemia, MyeloidMiceMice, Inbred C57BLPeptide FragmentsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene ProteinsAntigens, CD19Cancer VaccinesCell Cycle ProteinsHistocompatibility Antigens Class IImmune Checkpoint InhibitorsPeptide FragmentsPolo-Like Kinase 1Protein Serine-Threonine KinasesProto-Oncogene Proteins

Identifiers

PMID32595211
PMCPMC7492404
OpenAlexW3037674310

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.