Evidence map›Paper›PMID 15449037›Full record

ArticleCancer immunology, immunotherapy : CII2005

Peptide immunisation of HLA-DR-transgenic mice permits the identification of a novel HLA-DRbeta1*0101- and HLA-DRbeta1*0401-restricted epitope from p53.

José Manuel Rojas, Stephanie E B McArdle, Roger B V Horton, Matthew Bell, Shahid Mian, Geng Li, Selman A Ali, Robert C Rees

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Clinical and Immunological Effects of p53-Targeting Vaccines.Frontiers in cell and developmental biology · 2021
    Review
  4. Article
  5. Article
  6. Article
  7. Article
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  11. Article
  12. Article
  13. Review
  14. Immunotherapy of renal cell carcinoma.Cancer immunology, immunotherapy : CII · 2007
    Review
  15. 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

8 authors at 2 institutions in 1 country.

José Manuel RojasSchool of Sciences, The Nottingham Trent University, Clifton Lane, Nottingham, NG11 8NS, UK.
Stephanie E B McArdle
Roger B V Horton
Matthew Bell
Shahid Mian
Geng Li
Selman A Ali
Robert C Rees
Nottingham Trent University · GBUniversity of Liverpool · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Because of the central role of CD4(+) T cells in antitumour immunity, the identification of the MHC class II-restricted peptides to which CD4(+) T cells respond has become a priority of tumour immunologists. Here, we describe a strategy permitting us to rapidly determine the immunogenicity of candidate HLA-DR-restricted peptides using peptide immunisation of HLA-DR-transgenic mice, followed by assessment of the response in vitro. This strategy was successfully applied to the reported haemaglutinin influenza peptide HA(307-319), and then extended to three candidate HLA-DR-restricted p53 peptides predicted by the evidence-based algorithm SYFPEITHI to bind to HLA-DRbeta1*0101 (HLA-DR1) and HLA-DRbeta1*0401 (HLA-DR4) molecules. One of these peptides, p53(108-122), consistently induced responses in HLA-DR1- and in HLA-DR4-transgenic mice. Moreover, this peptide was naturally processed by dendritic cells (DCs), and induced specific proliferation in the splenocytes of mice immunised with p53 cDNA, demonstrating that immune responses could be naturally mounted to the peptide. Furthermore, p53(108-122) peptide was also immunogenic in HLA-DR1 and HLA-DR4 healthy donors. Thus, the use of this transgenic model permitted the identification of a novel HLA-DR-restricted epitope from p53 and constitutes an attractive approach for the rapid identification of novel immunogenic MHC class II-restricted peptides from tumour antigens, which can ultimately be incorporated in immunotherapeutic protocols.

Indexed as

Immunologic TechniquesAgedAnimalsAntigen PresentationBlotting, WesternBone Marrow CellsCD4-Positive T-LymphocytesCell ProliferationCytokinesDendritic CellsEnzyme-Linked Immunosorbent AssayEpitopesHLA-A AntigensHLA-DR AntigensHLA-DRB1 ChainsHumansCytokinesEpitopesHLA-A AntigensHLA-DR AntigensHLA-DRB1*01:01 antigenHLA-DRB1 ChainsPeptidesTumor Suppressor Protein p53

Identifiers

PMID15449037
PMCPMC11033034
OpenAlexW1981936553

What OpenQuestion holds

Textmetadata
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.