Evidence map›Paper›PMID 18253733›Full record

ArticleCancer immunology, immunotherapy : CII2008

Recognition of naturally processed and ovarian cancer reactive CD8+ T cell epitopes within a promiscuous HLA class II T-helper region of NY-ESO-1.

Junko Matsuzaki, Feng Qian, Immanuel Luescher, Shashikant Lele, Gerd Ritter, Protul A Shrikant, Sacha Gnjatic, Lloyd J Old, Kunle Odunsi

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. A rare population of tumor antigen-specific CD4Journal for immunotherapy of cancer · 2019
    Article
  7. Review
  8. Article
  9. New Approaches for Immune Directed Treatment for Ovarian Cancer.Current treatment options in oncology · 2016
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Cellular immunotherapy for ovarian cancer.Expert opinion on biological therapy · 2009
    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

9 authors at 4 institutions in 2 countries.

Junko MatsuzakiDepartment of Gynecologic Oncology, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY 14263, USA.
Feng Qian
Immanuel Luescher
Shashikant Lele
Gerd Ritter
Protul A Shrikant
Sacha Gnjatic
Lloyd J Old
Kunle Odunsi
Roswell Park Comprehensive Cancer Center · USMemorial Sloan Kettering Cancer Center · USLudwig Cancer Research · CHLudwig Cancer Research · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

NY-ESO-1 is frequently expressed in epithelial ovarian cancer (EOC) and elicits spontaneous humoral and cellular immune responses in a proportion of EOC patients. The identification of NY-ESO-1 peptide epitopes with dual HLA-class I and class II specificities might be useful in vaccination strategies for generating cognate CD4+ T cell help to augment CD8+ T cell responses. Here, we describe two novel NY-ESO-1-derived MHC class I epitopes from EOC patients with spontaneous humoral immune response to NY-ESO-1. CD8+ T cells derived from NY-ESO-1 seropositive EOC patients were presensitized with a recombinant adenovirus encoding NY-ESO-1or pooled overlapping peptides. These epitopes, ESO127-136 presented by HLA-A68 molecule, and ESO127-135 restricted by HLA-Cw15 allele, are located within ESO119-143, a promiscuous HLA-class II region containing epitopes that bind to multiple HLA-DR alleles. The novel epitopes were naturally processed by APC or naturally presented by tumor cell lines. In addition, these epitopes induced NY-ESO-1-specific CTL in NY-ESO-1 seropositive EOC patients. Together, the results indicate that ESO119-143 epitope has dual HLA classes I and II specificities, and represents a potential vaccine candidate in a large number of cancer patients.

Indexed as

Antigen PresentationCD8-Positive T-LymphocytesCell Line, TumorEpitopes, T-LymphocyteFemaleFlow CytometryHistocompatibility Antigens Class IHistocompatibility Antigens Class IIHumansOvarian NeoplasmsSensitivity and SpecificityT-Lymphocytes, Helper-InducerEpitopes, T-LymphocyteHistocompatibility Antigens Class IHistocompatibility Antigens Class II

Identifiers

PMID18253733
PMCPMC11031114
OpenAlexW2036949530

What OpenQuestion holds

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Registered trials

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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.