Evidence map›Paper›PMID 26784514›Full record

ArticlePloS one2016

Identification of Novel HLA-A*24:02-Restricted Epitope Derived from a Homeobox Protein Expressed in Hematological Malignancies.

Maiko Matsushita, Yohei Otsuka, Naoya Tsutsumida, Chiaki Tanaka, Akane Uchiumi, Koji Ozawa, Takuma Suzuki, Daiju Ichikawa, Hiroyuki Aburatani, Shinichiro Okamoto and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Maiko MatsushitaDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Yohei OtsukaDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Naoya TsutsumidaDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Chiaki TanakaDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Akane UchiumiDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Koji OzawaDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Takuma SuzukiDivision of Pharmacy, National Cancer Center Hospital, Tokyo, Japan.
Daiju IchikawaDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Hiroyuki AburataniGenome Science Laboratory Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Shinichiro OkamotoDivision of Hematology, Keio University, School of Medicine, Tokyo, Japan.
Yutaka KawakamiDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University, School of Medicine, Tokyo, Japan.
Yutaka HattoriDivision of Clinical Physiology and Therapeutics, Keio University, Faculty of Pharmacy, Tokyo, Japan.
Keio University · JPThe University of Tokyo · JPTokyo National Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The homeobox protein, PEPP2 (RHOXF2), has been suggested as a cancer/testis (CT) antigen based on its expression pattern. However, the peptide epitope of PEPP2 that is recognized by cytotoxic T cells (CTLs) is unknown. In this study, we revealed that PEPP2 gene was highly expressed in myeloid leukemia cells and some other hematological malignancies. This gene was also expressed in leukemic stem-like cells. We next identified the first reported epitope peptide (PEPP2(271-279)). The CTLs induced by PEPP2(271-279) recognized PEPP2-positive target cells in an HLA-A*24:02-restricted manner. We also found that a demethylating agent, 5-aza-2'-deoxycytidine, could enhance PEPP2 expression in leukemia cells but not in blood mononuclear cells from healthy donors. The cytotoxic activity of anti-PEPP2 CTL against leukemic cells treated with 5-aza-2'-deoxycytidine was higher than that directed against untreated cells. These results suggest a clinical rationale that combined treatment with this novel antigen-specific immunotherapy together with demethylating agents might be effective in therapy-resistant myeloid leukemia patients.

Indexed as

AzacitidineCase-Control StudiesCell Line, TumorCells, CulturedDecitabineEpitopesHLA-A24 AntigenHomeodomain ProteinsHumansLeukemia, MyeloidMonocytesNeoplastic Stem CellsT-Lymphocytes, CytotoxicAzacitidineDecitabineEpitopesHLA-A*24:02 antigenHLA-A24 AntigenHomeodomain ProteinsRHOXF2 protein, human

Identifiers

PMID26784514
PMCPMC4718592
OpenAlexW2398545747

What OpenQuestion holds

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LicenceCC BY
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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.