Evidence map›Paper›PMID 28940439›Full record

ArticleClinical and experimental immunology2018

Detection of ABCB5 tumour antigen-specific CD8

S Borchers, C Maβlo, C A Müller, A Tahedl, J Volkind, Y Nowak, V Umansky, J Esterlechner, M H Frank, C Ganss and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2018. 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
0.4field-weighted citation impact, top 38% 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, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. CAR-T therapy: Prospects in targeting cancer stem cells.Journal of cellular and molecular medicine · 2021
    Review
  4. Article
  5. Review
  6. 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

12 authors at 3 institutions in 3 countries.

S BorchersRHEACELL GmbH & Co. KG, Heidelberg, Germany.ORCID 0000-0003-3514-7523
C MaβloRHEACELL GmbH & Co. KG, Heidelberg, Germany.
C A MüllerTICEBA GmbH, Heidelberg, Germany.
A TahedlTICEBA GmbH, Heidelberg, Germany.
J VolkindTICEBA GmbH, Heidelberg, Germany.
Y NowakSkin Cancer Unit, German Cancer Research Center (DKFZ) and Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Mannheim, Germany.
V UmanskySkin Cancer Unit, German Cancer Research Center (DKFZ) and Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Mannheim, Germany.
J EsterlechnerTICEBA GmbH, Heidelberg, Germany.
M H FrankTransplant Research Program, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
C GanssRHEACELL GmbH & Co. KG, Heidelberg, Germany.
M A KluthRHEACELL GmbH & Co. KG, Heidelberg, Germany.
J UtikalSkin Cancer Unit, German Cancer Research Center (DKFZ) and Department of Dermatology, Venereology and Allergology, University Medical Center Mannheim, Ruprecht-Karl University of Heidelberg, Mannheim, Germany.
Rheacell (Germany) · DEGerman Cancer Research Center · DEEdith Cowan University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ATP binding cassette subfamily B member 5 (ABCB5) has been identified as a tumour-initiating cell marker and is expressed in various malignancies, including melanoma. Moreover, treatment with anti-ABCB5 monoclonal antibodies has been shown to inhibit tumour growth in xenotransplantation models. Therefore, ABCB5 represents a potential target for cancer immunotherapy. However, cellular immune responses against ABCB5 in humans have not been described so far. Here, we investigated whether ABCB5-reactive T cells are present in human melanoma patients and tested the applicability of ABCB5-derived peptides for experimental induction of human T cell responses. Peripheral blood mononuclear cells (PBMNC) isolated from blood samples of melanoma patients (n = 40) were stimulated with ABCB5 peptides, followed by intracellular cytokine staining (ICS) for interferon (IFN)-γ and tumour necrosis factor (TNF)-α. To evaluate immunogenicity of ABCB5 peptides in naive healthy donors, CD8 T cells were co-cultured with ABCB5 antigen-loaded autologous dendritic cells (DC). ABCB5 reactivity in expanded T cells was assessed similarly by ICS. ABCB5-reactive CD8

Indexed as

Amino Acid SequenceAntigens, NeoplasmATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 1CD8-Positive T-LymphocytesCytokinesCytotoxicity, ImmunologicDendritic CellsEpitopes, T-LymphocyteFemaleHumansImmunotherapyLymphocyte ActivationMaleMelanomaNeoplasm StagingABCB5 protein, humanAntigens, NeoplasmATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 1CytokinesEpitopes, T-LymphocytePeptidesABCB5immunotherapymelanomatumour-specific T cells

Identifiers

PMID28940439
PMCPMC5721238
OpenAlexW2756808812

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.