Evidence map›Paper›PMID 29131157›Full record

ArticleNature medicine2017

Targeting the T cell receptor β-chain constant region for immunotherapy of T cell malignancies.

Paul M Maciocia, Patrycja A Wawrzyniecka, Brian Philip, Ida Ricciardelli, Ayse U Akarca, Shimobi C Onuoha, Mateusz Legut, David K Cole, Andrew K Sewell, Giuseppe Gritti and 6 more

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Nature medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 172 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
172citing papers in PubMed, 1 pooled it
9.7field-weighted citation impact, top 1% 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

172 citing papers in PubMed, 1 synthesis or guideline pooled it, 276 citations in OpenAlex.

  1. Advances and Perspectives in the Treatment of T-PLL.Current hematologic malignancy reports · 2020
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112 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 4 countries.

Paul M MaciociaCancer Institute, University College London, London, UK.
Patrycja A WawrzynieckaCancer Institute, University College London, London, UK.
Brian PhilipCancer Institute, University College London, London, UK.
Ida RicciardelliInstitute of Child Health, University College London, London, UK.
Ayse U AkarcaCancer Institute, University College London, London, UK.
Shimobi C OnuohaAutolus, Ltd., London, UK.
Mateusz LegutDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
David K ColeDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.
Andrew K SewellDivision of Infection and Immunity, Cardiff University School of Medicine, Cardiff, UK.ORCID http://orcid.org/0000-0003-3194-3135
Giuseppe GrittiHematology and Bone Marrow Transplant Units, Papa Giovanni XXIII Hospital, Bergamo, Italy.
Joan SomjaDepartment of Anatomy and Cellular Pathology, University of Liège, Liège, Belgium.
Miguel A PirisDepartment of Pathology, Fundación Jiménez Díaz, Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain.
Karl S PeggsCancer Institute, University College London, London, UK.
David C LinchCancer Institute, University College London, London, UK.
Teresa MarafiotiCancer Institute, University College London, London, UK.
Martin A PuleCancer Institute, University College London, London, UK.ORCID http://orcid.org/0000-0002-8347-9867
University College London · GBCardiff University · GBAutolus (United Kingdom) · GBCentro de Investigación Biomédica en Red de Cáncer · ESOspedale Papa Giovanni XXIII · ITUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mature T cell cancers are typically aggressive, treatment resistant and associated with poor prognosis. Clinical application of immunotherapeutic approaches has been limited by a lack of target antigens that discriminate malignant from healthy (normal) T cells. Unlike B cell depletion, pan-T cell aplasia is prohibitively toxic. We report a new targeting strategy based on the mutually exclusive expression of T cell receptor β-chain constant domains 1 and 2 (TRBC1 and TRBC2). We identify an antibody with unique TRBC1 specificity and use it to demonstrate that normal and virus-specific T cell populations contain both TRBC1

Indexed as

AnimalsAntineoplastic Agents, ImmunologicalCells, CulturedHEK293 CellsHumansImmunotherapy, AdoptiveJurkat CellsK562 CellsLeukemia, T-CellMaleMiceMolecular Targeted TherapyReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesAntineoplastic Agents, ImmunologicalReceptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID29131157
OpenAlexW2767453057

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.