Evidence map›Paper›PMID 38055824›Full record

ArticleScience advances2023

Innate TCRβ-chain engagement drives human T cells toward distinct memory-like effector phenotypes with immunotherapeutic potentials.

Pierre Vantourout, Josephine Eum, María Conde Poole, Thomas S Hayday, Adam G Laing, Khiyam Hussain, Rosamond Nuamah, Shichina Kannambath, Jacques Moisan, Allart Stoop and 6 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

16 authors at 4 institutions in 2 countries.

Pierre VantouroutPeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.ORCID 0000-0001-7287-5517
Josephine EumPeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.ORCID 0000-0003-4247-248X
María Conde PoolePeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.
Thomas S HaydayPeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.ORCID 0000-0003-2268-5250
Adam G LaingPeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.ORCID 0000-0003-0112-2280
Khiyam HussainPeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.
Rosamond NuamahNIHR BRC Genomics Research Platform, Guy's and St Thomas' NHS Foundation Trust, King's College London School of Medicine, Guy's Hospital, London, SE1 9RT, UK.
Shichina KannambathNIHR BRC Genomics Research Platform, Guy's and St Thomas' NHS Foundation Trust, King's College London School of Medicine, Guy's Hospital, London, SE1 9RT, UK.
Jacques MoisanMarengo Therapeutics, Cambridge, MA 02139, USA.
Allart StoopMarengo Therapeutics, Cambridge, MA 02139, USA.ORCID 0000-0001-6931-5682
Sebastiano BattagliaBridge Informatics, Salem, MA, 01970, USA.
Roya ServattalabMarengo Therapeutics, Cambridge, MA 02139, USA.
Jonathan HsuMarengo Therapeutics, Cambridge, MA 02139, USA.ORCID 0000-0001-9851-1439
Andrew BayliffeMarengo Therapeutics, Cambridge, MA 02139, USA.ORCID 0000-0002-7892-9210
Madan KatragaddaMarengo Therapeutics, Cambridge, MA 02139, USA.ORCID 0009-0004-2394-6816
Adrian C HaydayPeter Gorer Department of Immunobiology, School of Immunology and Microbial Sciences, King's College London, London, SE1 9RT, UK.ORCID 0000-0002-9495-5793
King's College London · GBIo Therapeutics (United States) · USGuy's and St Thomas' NHS Foundation Trust · GBSalem University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clonotypic αβ T cell responses to cargoes presented by major histocompatibility complex (MHC), MR1, or CD1 proteins underpin adaptive immunity. Those responses are mostly mediated by complementarity-determining region 3 motifs created by quasi-random T cell receptor (TCR) gene rearrangements, with diversity being highest for TCRγδ. Nonetheless, TCRγδ also displays nonclonotypic innate responsiveness following engagement of germline-encoded Vγ-specific residues by butyrophilin (BTN) or BTN-like (BTNL) proteins that uniquely mediate γδ T cell subset selection. We now report that nonclonotypic TCR engagement likewise induces distinct phenotypes in TCRαβ

Indexed as

Receptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-deltaButyrophilinsHumansImmunotherapyPhenotypeT-Lymphocyte SubsetsButyrophilinsReceptors, Antigen, T-Cell, alpha-betaReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID38055824
PMCPMC10699787
OpenAlexW4389383336

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.