Evidence map›Paper›PMID 35802024›Full record

ArticleBritish journal of haematology2022

Chronic myeloid leukaemia patients at diagnosis and resistant to tyrosine kinase inhibitor therapy display exhausted T-cell phenotype.

Patrick Harrington, Richard Dillon, Deepti Radia, Donal McLornan, Claire Woodley, Susan Asirvatham, Kavita Raj, Natalia Curto-Garcia, Jamie Saunders, Shahram Kordasti and 2 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of haematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 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 2 institutions in 1 country.

Patrick HarringtonDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0001-5704-466X
Richard DillonDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Deepti RadiaDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-3578-0102
Donal McLornanDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-1224-091X
Claire WoodleyDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Susan AsirvathamDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Kavita RajDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Natalia Curto-GarciaDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0003-1437-4583
Jamie SaundersDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Shahram KordastiDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Claire HarrisonDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.ORCID 0000-0002-3212-920X
Hugues de LavalladeDepartment of Clinical Haematology, Guy's & St Thomas' NHS Foundation Trust, London, UK.
Guy's and St Thomas' NHS Foundation Trust · GBKing's College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The search for novel targets in chronic myeloid leukaemia (CML) is ongoing, to improve treatment efficacy in refractory disease and increase eligibility for tyrosine kinase inhibitor (TKI) discontinuation. Increased frequency of Tregs and effector Tregs was evident at diagnosis, together with increased expression of T-cell exhaustion markers, including in regulatory T cells at diagnosis and in patients with refractory disease. Plasma analysis revealed significantly increased levels of cytokines including tumour necrosis factor (TNF)-a and interleukin (IL)-6 at diagnosis, in keeping with a pro-inflammatory state prior to treatment. We hence demonstrate T-cell exhaustion and a pro-inflammatory state at diagnosis in CML, likely secondary to leukaemia-associated antigenic overload associated with increased disease burden.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveLeukemia, MyeloidHumansPhenotypeProtein Kinase InhibitorsT-Lymphocytes, RegulatoryProtein Kinase InhibitorsCMLimmune checkpointinflammationT cellT-cell exhaustionTreg

Identifiers

PMID35802024
PMCPMC9544983
OpenAlexW4284967069

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.