Evidence map›Paper›PMID 31358938›Full record

ArticleBritish journal of cancer2019

Distinct prognostic value of circulating anti-telomerase CD4

Caroline Laheurte, Magalie Dosset, Dewi Vernerey, Laura Boullerot, Béatrice Gaugler, Eléonore Gravelin, Vincent Kaulek, Marion Jacquin, Laurie Cuche, Guillaume Eberst and 7 more

Abstract read
In one paragraph

Article in British journal of cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
–field-weighted citation impact
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

57 citing papers in PubMed.

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  6. Anti-Telomerase CD4International journal of molecular sciences · 2020
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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

17 authors.

Caroline LaheurteUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Magalie DossetUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Dewi VernereyUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Laura BoullerotUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Béatrice GauglerUPMC Univ Paris 06, INSERM UMR 938, Centre de Recherche Saint-Antoine, Sorbonne Universités, F-75012, Paris, France.
Eléonore GravelinUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Vincent KaulekDepartment of Pneumology, University Hospital of Besançon, F-25000, Besançon, France.
Marion JacquinINSERM CIC-1431, Clinical Investigation Center in Biotherapy, Plateforme de Biomonitoring, F-25000, Besançon, France.
Laurie CucheDepartment of Pneumology, University Hospital of Besançon, F-25000, Besançon, France.
Guillaume EberstDepartment of Pneumology, University Hospital of Besançon, F-25000, Besançon, France.
Pascale JacouletDepartment of Pneumology, University Hospital of Besançon, F-25000, Besançon, France.
Elizabeth FabreDepartment of medical Oncology, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.
Françoise Le Pimpec-BarthesDepartment of Thoracic surgery, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.
Eric TartourDepartment of Biological Immuology, Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Paris, France.
Marcelo De Carvalho BittencourtUniversity Hospital of Nancy and CECITA team, IMOPA UMR7365 University of Lorraine/CNRS, Laboratory of Immunology, Vandoeuvre-les-Nancy, France.
Virginie WesteelUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France.
Olivier AdotéviUniversity Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, F-25000, Besançon, France. olivier.adotevi@univ-fcomte.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite the critical roles of Th1-polarised CD4

methodsThe circulating antitumor Th1 response was assessed by the ELISpot assay in 170 NSCLC patients using a mixture of HLA class II-restricted peptides from telomerase (TERT). Phenotyping of blood immune cells was performed by flow cytometry.

resultsTERT-reactive CD4 T-cell response was detected in 35% of NSCLC patients before any treatment. Functional analysis showed that these cells were effector memory and Th1 polarised capable to produce effector cytokines, such as IFN-γ, TNF-α and IL-2. The presence of anti-TERT Th1 response was inversely correlated with the level of exhausted PD-1

conclusionsSystemic anti-TERT Th1 response plays a strong antitumor protective role in NSCLC. This study underlines the potential interest of monitoring circulating antitumor Th1 response for patients' stratification and therapy decision.

Indexed as

AgedCarcinoma, Non-Small-Cell LungCytokinesFemaleHepatitis A Virus Cellular Receptor 2HumansIn Vitro TechniquesLung NeoplasmsMaleMiddle AgedPrognosisProgrammed Cell Death 1 ReceptorSurvival RateTelomeraseTh1 CellsT-LymphocytesCytokinesHAVCR2 protein, humanHepatitis A Virus Cellular Receptor 2PDCD1 protein, humanProgrammed Cell Death 1 ReceptorTelomerase

Identifiers

PMID31358938
PMCPMC6738094

What OpenQuestion holds

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Registered trials

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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.