Evidence map›Paper›PMID 41624423›Full record

ArticleNeuro-oncology advances

T-cell receptor sequencing for detection of Epstein-Barr and cytomegalovirus-specific immune responses in glioma patients: An exploratory study.

Anna E Coghill, Nathan Van Bibber, Sean Yoder, Sepideh Mokhtari, Sugriva Forsyth, George Blanck, Kathleen M Egan

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Anna E CoghillCenter for Immunization and Infection Research in Cancer, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.ORCID https://orcid.org/0000-0001-7142-7499
Nathan Van BibberCancer Epidemiology Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
Sean YoderMolecular Genomics Core, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
Sepideh MokhtariDepartment of Neurooncology, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
Sugriva ForsythCancer Epidemiology Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.
George BlanckDepartment of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, Florida.
Kathleen M EganCancer Epidemiology Program, H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Specific herpesviruses have been implicated in glioma development. We undertook a pilot study to examine whether herpesviruses-specific human T-cell receptor (TCR) sequences in patient blood samples associate with glioma grade and survival. Methods: The study was based on 56 pretreatment blood samples collected from both patients with glioblastoma ( Results: Blood samples yielded large numbers of productive rearrangements (ie CDR3 sequences resulting in functional T-cell immunity), and one or more sequences targeting CMV and EBV were found in every patient sample. For both EBV and CMV, we observed a greater breadth (higher average number of unique CDR3 sequences) and intensity (higher average sum of all CDR3 sequences) of antiviral T-cell response in patients with lower-grade gliomas compared with glioblastoma, even after adjustment for patient age and sex in multivariate regression models. Conclusions: Interrogation of blood samples for CDR3 sequences describing the human TCR repertoire offers a novel tool for investigating anti-viral immune response in glioma. More robust immunity to herpesviruses could result in cross-reactive, primed cyto-toxic immune responses that potentially suppress development of more aggressive tumors.

Indexed as

cytomegalovirusEpstein-Barr virusgliomaherpesvirusesT-cell immunity

Identifiers

PMID41624423
PMCPMC12859700

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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.