Evidence map›Paper›PMID 36203181›Full record

ArticleJournal of neuroinflammation2022

T-cells in human trigeminal ganglia express canonical tissue-resident memory T-cell markers.

Peter-Paul A Unger, Anna E Oja, Tamana Khemai-Mehraban, Werner J D Ouwendijk, Pleun Hombrink, Georges M G M Verjans

Open access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 23 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

6 authors at 3 institutions in 1 country.

Peter-Paul A UngerDepartment of Viroscience, Erasmus MC, Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Anna E OjaDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Tamana Khemai-MehrabanDepartment of Viroscience, Erasmus MC, Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Werner J D OuwendijkDepartment of Viroscience, Erasmus MC, Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Pleun HombrinkDepartment of Hematopoiesis, Sanquin Research and Landsteiner Laboratory, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Georges M G M VerjansDepartment of Viroscience, Erasmus MC, Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands. g.verjans@erasmusmc.nl.
Erasmus University Rotterdam · NLSanquin · NLUniversity of Amsterdam · NL

Funding

Large Scale T Cell Epitope Discovery: Local and Systemic T cell Response to Herpes Simplex Virus75N93019C00063 · NIAID · UNIVERSITY OF WASHINGTON · PI MYER, TIM · 2019 to 2023
$5.5M
Dutch MS Research Foundation 17-955 MSNIAID NIH HHS 75N93019C00063
6 · The paper itself

Abstract

backgroundTrigeminal ganglia (TG) neurons are the main site of lifelong latent herpes simplex virus type 1 (HSV-1) infection. T-cells in ganglia contribute to long-term control of latent HSV-1 infection, but it is unclear whether these cells are bona fide tissue-resident memory T-cells (T

methodsPeripheral blood mononuclear cells (PBMC; 5 blood donors) were incubated with several commercial tissue digestion enzyme preparations to determine off-target effect on simultaneous detection of 15 specific T-cell subset markers by flow cytometry. Next, optimized enzymatic digestion was applied to ex vivo phenotype T-cells in paired PBMC, normal appearing white matter (NAWM) and TG of 8 deceased brain donors obtained < 9 h post-mortem by flow cytometry. Finally, the phenotypic and functional markers, and spatial orientation of T-cells in relation to neuronal somata, were determined in TG tissue sections of five HSV-1-latently infected individuals by multiparametric in situ analysis.

resultsCollagenase IV digestion of human nervous tissue was most optimal to obtain high numbers of viable T-cells without disrupting marker surface expression. Compared to blood, majority T-cells in paired NAWM and TG were effector memory T-cells expressing the canonical T

conclusionsThe human TG represents an immunocompetent environment in which both CD4 and CD8 T

Indexed as

Herpes SimplexHerpesviridae InfectionsHerpesvirus 1, HumanCD8-Positive T-LymphocytesHumansKi-67 AntigenLeukocyte Common AntigensLeukocytes, MononuclearMemory T CellsProgrammed Cell Death 1 ReceptorTrigeminal GanglionKi-67 AntigenLeukocyte Common AntigensProgrammed Cell Death 1 ReceptorHumanNormal-appearing white matterTissue-resident memory T-cells and herpes simplex virusTrigeminal ganglion

Identifiers

PMID36203181
PMCPMC9535861
OpenAlexW4302292979

What OpenQuestion holds

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LicenceCC BY
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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.