Evidence map›Paper›PMID 28934430›Full record

ArticleThe Journal of infectious diseases2017

Epstein-Barr Virus Type 2 Infects T Cells in Healthy Kenyan Children.

Carrie B Coleman, Ibrahim I Daud, Sidney O Ogolla, Julie A Ritchie, Nicholas A Smith, Peter O Sumba, Arlene E Dent, Rosemary Rochford

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

  1. EBV Genome Variations and Association With Diseases.Journal of medical virology · 2026
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  8. Article
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  10. Article
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  12. Observational
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  16. [Research status of Epstein Barr virus in children with adenotonsillar hypertrophy].Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology head and neck surgery · 2021
    Review
  17. Review
  18. Article
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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

8 authors.

Carrie B ColemanDepartment of Immunology and Microbiology, University of Colorado-Denver School of Medicine, Aurora.
Ibrahim I DaudAcademic Model Providing Access to Healthcare Research Laboratories, Eldoret, Kenya.
Sidney O OgollaDepartment of Immunology and Microbiology, University of Colorado-Denver School of Medicine, Aurora.
Julie A RitchieDepartment of Microbiology and Immunology, SUNY Upstate Medical University, Syracuse, New York.
Nicholas A SmithDepartment of Immunology and Microbiology, University of Colorado-Denver School of Medicine, Aurora.
Peter O SumbaCenter for Global Health Research, Kenya Medical Research Institute, Kisumu.
Arlene E DentCenter for Global Health and Diseases, Case Western Reserve University, Cleveland, Ohio.
Rosemary RochfordDepartment of Immunology and Microbiology, University of Colorado-Denver School of Medicine, Aurora.

Funding

TRAINING PROGRAM IN IMMUNOLOGYT32AI007405 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Laurel L Lenz, Raul Martin Torres · 1991 to 2026
$10.5M
NIAID NIH HHS T32 AI007405
6 · The paper itself

Abstract

Background: The 2 strains of Epstein-Barr virus (EBV), EBV type 1 (EBV-1) and EBV-2, differ in latency genes, suggesting that they use distinct mechanisms to establish latency. We previously reported that EBV-2 infects T cells in vitro. In this study, we tested the possibility that EBV-2 infects T cells in vivo. Methods: Purified T-cell fractions isolated from children positive for EBV-1 or EBV-2 and their mothers were examined for the presence of EBV and for EBV type. Results: We detected EBV-2 in all T-cell samples obtained from EBV-2-infected children at 12 months of age, with some children retaining EBV-2-positive T cells through 24 months of age, suggesting that EBV-2 persists in T cells. We were unable to detect EBV-2 in T-cell samples from mothers but could detect EBV-2 in samples of their breast milk and saliva. Conclusions: These data suggest that EBV-2 uses T cells as an additional latency reservoir but that, over time, the frequency of infected T cells may drop below detectable levels. Alternatively, EBV-2 may establish a prolonged transient infection in the T-cell compartment. Collectively, these novel findings demonstrate that EBV-2 infects T cells in vivo and suggest EBV-2 may use the T-cell compartment to establish latency.

Indexed as

Child, PreschoolCohort StudiesDNA, ViralEpstein-Barr Virus InfectionsFemaleHerpesvirus 4, HumanHumansInfantKenyaMaleMilk, HumanPrevalenceSalivaSpecimen HandlingT-LymphocytesVirus LatencyDNA, ViralBurkitt lymphomacellular tropismEpstein-Barr virusT lymphocytes

Identifiers

PMID28934430
PMCPMC5853903

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.