Evidence map›Paper›PMID 17376923›Full record

ArticleJournal of virology2007

Cytomegalovirus infection in Gambian infants leads to profound CD8 T-cell differentiation.

David J C Miles, Marianne van der Sande, David Jeffries, Steve Kaye, Jamila Ismaili, Olubukola Ojuola, Mariama Sanneh, Ebrima S Touray, Pauline Waight, Sarah Rowland-Jones and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

75 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Perturbation of the Preterm Human Immune System in Early Life.medRxiv : the preprint server for health sciences · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Cytomegalovirus infections in infants in Uganda: Newborn-mother pairs, neonates with sepsis, and infants with hydrocephalus.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Article
  14. Review
  15. Review
  16. Review
  17. The untwining of immunosenescence and aging.Seminars in immunopathology · 2020
    Review
  18. Article
  19. Article
  20. Article

15 more citing papers are in PubMed but not listed here.

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 6 institutions in 6 countries.

David J C MilesMRC Laboratories Gambia, P.O. Box 273, Banjul, The Gambia. djcm1@liverpool.ac.uk
Marianne van der Sande
David Jeffries
Steve Kaye
Jamila Ismaili
Olubukola Ojuola
Mariama Sanneh
Ebrima S Touray
Pauline Waight
Sarah Rowland-Jones
Hilton Whittle
Arnaud Marchant
MRC Unit the Gambia · GMBronx-Lebanon Hospital Center · USImperial College London · GBInstitut Pasteur de Lille · FRNational Institute for Public Health and the Environment · NLUniversité Libre de Bruxelles · BE

Funding

Medical Research Council MC_U190081978Medical Research Council MC_U190085854
6 · The paper itself

Abstract

Cytomegalovirus (CMV) infection is endemic in Gambian infants, with 62% infected by 3 months and 85% by 12 months of age. We studied the CD8 T-cell responses of infants to CMV following primary infection. CMV-specific CD8 T cells, identified with tetramers, showed a fully differentiated phenotype (CD28(-) CD62L(-) CD95(+) perforin(+) granzyme A(+) Bcl-2(low)). Strikingly, the overall CD8 T-cell population developed a similar phenotype following CMV infection, which persisted for at least 12 months. In contrast, primary infection was accompanied by up-regulation of markers of activation (CD45R0 and HLA-D) on both CMV-specific cells and the overall CD8 T-cell population and division (Ki-67) of specific cells, but neither pattern persisted. At 12 months of age, the CD8 T-cell population of CMV-infected infants was more differentiated than that of uninfected infants. Although the subpopulation of CMV-specific cells remained constant, the CMV peptide-specific gamma interferon response was lower in younger infants and increased with age. As the CD8 T-cell phenotype induced by CMV is indicative of immune dysfunction in the elderly, the existence of a similar phenotype in large numbers of Gambian infants raises the question of whether CMV induces a similarly deleterious effect.

Indexed as

AdultCD8-Positive T-LymphocytesCell DifferentiationCells, CulturedCross-Sectional StudiesCytomegalovirusCytomegalovirus InfectionsFemaleGambiaHumansImmunophenotypingInfantInfant, NewbornLongitudinal StudiesLymphocyte ActivationLymphocyte Count

Identifiers

PMID17376923
PMCPMC1900274
OpenAlexW1982977224

What OpenQuestion holds

Textmetadata
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.