Evidence map›Paper›PMID 27243552›Full record

ArticleScientific reports2016

Differential effects of Cytomegalovirus carriage on the immune phenotype of middle-aged males and females.

Marieke van der Heiden, Menno C van Zelm, Sophinus J W Bartol, Lia G H de Rond, Guy A M Berbers, Annemieke M H Boots, Anne-Marie Buisman

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 60 citations in OpenAlex.

  1. Trial
  2. Trial
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  4. Article
  5. CMV-specific clonal expansion of Th1, GZMKbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. CMV infection, CD19Immunity & ageing : I & A · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. 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

7 authors at 4 institutions in 2 countries.

Marieke van der HeidenCentre for Infectious Disease Control (Cib), National Institute for Public Health and the Environment (RIVM), Bilthoven 3720 BA, The Netherlands.
Menno C van ZelmDepartment of Immunology, Erasmus MC, Rotterdam 3000 CA, The Netherlands.
Sophinus J W BartolDepartment of Immunology, Erasmus MC, Rotterdam 3000 CA, The Netherlands.
Lia G H de RondCentre for Infectious Disease Control (Cib), National Institute for Public Health and the Environment (RIVM), Bilthoven 3720 BA, The Netherlands.
Guy A M BerbersCentre for Infectious Disease Control (Cib), National Institute for Public Health and the Environment (RIVM), Bilthoven 3720 BA, The Netherlands.
Annemieke M H BootsDepartment of Rheumatology and Clinical Immunology, University of Groningen, University Medical Centre Groningen, Groningen 9700 RB, The Netherlands.
Anne-Marie BuismanCentre for Infectious Disease Control (Cib), National Institute for Public Health and the Environment (RIVM), Bilthoven 3720 BA, The Netherlands.
National Institute for Public Health and the Environment · NLErasmus University Rotterdam · NLMonash University · AUUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The elderly population is more susceptible to infections as a result of an altered immune response, commonly referred to as immunosenescence. Cytomegalovirus (CMV)-infection associated changes in blood lymphocytes are known to impact this process, but the interaction with gender remains unclear. Therefore, we analysed the effects and interaction of gender and CMV on the absolute numbers of a comprehensive set of naive and memory T- and B-cell subsets in people between 50 and 65 years of age. Enumeration and characterisation of lymphocyte subsets by flow cytometry was performed on fresh whole blood samples from 255 middle-aged persons. CMV-IgG serostatus was determined by ELISA. Gender was a major factor affecting immune cell numbers. CMV infection was mainly associated with an expansion of late-differentiated T-cell subsets. CMV+ males carried lower numbers of total CD4+, CD4+ central memory (CM) and follicular helper T-cells than females and CMV- males. Moreover, CMV+ males had significantly lower numbers of regulatory T (Treg)-cells and memory B-cells than CMV+ females. We here demonstrate an interaction between the effects of CMV infection and gender on T- and B-cells in middle-aged individuals. These differential effects on adaptive immunity between males and females may have implications for vaccination strategies at middle-age.

Indexed as

Adaptive ImmunityAgedAntibodies, ViralB-Lymphocyte SubsetsCarrier StateCytomegalovirusCytomegalovirus InfectionsFemaleHumansImmunoglobulin GImmunologic MemoryImmunophenotypingLymphocyte CountMaleMiddle AgedPhenotypeAntibodies, ViralImmunoglobulin G

Identifiers

PMID27243552
PMCPMC4886678
OpenAlexW2461330194

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.