Evidence map›Paper›PMID 27830183›Full record

ArticleTransplantation direct2016

Human Cytomegalovirus Infection Enhances NK Cell Activity In Vitro.

Astrid Tschan-Plessl, Martin Stern, Laurent Schmied, Christelle Retière, Hans H Hirsch, Christian Garzoni, Christian van Delden, Katia Boggian, Nicolas J Mueller, Christoph Berger and 4 more

Abstract read
In one paragraph

Article in Transplantation direct, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Natural Killer Cell Education in Women With Recurrent Pregnancy Loss.American journal of reproductive immunology (New York, N.Y. : 1989) · 2025
    Article
  2. The effect of COVID-19 and sex differences on natural killer cell cytotoxicity.Frontiers in cellular and infection microbiology · 2025
    Article
  3. Review
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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

14 authors.

Astrid Tschan-PlesslDepartment of Hematology, University Hospital Basel, Switzerland.; Department of Biomedicine, University Hospital Basel, Switzerland.
Martin SternDepartment of Hematology, University Hospital Basel, Switzerland.; Department of Biomedicine, University Hospital Basel, Switzerland.
Laurent SchmiedDepartment of Biomedicine, University Hospital Basel, Switzerland.
Christelle RetièreEtablissement Français du Sang and Equipe d'Accueil 4271, ImmunoVirologie et Polymorphisme Génétique, Université de Nantes, France.
Hans H HirschInfectious Diseases and Hospital Epidemiology, University Hospital Basel, Switzerland.
Christian GarzoniDepartment of Infectious Diseases, Inselspital, Bern University Hospital and University of Bern, Switzerland and Department of Internal Medicine and Infectious Diseases, Clinica Luganese, Switzerland.
Christian van DeldenService of Infectious Diseases, University Hospital Geneva, Switzerland.
Katia BoggianDivision of Infectious Diseases and Hospital Hygiene, Kantonsspital St. Gallen, Switzerland.
Nicolas J MuellerDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Switzerland.
Christoph BergerDivision of Infectious Diseases and Hospital Epidemiology, University Children's Hospital, Zurich, Switzerland.
Jean VillardTransplant Immunology Unit, Division of Immunology and Allergy, University Hospital Geneva, Switzerland.
Oriol ManuelInfectious Diseases Service and Transplantation Center, University Hospital and University of Lausanne, Switzerland.
Pascal MeylanInfectious Diseases Service and Institute of Microbiology, University Hospital and University of Lausanne, Switzerland.
Grzegorz TerszowskiDepartment of Biomedicine, University Hospital Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOccurring frequently after solid organ and hematopoietic stem cell transplantation, cytomegalovirus (CMV) replication remains a relevant cause of mortality and morbidity in affected patients. Despite these adverse effects, an increased alloreactivity of natural killer (NK) cells after CMV infection has been assumed, but the underlying physiopathological mechanisms have remained elusive.

methodsWe used serial analyses of NK cells before and after CMV infection in kidney transplant recipients as an in vivo model for CMV primary infection to explore the imprint of CMV infection using every patient as their own control: We analyzed NK cell phenotype and function in 47 CMV seronegative recipients of CMV seropositive kidney grafts, who developed CMV primary infection posttransplant. Seronegative recipients of seronegative kidney grafts served as controls.

resultsWe observed a significant increase of NKG2C expressing NK cells after CMV infection (mean increase, 17.5%; 95% confidence interval [95% CI], 10.2-24.9,

conclusionsWe report evidence for an increased function of NK cells induced by CMV infection. This increased in vitro functionality was seen in NKG2C-positive and NKG2C-negative subsets, arguing for an NKG2C independent mechanism of action.

Identifiers

PMID27830183
PMCPMC5087575

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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.