Evidence map›Paper›PMID 37465673›Full record

ArticleFrontiers in immunology2023

Prediction of herpes virus infections after solid organ transplantation: a prospective study of immune function.

Dina Leth Møller, Søren Schwartz Sørensen, Omid Rezahosseini, Daniel Bräuner Rasmussen, Nicoline Stender Arentoft, Josefine Amalie Loft, Michael Perch, Finn Gustafsson, Jens Lundgren, Thomas Scheike and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Special Issue "Viral Infections and Host Immune Responses".International journal of molecular sciences · 2025
    Article
  3. Article
  4. Transplant international : official journal of the European Society for Organ Transplantation · 2025
    Article
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 at 2 institutions in 1 country.

Dina Leth MøllerViro-immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Søren Schwartz SørensenDepartment of Nephrology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Omid RezahosseiniViro-immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Daniel Bräuner RasmussenViro-immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Nicoline Stender ArentoftViro-immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Josefine Amalie LoftViro-immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Michael PerchDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Finn GustafssonDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Jens LundgrenDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Thomas ScheikeDepartment of Biostatistics, University of Copenhagen, Copenhagen, Denmark.
Jenny Dahl KnudsenDepartment of Clinical Microbiology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Sisse Rye OstrowskiDepartment of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark.
Allan RasmussenDepartment of Surgical Gastroenterology and Transplantation, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Susanne Dam NielsenViro-immunology Research Unit, Department of Infectious Diseases 8632, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKRigshospitalet · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Herpes virus infections are a major concern after solid organ transplantation and linked to the immune function of the recipient. We aimed to determine the incidence of positive herpes virus (cytomegalovirus (CMV), Epstein-Barr virus (EBV), herpes simplex virus type 1/2 (HSV-1/2), and varicella zoster virus (VZV)) PCR tests during the first year post-transplantation and assess whether a model including immune function pre-transplantation and three months post-transplantation could predict a subsequent positive herpes virus PCR. Methods: All participants were preemptively screened for CMV, and EBV IgG-negative participants were screened for EBV during the first year post-transplantation. Herpes virus PCR tests for all included herpes viruses (CMV, EBV, HSV-1/2, and VZV) were retrieved from the Danish Microbiology database containing nationwide PCR results from both hospitals and outpatient clinics. Immune function was assessed by whole blood stimulation with A) LPS, B) R848, C) Poly I:C, and D) a blank control. Cytokine concentrations (TNF-α, IL-1β, IL-6, IL-8, IL-10, IL-12p40, IL-17A, IFN-α, and IFN-γ) were measured using Luminex. Results: We included 123 liver (54%), kidney (26%), and lung (20%) transplant recipients. The cumulative incidence of positive herpes virus PCR tests was 36.6% (95% CI: 28.1-45.1) during the first year post-transplantation. The final prediction model included recipient age, type of transplantation, CMV serostatus, and change in Poly I:C-induced IL-12p40 from pre-transplantation to three months post-transplantation. The prediction model had an AUC of 77% (95% CI: 61-92). Risk scores were extracted from the prediction model, and the participants were divided into three risk groups. Participants with a risk score <5 (28% of the cohort), 5-10 (45% of the cohort), and >10 (27% of the cohort) had a cumulative incidence of having a positive herpes virus PCR test at 5.8%, 25%, and 73%, respectively (p < 0.001). Conclusion: In conclusion, the incidence of positive herpes virus PCR tests was high, and a risk model including immune function allowed the prediction of positive herpes virus PCR and may be used to identify recipients at higher risk.

Indexed as

Cytomegalovirus InfectionsEpstein-Barr Virus InfectionsHerpesviridae InfectionsOrgan TransplantationCytomegalovirusHerpesvirus 2, HumanHerpesvirus 3, HumanHerpesvirus 4, HumanHumansImmunityInfantInterleukin-12 Subunit p40Poly IProspective StudiesInterleukin-12 Subunit p40Poly Icytomegalovirusherpes virusimmune functional assaypredictionsolid organ transplantationTruCulture®

Identifiers

PMID37465673
PMCPMC10351284
OpenAlexW4382940078

What Socratic 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 Socratic graph.