Evidence map›Paper›PMID 42589383›Full record

ReviewInternational journal of molecular sciences2026

Mechanisms and Determinants of CMV Reactivation in Kidney Transplantation.

Ruchi Naik, Walaa Dabbas, Benito Veldepenas, Demetrius Harvell, Fares Eshac, Megan Trivedi, Carlo Minicucci, Mary Hummel, Zheng Jenny Zhang, Lorenzo Gallon and 1 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Ruchi NaikDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Walaa DabbasDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.ORCID 0009-0007-2033-279X
Benito VeldepenasDivision of Transplantation, Department of Surgery, University of Illinois Chicago, Chicago, IL 60612, USA.
Demetrius HarvellDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Fares EshacDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Megan TrivediDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Carlo MinicucciDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Mary HummelDepartment of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0001-6277-4405
Zheng Jenny ZhangDepartment of Surgery, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0001-6469-5778
Lorenzo GallonDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.
Eleonora ForteDivision of Nephrology, Department of Medicine, University of Illinois College of Medicine, Chicago, IL 60612, USA.ORCID 0000-0002-6095-2797

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human cytomegalovirus (CMV) remains a significant infectious complication after kidney transplantation, reflecting gaps in the understanding of the molecular and immunological mechanisms regulating the transition from latency to productive infection. Following primary infection, CMV establishes lifelong latency in hematopoietic and myeloid lineage cells, maintained by viral chromatin repression and robust CMV-specific immune surveillance. CMV reactivation is associated with graft dysfunction, increased risk of rejection, opportunistic infections, and reduced patient survival. In kidney transplantation, CMV reactivation is driven by the interplay between tissue injury, inflammation, and immunosuppression. Ischemia-reperfusion injury and peri-operative stress produce reactive oxygen species, DNA damage, and pro-inflammatory cytokines (e.g., TNF-α, IL-6), which activate transcription factors such as NF-κB and AP-1. These factors regulate the CMV major immediate-early promoter (MIEP), thereby triggering lytic viral gene expression. At the same time, immunosuppressive therapies impair antiviral immune surveillance and, in some cases, induce cytokine release, potentially contributing to the pro-inflammatory environment that favors viral reactivation. In this review, we summarize current molecular and immunologic mechanisms governing CMV latency and reactivation with a focus on how immunosuppressive strategies and injury-associated pathways converge to promote CMV reactivation. We also discuss implications of risk stratification and the development of targeted therapeutic strategies to prevent CMV reactivation in kidney transplant recipients (KTRs).

Indexed as

CytomegalovirusCytomegalovirus InfectionsKidney TransplantationVirus ActivationHumansImmunosuppressive AgentsVirus LatencyImmunosuppressive AgentsCMVepigeneticsimmunosuppressioninflammationkidney transplantreactivation

Identifiers

PMID42589383
PMCPMC13466323

What Socratic 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 Socratic graph.