Evidence map›Paper›PMID 28376031›Full record

ReviewTransplantation2017

The Immune Response to Epstein Barr Virus and Implications for Posttransplant Lymphoproliferative Disorder.

Olivia M Martinez, Sheri M Krams

Open access · greenAbstract readReview
In one paragraph

Review in Transplantation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

42 citing papers in PubMed, 90 citations in OpenAlex.

  1. Review
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  19. Mutations in latent membrane protein 1 of Epstein-Barr virus are associated with increased risk of posttransplant lymphoproliferative disorder in children.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    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

2 authors at 1 institution in 1 country.

Olivia M Martinez1 Division of Abdominal Transplantation and Program in Immunology, Department of Surgery, Stanford University School of Medicine, Stanford, CA.
Sheri M Krams
Stanford Medicine · US

Funding

Biomarkers for Post-Transplant Lymphoproliferative Disorders in ChildrenU01AI104342 · NIAID · STANFORD UNIVERSITY · PI ESQUIVEL, CARLOS O · 2013 to 2018
$7.7M
New Therapeutics for Post-Transplant Lymphoproliferative DisorderR01AI113130 · NIAID · STANFORD UNIVERSITY · PI MARTINEZ, OLIVIA M · 2016 to 2020
$2.0M
Plasmacytoid Dendritic Cell microRNAS in TransplantationR21AI119686 · NIAID · STANFORD UNIVERSITY · PI KRAMS, SHERI M. · 2016 to 2017
$440k
Targeting B Cell MicroRNA in Post-Transplant EBV-Associated B Cell LymphomaR21AI115313 · NIAID · STANFORD UNIVERSITY · PI MARTINEZ, OLIVIA M · 2016 to 2017
$435k
NIAID NIH HHS R01 AI113130NIAID NIH HHS R21 AI115313NIAID NIH HHS R21 AI119686NIAID NIH HHS U01 AI104342
6 · The paper itself

Abstract

Posttransplant lymphoproliferative disorder (PTLD) is a serious complication in organ transplant recipients and is most often associated with the Epstein Barr virus (EBV). EBV is a common gammaherpes virus with tropism for B lymphocytes and infection in immunocompetent individuals is typically asymptomatic and benign. However, infection in immunocompromised or immunosuppressed individuals can result in malignant B cell lymphoproliferations, such as PTLD. EBV+ PTLD can arise after primary EBV infection, or because of reactivation of a prior infection, and represents a leading malignancy in the transplant population. The incidence of EBV+ PTLD is variable depending on the organ transplanted and whether the recipient has preexisting immunity to EBV but can be as high as 20%. It is generally accepted that impaired immune function due to immunosuppression is a primary cause of EBV+ PTLD. In this overview, we review the EBV life cycle and discuss our current understanding of the immune response to EBV in healthy, immunocompetent individuals, in transplant recipients, and in PTLD patients. We review the strategies that EBV uses to subvert and evade host immunity and discuss the implications for the development of EBV+ PTLD.

Indexed as

AnimalsEpstein-Barr Virus InfectionsHerpesvirus 4, HumanHost-Pathogen InteractionsHumansImmunity, HumoralImmunocompromised HostImmunosuppressive AgentsKiller Cells, NaturalLymphoproliferative DisordersOpportunistic InfectionsOrgan TransplantationRisk AssessmentRisk FactorsT-LymphocytesTreatment OutcomeImmunosuppressive Agents

Identifiers

PMID28376031
PMCPMC5568952
OpenAlexW2604929726

What OpenQuestion holds

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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.