Evidence map›Paper›PMID 33704812›Full record

ArticleJournal of medical virology2021

Evidence of Epstein-Barr virus heterogeneous gene expression in adult lung transplant recipients with posttransplant lymphoproliferative disorder.

Lorenzo Zaffiri, Courtney Frankel, Erika J Bush, Megan L Neely, Elizabeth N Pavlisko, Irina L Mokrova, Micah A Luftig, Scott M Palmer

Open access · greenAbstract read
In one paragraph

Article in Journal of medical virology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

8 authors at 1 institution in 1 country.

Lorenzo ZaffiriDepartment of Medicine, Duke University, Durham, North Carolina, USA.ORCID 0000-0002-8369-4145
Courtney FrankelDepartment of Medicine, Duke University, Durham, North Carolina, USA.
Erika J BushDepartment of Medicine, Duke University, Durham, North Carolina, USA.
Megan L NeelyDepartment of Biostatistics and Bioinformatics, Duke University, Durham, North Carolina, USA.
Elizabeth N PavliskoDepartment of Pathology, Duke University, Durham, North Carolina, USA.
Irina L MokrovaDepartment of Medicine, Duke University, Durham, North Carolina, USA.
Micah A LuftigDepartment of Molecular Genetics and Microbiology, Duke Center for Virology, Duke University, Durham, North Carolina, USA.
Scott M PalmerDepartment of Medicine, Duke University, Durham, North Carolina, USA.
Duke University · US

Funding

Noninvasive Markers and Transplant Outcome in HumansU01AI063594 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HEEGER, PETER SCOTT · 2004 to 2022
$66.5M
Host pathways regulating Epstein-Barr virus-mediated B cell growth transformationR01CA140337 · NCI · DUKE UNIVERSITY · PI LUFTIG, MICAH ALAN · 2011 to 2025
$5.9M
Targeting Apoptosis and Immune Control of Epstein-Barr Virus Infected Tonsillar B CellsR01DE025994 · NIDCR · DUKE UNIVERSITY · PI Micah Alan Luftig · 2016 to 2026
$5.0M
NCI NIH HHS R01 CA140337NIAID NIH HHS U01 AI063594NIDCR NIH HHS R01 DE025994
6 · The paper itself

Abstract

Epstein-Barr virus (EBV)-driven posttransplant lymphoproliferative disorder (PTLD) is a serious complication following lung transplant. The extent to which the presence of EBV in PTLD tissue is associated with survival is uncertain. Moreover, whether the heterogeneity in expression of EBV latency programs is related to the timing of PTLD onset remains unexplored. We retrospectively performed a comprehensive histological evaluation of EBV markers at the tissue level in 34 adult lung transplant recipients with early- and late-onset PTLD. Early-onset PTLD, occurring within the first 12 months posttransplant, had higher odds to express EBV markers. The presence of EBV in PTLD was not associated with a difference in survival relative to EBV-negative tumors. However, we found evidence of heterogeneous expression of EBV latency programs, including type III, IIb, IIa, and 0/I. Our study suggests that the heterogeneous expression of EBV latency programs may represent a mechanism for immune evasion in patients with PLTD after lung transplants. The recognition of multiple EBV latency programs can be used in personalized medicine in patients who are nonresponsive to traditional types of chemotherapy and can be potentially evaluated in other types of solid organ transplants.

Indexed as

AdultEpstein-Barr Virus InfectionsFemaleGene ExpressionHerpesvirus 4, HumanHumansLungLymphoproliferative DisordersMaleMiddle AgedOrgan TransplantationRetrospective StudiesTransplant RecipientsViral ProteinsVirus LatencyViral ProteinsEBV latency programEpstein-Barr viruslung transplantPTLDPTLD survival

Identifiers

PMID33704812
PMCPMC9208898
OpenAlexW3135247783

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.