Evidence map›Paper›PMID 21460204›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2011

EBV-specific CD8+ T cells from asymptomatic pediatric thoracic transplant patients carrying chronic high EBV loads display contrasting features: activated phenotype and exhausted function.

Camila Macedo, Steven A Webber, Albert D Donnenberg, Iulia Popescu, Yun Hua, Michael Green, David Rowe, Louise Smith, Maria M Brooks, Diana Metes

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
–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

28 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  10. Review
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  13. Article
  14. Virus-specific T cells in pediatric renal transplantation.Pediatric nephrology (Berlin, Germany) · 2021
    Review
  15. Biomarkers for PTLD diagnosis and therapies.Pediatric nephrology (Berlin, Germany) · 2020
    Review
  16. Article
  17. LPAFrontiers in immunology · 2019
    Article
  18. Article
  19. Article
  20. 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

10 authors.

Camila MacedoThomas E. Starzl Transplantation Institute, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
Steven A Webber
Albert D Donnenberg
Iulia Popescu
Yun Hua
Michael Green
David Rowe
Louise Smith
Maria M Brooks
Diana Metes

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Leonard J. Appleman · 1988 to 2026
$158.0M
Transplant EBV Disease: Pathogenesis and ImmunotherapyP50HL074732 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KELLER, BRADLEY BARTH · 2004 to 2008
$12.2M
NCI NIH HHS P30 CA047904NHLBI NIH HHS 5 P50 HL074732-03NHLBI NIH HHS P50 HL074732
6 · The paper itself

Abstract

Serial EBV load monitoring of clinically asymptomatic pediatric thoracic organ transplant patients has identified three groups of children who exhibit undetectable (<100 copies/ml), chronic low (100-16,000 copies/ml), or chronic high (>16,000 copies/ml) EBV loads in peripheral blood. Chronic high EBV load patients have a 45% rate of progression to late-onset posttransplant lymphoproliferative disorders. In this article, we report that asymptomatic patients carrying EBV loads (low and high) expressed increased frequencies of EBV-specific CD8(+) T cells, as compared with patients with undetectable EBV loads. Although patients with low viral load displayed EBV-specific CD8(+) T cells with moderate signs of activation (CD38(+/-)/CD127(+/-)), programmed death 1 upregulation and effective IFN-γ secretion, high EBV load carriers showed significant CD38(+) upregulation, features of cellular exhaustion (programmed death 1(+)/CD127(-)) accompanied by a decline in IFN-γ release. Immunopolarization of EBV-specific CD8(+) T cells was skewed from the expected type 1 (IFN-γ) toward type 0 (IFN-γ/IL-5) in patients, and Tr1 (IL-10) in high load carriers. These results indicate the importance of chronic EBV load and of the levels of antigenic pressure in shaping EBV-specific memory CD8(+) T cells. Concomitant phenotypic and functional EBV monitoring is critical for identifying the complex "functional" versus "exhausted" signature of EBV-specific CD8(+) T cells, with implications for immunologic monitoring in the clinic.

Indexed as

AdolescentADP-ribosyl Cyclase 1ApoptosisAsymptomatic InfectionsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesChildChild, PreschoolEpstein-Barr Virus InfectionsFemaleFlow CytometryHeart TransplantationHerpesvirus 4, HumanHumansImmunologic MemoryInterferon-gammaADP-ribosyl Cyclase 1Interferon-gammaInterleukin-10Interleukin-5Interleukin-7 Receptor alpha Subunit

Identifiers

PMID21460204
PMCPMC4165085

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.