Evidence map›Paper›PMID 28033393›Full record

ArticlePloS one2016

Regulatory T Cells in Endemic Burkitt Lymphoma Patients Are Associated with Poor Outcomes: A Prospective, Longitudinal Study.

Emily Parsons, Juliana A Otieno, John Michael Ong'echa, Christina E Nixon, John Vulule, Christian Münz, V Ann Stewart, Ann M Moormann

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  8. A New Hope for CD56Frontiers in cellular and infection microbiology · 2020
    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

8 authors at 6 institutions in 3 countries.

Emily ParsonsUniformed Services University of the Health Sciences, Bethesda, MD United States of America.
Juliana A OtienoJaramogi Oginga Odinga Teaching and Referral Hospital, Ministry of Health, Kisumu, Kenya.
John Michael Ong'echaCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Christina E NixonCenter for International Health and the Department of Pathology, Rhode Island Hospital, Providence, RI United States of America.
John VululeCenter for Global Health Research, Kenya Medical Research Institute, Kisumu, Kenya.
Christian MünzDepartment of Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, Zürich, Switzerland.
V Ann StewartUniformed Services University of the Health Sciences, Bethesda, MD United States of America.
Ann M MoormannProgram in Molecular Medicine, University of Massachusetts Medical School, Worcester, MA United States of America.
Kenya Medical Research Institute · KEUniformed Services University of the Health Sciences · USMinistry of Health · KERhode Island Hospital · USUniversity of Massachusetts Chan Medical School · USUniversity of Zurich · CH

Funding

Impact of malaria on shaping immunity to EBV in the etiology of Burkitt lymphomaR01CA189806 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MOORMANN, ANN M · 2014 to 2024
$5.7M
T Cell Immunity in Endemic Burkitt LymphomaR01CA134051 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MOORMANN, ANN M · 2008 to 2012
$2.3M
NCI NIH HHS R01 CA134051NCI NIH HHS R01 CA189806Worldwide Cancer Research 14-1033
6 · The paper itself

Abstract

Deficiencies in Epstein-Barr virus (EBV)-specific T cell immunosurveillance appear to precede the development of endemic Burkitt lymphoma (eBL), a malaria-associated pediatric cancer common in sub-Saharan Africa. However, T cell contributions to eBL disease progression and survival have not been characterized. Our objective was to investigate regulatory and inflammatory T cell responses in eBL patients associated with clinical outcomes. By multi-parameter flow cytometry, we examined peripheral blood mononuclear cells from 38 eBL patients enrolled in a prospective cohort study in Kisumu, Kenya from 2008-2010, and 14 healthy age-matched Kenyan controls. Children diagnosed with eBL were prospectively followed and outcomes categorized as 2-year event-free survivors, cases of relapses, or those who died. At the time of diagnosis, eBL children with higher CD25+Foxp3+ regulatory T (Treg) cell frequencies were less likely to survive than patients with lower Treg frequencies (p = 0·0194). Non-survivors also had higher absolute counts of CD45RA+Foxp3lo naïve and CD45RA-Foxp3hi effector Treg subsets compared to survivors and healthy controls. Once patients went into clinical remission, Treg frequencies remained low in event-free survivors. Patients who relapsed, however, showed elevated Treg frequencies months prior to their adverse event. Neither concurrent peripheral blood EBV load nor malaria infection could explain higher Treg cell frequencies. CD8+ T cell PD-1 expression was elevated in all eBL patients at time of diagnosis, but relapse patients tended to have persistently high PD-1 expression compared to long-term survivors. Non-survivors produced more CD4+ T-cell IL-10 in response to both Epstein-Barr Nuclear Antigen-1 (EBNA-1) (p = 0·026) and the malaria antigen Plasmodium falciparum Schizont Egress Antigen-1 (p = 0·0158) compared to survivors, and were concurrently deficient in (EBNA-1)-specific CD8+ T-cell derived IFN-γ production (p = 0·002). In addition, we identified the presence of Foxp3-IL10+ regulatory Type 1 cells responding to EBNA-1 in contrast to the malaria antigen tested. These novel findings suggest that poor outcomes in eBL patients are associated with a predominantly immuno-regulatory environment. Therefore, Treg frequencies could be a predictive biomarker of disease progression and manipulation of Treg activity has potential as a therapeutic target to improve eBL survival.

Indexed as

AdolescentAntigens, ProtozoanBiomarkersBurkitt LymphomaCD4 Lymphocyte CountCD8-Positive T-LymphocytesCells, CulturedChildChild, PreschoolEpstein-Barr Virus Nuclear AntigensHerpesvirus 4, HumanHumansImmunologic SurveillanceInterleukin-10KenyaLongitudinal StudiesAntigens, ProtozoanBiomarkersEBV-encoded nuclear antigen 1Epstein-Barr Virus Nuclear AntigensIL10 protein, humanInterleukin-10PDCD1 protein, humanProgrammed Cell Death 1 ReceptorProtozoan ProteinsSEA-1 protein, Plasmodium falciparum

Identifiers

PMID28033393
PMCPMC5199096
OpenAlexW2565135645

What OpenQuestion holds

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LicenceCC0
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 OpenQuestion graph.