Evidence map›Paper›PMID 28566383›Full record

ArticleJournal of virology2017

Drug Modulators of B Cell Signaling Pathways and Epstein-Barr Virus Lytic Activation.

John G Kosowicz, Jaeyeun Lee, Brandon Peiffer, Zufeng Guo, Jianmeng Chen, Gangling Liao, S Diane Hayward, Jun O Liu, Richard F Ambinder

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  10. Mechanisms of organ transplant injury mediated by B cells and antibodies: Implications for antibody-mediated rejection.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2020
    Review
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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

9 authors at 2 institutions in 1 country.

John G KosowiczDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Jaeyeun LeeDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Brandon PeifferDepartment of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Zufeng GuoDepartment of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Jianmeng ChenDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Gangling LiaoDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
S Diane HaywardDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Jun O LiuDepartment of Pharmacology and Molecular Sciences, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Richard F AmbinderDepartment of Oncology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA rambind1@jhmi.edu.
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

Institute for Clinical and Translational ResearchUL1TR001079 · NCATS · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2013 to 2017
$60.1M
The Chemistry-Biology Interface Program at Johns Hopkins UniversityT32GM080189 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ROKITA, STEVEN E · 2008 to 2022
$3.5M
Herpesvirus protein kinases: Substrate recognition and pathway targeting.R21AI101377 · NIAID · JOHNS HOPKINS UNIVERSITY · PI HAYWARD, S DIANE · 2012 to 2013
$433k
Plasma and serum biomarkers for Hodgkin lymphomaR21CA188824 · NCI · JOHNS HOPKINS UNIVERSITY · PI AMBINDER, RICHARD FREDERICK · 2014 to 2015
$420k
NCATS NIH HHS UL1 TR001079NCI NIH HHS R21 CA188824NIAID NIH HHS R21 AI101377NIGMS NIH HHS T32 GM080189
6 · The paper itself

Abstract

Epstein-Barr virus (EBV) is a ubiquitous human gammaherpesvirus that establishes a latency reservoir in B cells. In this work, we show that ibrutinib, idelalisib, and dasatinib, drugs that block B cell receptor (BCR) signaling and are used in the treatment of hematologic malignancies, block BCR-mediated lytic induction at clinically relevant doses. We confirm that the immunosuppressive drugs cyclosporine and tacrolimus also inhibit BCR-mediated lytic induction but find that rapamycin does not inhibit BCR-mediated lytic induction. Further investigation shows that mammalian target of rapamycin complex 2 (mTORC2) contributes to BCR-mediated lytic induction and that FK506-binding protein 12 (FKBP12) binding alone is not adequate to block activation. Finally, we show that BCR signaling can activate EBV lytic induction in freshly isolated B cells from peripheral blood mononuclear cells (PBMCs) and that activation can be inhibited by ibrutinib or idelalisib.

Indexed as

B-LymphocytesHerpesvirus 4, HumanHumansImmunologic FactorsReceptors, Antigen, B-CellSignal TransductionVirus ActivationImmunologic FactorsReceptors, Antigen, B-CellB cell receptor pathwaycyclosporinedasatinibEpstein-Barr virusibrutinibidelalisiblytic infectionmTORrapamycintacrolimus

Identifiers

PMID28566383
PMCPMC5533897
OpenAlexW2617832733

What OpenQuestion 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 OpenQuestion graph.