Evidence map›Paper›PMID 27825564›Full record

ArticleCellular immunology2017

Genetic markers of immunoglobulin G and immunity to cytomegalovirus in patients with breast cancer.

Janardan P Pandey, Aryan M Namboodiri, Sarumathi Mohan, Paul J Nietert, Lindsay Peterson

Open access · greenAbstract read
In one paragraph

Article in Cellular immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Breast cancer and cytomegalovirus.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 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

5 authors at 1 institution in 1 country.

Janardan P PandeyDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, USA. Electronic address: pandeyj@musc.edu.
Aryan M NamboodiriDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, USA.
Sarumathi MohanDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC 29425, USA.
Paul J NietertDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
Lindsay PetersonDepartment of Medicine, Medical University of South Carolina, Charleston, SC 29425, USA.
Medical University of South Carolina · US

Funding

Subproject Title: Clinical Research Education, Mentoring and Career Development CoreU54GM104941 · NIGMS · UNIVERSITY OF DELAWARE · PI LEE M PACHTER · 2013 to 2026
$60.5M
Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
Patient Resource CoreP60AR062755 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GILKESON, GARY S · 2012 to 2016
$5.8M
NCATS NIH HHS UL1 TR001450NCI NIH HHS P30 CA138313NIAMS NIH HHS P60 AR062755NIGMS NIH HHS U54 GM104941
6 · The paper itself

Abstract

Human cytomegalovirus (CMV), a ubiquitous herpesvirus, has been implicated in the etiology of breast cancer. It is clear that not all people exposed to CMV are equally likely to develop this malignancy, implying the presence of host genetic factors that might modulate the cancer-spurring properties of the virus. CMV has evolved sophisticated strategies for evading host immunosurveillance. One strategy involves encoding decoy Fcγ receptors (FcγR) that thwart the Fcγ-mediated effector functions, such as antibody-dependent cellular cytotoxicity. In this investigation, using an enzyme-linked immunosorbent assay (ELISA), we aimed to determine whether the decoy FcγR encoded by the CMV gene RL13 binds differentially to anti-CMV antibodies expressing different immunoglobulin GM (γ marker) allotypes, genetic markers of immunoglobulin G (IgG). Results of our ELISA binding studies showed that the absorbance values for the binding of the viral FcγR to the GM 17-expressing IgG antibodies were significantly higher than for the GM 3-expressing antibodies (0.60 vs. 0.36; p=0.0019). These findings provide mechanistic insights into the modulating role played by the genetic variants of IgG in the generation of immunity to CMV in patients with breast cancer.

Indexed as

AdultAgedAntibodies, ViralAntibody AffinityBlack or African AmericanBreast NeoplasmsCytomegalovirusCytomegalovirus InfectionsFemaleGenetic Predisposition to DiseaseGenotypeHumansImmune EvasionImmunoglobulin GImmunoglobulin Gm AllotypesMiddle AgedAntibodies, ViralImmunoglobulin GImmunoglobulin Gm AllotypesReceptors, IgGViral ProteinsCytomegalovirusDecoy Fcγ receptorGM allotypesImmunoevasion

Identifiers

PMID27825564
PMCPMC5290197
OpenAlexW2547484557

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.