Evidence map›Paper›PMID 27559046›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

IgG Binding Characteristics of Rhesus Macaque FcγR.

Ying N Chan, Austin W Boesch, Nana Y Osei-Owusu, Ali Emileh, Andrew R Crowley, Sarah L Cocklin, Samantha L Finstad, Caitlyn H Linde, Rebecca A Howell, Isaac Zentner and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 48 citations in OpenAlex.

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  10. Complement contributes to antibody-mediated protection against repeated SHIV challenge.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

16 authors at 5 institutions in 1 country.

Ying N ChanThayer School of Engineering, Dartmouth College, Hanover, NH 03755;
Austin W BoeschThayer School of Engineering, Dartmouth College, Hanover, NH 03755;ORCID 0000-0003-2916-6744
Nana Y Osei-OwusuMolecular and Cellular Biology Program, Dartmouth College, Hanover, NH 03755;
Ali EmilehThayer School of Engineering, Dartmouth College, Hanover, NH 03755;
Andrew R CrowleyMolecular and Cellular Biology Program, Dartmouth College, Hanover, NH 03755;
Sarah L CocklinCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;ORCID 0000-0002-0165-7587
Samantha L FinstadCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;ORCID 0000-0002-3460-6428
Caitlyn H LindeCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;
Rebecca A HowellCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;ORCID 0000-0001-9136-0738
Isaac ZentnerDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102;ORCID 0000-0001-9828-271X
Simon CocklinDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102;ORCID 0000-0002-9074-741X
Adam R MilesWasatch Microfluidics, Salt Lake City, UT 84103; and.ORCID 0000-0002-1734-4171
Joshua W EckmanWasatch Microfluidics, Salt Lake City, UT 84103; and.ORCID 0000-0001-8981-8762
Galit AlterRagon Institute of MGH, MIT and Harvard, Cambridge, MA 02139.
Joern E SchmitzCenter for Virology and Vaccine Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115;ORCID 0000-0001-8803-0922
Margaret E AckermanThayer School of Engineering, Dartmouth College, Hanover, NH 03755; Molecular and Cellular Biology Program, Dartmouth College, Hanover, NH 03755; margaret.e.ackerman@dartmouth.edu.ORCID 0000-0002-4253-3476
Beth Israel Deaconess Medical Center · USDartmouth College · USCarterra (United States) · USDrexel University · USRagon Institute of MGH, MIT and Harvard · US

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI HAHN, BEATRICE H · 2012 to 2018
$204.7M
Physical Resources CoreP01AI120756 · NIAID · DUKE UNIVERSITY · PI TOMARAS, GEORGIA DORIS · 2016 to 2020
$17.1M
Applying High-Performance Protein Engineering Tools to HIV Immunogen DesignR01AI102691 · NIAID · DARTMOUTH COLLEGE · PI ACKERMAN, MARGARET E · 2012 to 2015
$2.2M
Role of Fc Receptor Polymorphisms in Antibody-Mediated ProtectionR56AI097315 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI SCHMITZ, JOERN E. · 2012 to 2012
$874k
NIAID NIH HHS HHSN272201100023CNIAID NIH HHS P01 AI120756NIAID NIH HHS R01 AI102691NIAID NIH HHS R56 AI097315NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

Indian rhesus macaques (Macaca mulatta) are routinely used in preclinical studies to evaluate therapeutic Abs and candidate vaccines. The efficacy of these interventions in many cases is known to rely heavily on the ability of Abs to interact with a set of Ab FcγR expressed on innate immune cells. Yet, despite their presumed functional importance, M. mulatta Ab receptors are largely uncharacterized, posing a fundamental limit to ensuring accurate interpretation and translation of results from studies in this model. In this article, we describe the binding characteristics of the most prevalent allotypic variants of M. mulatta FcγR for binding to both human and M. mulatta IgG of varying subclasses. The resulting determination of the affinity, specificity, and glycan sensitivity of these receptors promises to be useful in designing and evaluating studies of candidate vaccines and therapeutic Abs in this key animal model and exposes significant evolutionary divergence between humans and macaques.

Indexed as

AnimalsBinding SitesGenetic VariationHumansImmunoglobulin GMacaca mulattaReceptors, FcImmunoglobulin GReceptors, Fc

Identifiers

PMID27559046
PMCPMC5026948
OpenAlexW2513199205

What OpenQuestion holds

Textmetadata
LicenceTDM
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.