Evidence map›Paper›PMID 28446061›Full record

ReviewAnnual review of immunology2017

Signaling by Antibodies: Recent Progress.

Stylianos Bournazos, Taia T Wang, Rony Dahan, Jad Maamary, Jeffrey V Ravetch

Abstract readReview
In one paragraph

Review in Annual review of immunology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 163 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed, 3 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

163 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Review
  7. Four IgG Antibodies and Protein G Are Shapeshifters.International journal of molecular sciences · 2026
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  13. Recurrent mutations drive rapid HIV escape from two broadly neutralizing antibodies in vivo.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  14. Review
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103 more citing papers are in PubMed but not listed here.

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.

Stylianos BournazosLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York 10065; email: ravetch@rockefeller.edu.
Taia T WangLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York 10065; email: ravetch@rockefeller.edu.
Rony DahanLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York 10065; email: ravetch@rockefeller.edu.
Jad MaamaryLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York 10065; email: ravetch@rockefeller.edu.
Jeffrey V RavetchLaboratory of Molecular Genetics and Immunology, The Rockefeller University, New York 10065; email: ravetch@rockefeller.edu.

Funding

Stuctural basis of bNab activityP01AI100148 · NIAID · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI Pamela J Bjorkman · 2013 to 2026
$43.3M
Transforming Translational Science and Education to Benefit Human HealthUL1TR000043 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2012 to 2015
$26.8M
Understanding B cell memory in response to diverse virus infectionsU19AI111825 · NIAID · ROCKEFELLER UNIVERSITY · PI RAVETCH, JEFFREY VICTOR · 2014 to 2023
$26.0M
Molecular mechanisms of antibody-mediated immunotherapiesR35CA196620 · NCI · ROCKEFELLER UNIVERSITY · PI JEFFREY Victor RAVETCH · 2016 to 2026
$11.5M
Personalized Immunotherapy of Patients with Ovarian CancerP01CA190174 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI SABBATINI, PAUL J, SPRIGGS, DAVID R · 2015 to 2019
$10.5M
Understanding Human B Cell Responses to Influenza to Improve the Influenza U19AI109946 · NIAID · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI RAVETCH, JEFFREY VICTOR · 2014 to 2018
$9.6M
NCATS NIH HHS UL1 TR000043NCI NIH HHS P01 CA190174NCI NIH HHS R35 CA196620NIAID NIH HHS P01 AI100148NIAID NIH HHS U19 AI109946NIAID NIH HHS U19 AI111825
6 · The paper itself

Abstract

IgG antibodies mediate a diversity of immune functions by coupling of antigen specificity through the Fab domain to signal transduction via Fc-Fc receptor interactions. Indeed, balanced IgG signaling through type I and type II Fc receptors is required for the control of proinflammatory, anti-inflammatory, and immunomodulatory processes. In this review, we discuss the mechanisms that govern IgG-Fc receptor interactions, highlighting the diversity of Fc receptor-mediated effector functions that regulate immunity and inflammation as well as determine susceptibility to infection and autoimmunity and responsiveness to antibody-based therapeutics and vaccines.

Indexed as

AnimalsAntibodiesAutoimmune DiseasesDisease SusceptibilityHumansImmunity, HumoralImmunoglobulin GImmunotherapyInfectionsInflammationReceptors, FcSignal TransductionAntibodiesImmunoglobulin GReceptors, Fceffector functionFc receptorsIgGimmunityimmunomodulationinflammation

Identifiers

PMID28446061
PMCPMC5613280

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.