Evidence map›Paper›PMID 25045879›Full record

ReviewNature immunology2014

Type I and type II Fc receptors regulate innate and adaptive immunity.

Andrew Pincetic, Stylianos Bournazos, David J DiLillo, Jad Maamary, Taia T Wang, Rony Dahan, Benjamin-Maximillian Fiebiger, Jeffrey V Ravetch

Open access · greenAbstract readReview
In one paragraph

Review in Nature immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 294 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
294citing papers in PubMed, 1 pooled it
37.3field-weighted citation impact, top 1% 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

294 citing papers in PubMed, 1 synthesis or guideline pooled it, 494 citations in OpenAlex.

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234 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

8 authors at 1 institution in 1 country.

Andrew Pincetic1] The Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA. [2].
Stylianos Bournazos1] The Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA. [2].
David J DiLillo1] The Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA. [2].
Jad MaamaryThe Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA.
Taia T WangThe Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA.
Rony DahanThe Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA.
Benjamin-Maximillian FiebigerThe Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA.
Jeffrey V RavetchThe Laboratory of Molecular Genetics and Immunology, The Rockefeller University, New York, New York, USA.
Rockefeller University · US

Funding

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
NIAID NIH HHS U19 AI109946
6 · The paper itself

Abstract

Antibodies produced in response to a foreign antigen are characterized by polyclonality, not only in the diverse epitopes to which their variable domains bind but also in the various effector molecules to which their constant regions (Fc domains) engage. Thus, the antibody's Fc domain mediates diverse effector activities by engaging two distinct classes of Fc receptors (type I and type II) on the basis of the two dominant conformational states that the Fc domain may adopt. These conformational states are regulated by the differences among antibody subclasses in their amino acid sequence and by the complex, biantennary Fc-associated N-linked glycan. Here we discuss the diverse downstream proinflammatory, anti-inflammatory and immunomodulatory consequences of the engagement of type I and type II Fc receptors in the context of infectious, autoimmune, and neoplastic disorders.

Indexed as

Adaptive ImmunityImmunity, InnateAmino Acid SequenceAntibodiesAntigen PresentationAutoimmune DiseasesGlycosylationHumansImmunoglobulin Fc FragmentsImmunoglobulin GNeoplasmsProtein ConformationProtein Structure, TertiaryReceptors, IgGVaccinationAntibodiesImmunoglobulin Fc FragmentsImmunoglobulin GReceptors, IgG

Identifiers

PMID25045879
PMCPMC7430760
OpenAlexW2116661011

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.