Evidence map›Paper›PMID 35363537›Full record

ReviewAnnual review of biomedical engineering2022

Improving Antibody Therapeutics by Manipulating the Fc Domain: Immunological and Structural Considerations.

George Delidakis, Jin Eyun Kim, Katia George, George Georgiou

Open access · hybridAbstract readReview
In one paragraph

Review in Annual review of biomedical engineering, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
9.4field-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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Association ofFrontiers in immunology · 2025
    Pooled it
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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

4 authors at 1 institution in 1 country.

George DelidakisDepartment of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA; email: gg@che.utexas.edu.
Jin Eyun KimDepartment of Biomedical Engineering, University of Texas at Austin, Austin, Texas, USA.
Katia GeorgeDepartment of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA.
George GeorgiouDepartment of Chemical Engineering, University of Texas at Austin, Austin, Texas, USA; email: gg@che.utexas.edu.
The University of Texas at Austin · US

Funding

Systematic, molecular level analysis of the Fc receptor ligation on antibody effector functionsU01AI148118 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI GEORGIOU, GEORGE GEORGIOU, VARADARAJAN, NAVIN · 2020 to 2024
$2.3M
NIAID NIH HHS U01 AI148118
6 · The paper itself

Abstract

Interactions between the crystallizable fragment (Fc) domain of antibodies and a plethora of cellular Fc receptors (FcRs) or soluble proteins form a critical link between humoral and innate immunity. In particular, the immunoglobulin G Fc domain is critical for the clearance of target cells by processes that include (

Indexed as

Immunoglobulin Fc FragmentsReceptors, FcAnimalsHumansImmunity, InnateMicePhagocytosisImmunoglobulin Fc FragmentsReceptors, FccytotoxicityFc engineeringFc receptorsmyeloid cellssignalingstructure

Identifiers

PMID35363537
PMCPMC9648538
OpenAlexW4220826711

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.