Evidence map›Paper›PMID 34502398›Full record

ReviewInternational journal of molecular sciences2021

Fc Receptor Variants and Disease: A Crucial Factor to Consider in the Antibody Therapeutics in Clinic.

Jin Kim, Ji Young Lee, Han Gil Kim, Min Woo Kwak, Tae Hyun Kang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Evaluation ofFrontiers in medicine · 2026
    Pooled it
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  3. Article
  4. Review
  5. Review
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  11. Rhesus Macaques: VNTR Polymorphism of the FCGRT Gene.Bulletin of experimental biology and medicine · 2024
    Article
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  13. Article
  14. Review
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.

Jin KimDepartment of Interdisciplinary Program for Bio-Health Convergence, Kookmin University, Seoul 02707, Korea.
Ji Young LeeDepartment of Chemistry, Kookmin University, Seoul 02707, Korea.
Han Gil KimDepartment of Biopharmaceutical Chemistry, Kookmin University, Seoul 02707, Korea.
Min Woo KwakDepartment of Biopharmaceutical Chemistry, Kookmin University, Seoul 02707, Korea.
Tae Hyun KangDepartment of Interdisciplinary Program for Bio-Health Convergence, Kookmin University, Seoul 02707, Korea.ORCID 0000-0002-7825-5877
Kookmin University · KR

Funding

the Korean government NRF-2020R1F1A1072124
6 · The paper itself

Abstract

The fragment crystallizable (Fc) domain of antibodies is responsible for their protective function and long-lasting serum half-life via Fc-mediated effector function, transcytosis, and recycling through its interaction with Fc receptors (FcRs) expressed on various immune leukocytes, epithelial, and endothelial cells. Therefore, the Fc-FcRs interaction is a control point of both endogenous and therapeutic antibody function. There are a number of reported genetic variants of FcRs, which include polymorphisms in (i) extracellular domain of FcRs, which change their affinities to Fc domain of antibodies; (ii) both cytoplasmic and intracellular domain, which alters the extent of signal transduction; and (iii) the promoter region of the FcRs gene, which affects the expression level of FcRs, thus being associated with the pathogenesis of disease indications. In this review, we firstly describe the correlation between the genetic variants of FcRs and immunological disorders by individual differences in the extent of FcRs-mediated regulations. Secondly, we discuss the influence of the genetic variants of FcRs on the susceptibility to infectious diseases or cancer in the perspective of FcRs-induced effector functions. Overall, we concluded that the genetic variants of FcRs are one of the key elements in the design of antibody therapeutics due to their variety of clinical outcomes among individuals.

Indexed as

AnimalsAntibodiesAutoimmune DiseasesCommunicable DiseasesGenetic VariationHumansImmunoglobulin Fc FragmentsImmunotherapyNeoplasmsReceptors, FcAntibodiesImmunoglobulin Fc FragmentsReceptors, Fcantibody engineeringcancerFcRsgenetic variantsimmunological disordersinfectious diseases

Identifiers

PMID34502398
PMCPMC8431278
OpenAlexW3197398982

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.