"Receptors, IgG" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Specific molecular sites on the surface of various cells, including B-lymphocytes and macrophages, that combine with IMMUNOGLOBULIN Gs. Three subclasses exist: Fc gamma RI (the CD64 antigen, a low affinity receptor), Fc gamma RII (the CD32 antigen, a high affinity receptor), and Fc gamma RIII (the CD16 antigen, a low affinity receptor).
| Descriptor ID |
D017452
|
| MeSH Number(s) |
D12.776.543.750.705.871.300
|
| Concept/Terms |
Receptors, IgG- Receptors, IgG
- IgG Receptors
- gamma Fc Receptors
- Fc gamma Receptors
- gamma Receptors, Fc
- Receptors, Fc gamma
- Immunoglobulin G Receptor
- Receptor, Immunoglobulin G
- Fc Receptors, gamma
- Receptors, gamma Fc
CD32 Antigens- CD32 Antigens
- CD 32 Antigens
- Antigens, CD 32
- Fc gamma RII
- gamma RII, Fc
- Antigens, CD32
CD64 Antigens- CD64 Antigens
- CD 64 Antigens
- Antigens, CD 64
- Fc gamma RI
- gamma RI, Fc
- Antigens, CD64
Antigens, CD16- Antigens, CD16
- Fc gamma RIII
- gamma RIII, Fc
- CD 16 Antigens
- Antigens, CD 16
- CD16 Antigens
|
Below are MeSH descriptors whose meaning is more general than "Receptors, IgG".
Below are MeSH descriptors whose meaning is more specific than "Receptors, IgG".
This graph shows the total number of publications written about "Receptors, IgG" by people in this website by year, and whether "Receptors, IgG" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 1 | 0 | 1 |
| 2012 | 0 | 2 | 2 |
| 2013 | 1 | 0 | 1 |
| 2015 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 1 | 2 |
| 2019 | 1 | 0 | 1 |
| 2021 | 2 | 1 | 3 |
| 2022 | 1 | 1 | 2 |
| 2024 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Receptors, IgG" by people in Profiles.
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SARS-CoV-2 BA.4/5 infection triggers more cross-reactive Fc?RIIIa signaling and neutralization than BA.1, in the context of hybrid immunity. J Virol. 2024 Jul 23; 98(7):e0067824.
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FCGR3A gene duplication, Fc?RIIb-232TT and Fc?RIIIb-HNA1a associate with an increased risk of vertical acquisition of HIV-1. PLoS One. 2022; 17(9):e0273933.
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Functional consequences of allotypic polymorphisms in human immunoglobulin G subclasses. Immunogenetics. 2023 02; 75(1):1-16.
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Fc?R Genetic Variation and HIV-1 Vaccine Efficacy: Context And Considerations. Front Immunol. 2021; 12:788203.
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An HIV Vaccine Protective Allele in FCGR2C Associates With Increased Odds of Perinatal HIV Acquisition. Front Immunol. 2021; 12:760571.
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HIV Broadly Neutralizing Antibodies Expressed as IgG3 Preserve Neutralization Potency and Show Improved Fc Effector Function. Front Immunol. 2021; 12:733958.
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Chronic HIV-1 Infection Alters the Cellular Distribution of Fc?RIIIa and the Functional Consequence of the Fc?RIIIa-F158V Variant. Front Immunol. 2019; 10:735.
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The FCGR2C allele that modulated the risk of HIV-1 infection in the Thai RV144 vaccine trial is implicated in HIV-1 disease progression. Genes Immun. 2019 11; 20(8):651-659.
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Measuring the ability of HIV-specific antibodies to mediate trogocytosis. J Immunol Methods. 2018 12; 463:71-83.
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Perinatal HIV-1 transmission: Fc gamma receptor variability associates with maternal infectiousness and infant susceptibility. Retrovirology. 2016 06 10; 13(1):40.