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<scp>TRIM</scp> 21: a cytosolic Fc receptor with broad antibody isotype specificity
- Source :
- Immunological Reviews
- Publication Year :
- 2015
- Publisher :
- Wiley, 2015.
-
Abstract
- Antibodies are key molecules in the fight against infections. Although previously thought to mediate protection solely in the extracellular environment, recent research has revealed that antibody-mediated protection extends to the cytosolic compartment of cells. This postentry viral defense mechanism requires binding of the antibody to a cytosolic Fc receptor named tripartite motif containing 21 (TRIM21). In contrast to other Fc receptors, TRIM21 shows remarkably broad isotype specificity as it does not only bind IgG but also IgM and IgA. When viral pathogens coated with these antibody isotypes enter the cytosol, TRIM21 is rapidly recruited and efficient neutralization occurs before the virus has had the time to replicate. In addition, inflammatory signaling is induced. As such, TRIM21 acts as a cytosolic sensor that engages antibodies that have failed to protect against infection in the extracellular environment. Here, we summarize our current understanding of how TRIM21 orchestrates humoral immunity in the cytosolic environment.
- Subjects :
- Models, Molecular
Protein Conformation
Ubiquitin-Protein Ligases
isotype
Immunology
Fc receptor
virus
Immunoglobulin G
03 medical and health sciences
Cytosol
0302 clinical medicine
Antibody Isotype
Antibody Specificity
Animals
Humans
antibodies
Immunology and Allergy
Protein Interaction Domains and Motifs
Invited Reviews
Receptor
030304 developmental biology
0303 health sciences
biology
intracellular immunity
Immunoglobulin Fc Fragments
Immunity
Antibodies, Neutralizing
Isotype
Molecular biology
Immunoglobulin A
3. Good health
Cell biology
Enzyme Activation
Immunoglobulin Isotypes
Immunoglobulin M
Ribonucleoproteins
Host-Pathogen Interactions
Humoral immunity
biology.protein
Antibody
TRIM21
Protein Binding
Fc-receptor
030215 immunology
Subjects
Details
- ISSN :
- 1600065X and 01052896
- Volume :
- 268
- Database :
- OpenAIRE
- Journal :
- Immunological Reviews
- Accession number :
- edsair.doi.dedup.....1e88cf5120fb0945c6bbea425938578d