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  4. Trogocytosis between Non-Immune Cells for Cell Clearance, and among Immune-Related Cells for Modulating Immune Responses and Autoimmunity
 
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Trogocytosis between Non-Immune Cells for Cell Clearance, and among Immune-Related Cells for Modulating Immune Responses and Autoimmunity

Journal
International journal of molecular sciences
Journal Volume
22
Journal Issue
5
Pages
2236
Date Issued
2021-02-24
Author(s)
KO-JEN LI  
CHENG-HAN WU  
CHENG-HSUN LU  
CHIEH-YU SHEN  
YU-MIN KUO  
Tsai, Chang-Youh
SONG-CHOU HSIEH  
CHIA-LI YU  
DOI
10.3390/ijms22052236
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/593930
URL
https://scholars.lib.ntu.edu.tw/handle/123456789/592275
Abstract
The term trogocytosis refers to a rapid bidirectional and active transfer of surface membrane fragment and associated proteins between cells. The trogocytosis requires cell-cell contact, and exhibits fast kinetics and the limited lifetime of the transferred molecules on the surface of the acceptor cells. The biological actions of trogocytosis include information exchange, cell clearance of unwanted tissues in embryonic development, immunoregulation, cancer surveillance/evasion, allogeneic cell survival and infectious pathogen killing or intercellular transmission. In the present review, we will extensively review all these aspects. In addition to its biological significance, aberrant trogocytosis in the immune system leading to autoimmunity and immune-mediated inflammatory diseases will also be discussed. Finally, the prospective investigations for further understanding the molecular basis of trogocytosis and its clinical applications will also be proposed.
Subjects
amoebic trogocytosis, cell clearance; antibody-dependent cell-mediated cytotoxicity; antigen modification; chimeric antigen receptor T lymphocyte; immune plasticity; oncologic trogocytosis; trogocytosis; tumor evasion; tumor surveillance
Amoebic trogocytosis, cell clearance; Antibody-dependent cell-mediated cytotoxicity; Antigen modification; Chimeric antigen receptor T lymphocyte; Immune plasticity; Oncologic trogocytosis; Trogocytosis; Tumor evasion; Tumor surveillance
SDGs

[SDGs]SDG3

Other Subjects
APC protein; cancer antibody; CD47 antigen; epratuzumab; HLA G antigen; immunomodulating agent; veltuzumab; allergic reaction; allograft; allotransplantation; amoeba (life cycle stage); antibody dependent cellular cytotoxicity; autoimmune disease; autoimmunity; autoinflammatory disease; basophil; CD8+ T lymphocyte; cell clearance; cell function; cell heterogeneity; cell killing; cell membrane transport; cell plasticity; cytopathogenic effect; cytotoxic T lymphocyte; dendritic cell; embryo; embryo cell; embryo development; germ cell; graft survival; human; immune evasion; immune response; immunocompetent cell; immunomodulation; immunosuppressive treatment; immunosurveillance; infectious agent; inflammation; innate immunity; mesenchymal stroma cell; natural killer cell; nonhuman; opsonization; Review; systemic lupus erythematosus; T lymphocyte; Th2 cell; trogocytosis; tumor cell; tumor immunity; tumor microenvironment; animal; antigen presentation; autoimmunity; cell communication; cell membrane; immune system; immunology; lymphocyte; lymphocyte activation; Animals; Antigen Presentation; Autoimmunity; Cell Communication; Cell Membrane; Humans; Immune System; Lymphocyte Activation; Lymphocytes
Publisher
MDPI
Type
journal article

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