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Updated: Aug 18, 2026

Generation of Human Alloantigen-specific T Cells from Peripheral Blood
Published on: November 21, 2014
Microparticles shed from different antigen-presenting cells display an individual pattern of surface molecules and a
W Kolowos1, U S Gaipl, A Sheriff
1Department of Internal Medicine III, Institute for Clinical Immunology and Rheumatology, Friedrich-Alexander University of Erlangen-Nuremberg, Erlangen, Germany.
Abstract:
Various cells such as platelets, lymphocytes, endothelial cells, red blood cells and monocytes do release surface-derived microparticles (mps). We analysed mp isolated from supernatants of cultured antigen-presenting human cells (APCs) and human cell lines. Particle sizing by dynamic light scattering revealed a characteristic size of the particles ranging from 80 nm to 300 nm in viable cells and from 400 nm to 1200 nm in irradiated cells. Employing flow-cytometry, we observed partly an altered surface protein composition of the mp compared to their cellular source. Mp originating from dendritic cells (DCs) differed in their surface composition from those released from monocytes and monocyte-derived macrophages. In functional assays, these mp stimulated alloreactive T-cells. The treatment of the cells with either UV-B or lipopolysaccharide strongly influenced the quantity, the immunostimulatory features and the surface composition of the mp. Mp from apoptotic macrophages were able to reduce the stimulatory capacity of vital macrophages but not of DC. Apoptotic mps from DC, on the other hand, were always stimulatory. This is the first report regarding the study of mp released from DC and compared with those released from other APC.
Insights
Microparticles (MPs) from human antigen-presenting cells (APCs) vary in size and surface proteins. MPs from dendritic cells (DCs) and macrophages show distinct properties and immune-stimulating effects, influencing T-cell responses.
Area of Science:
- Immunology
- Cell Biology
- Biotechnology
Background:
- Cells release microparticles (MPs), which are small vesicles derived from cell surfaces.
- Antigen-presenting cells (APCs), including dendritic cells (DCs) and macrophages, are crucial for initiating immune responses.
- The characteristics and functions of MPs derived from various cell types, especially APCs, are not fully understood.
Purpose of the Study:
- To analyze the size, surface protein composition, and immunomodulatory functions of MPs derived from human APCs.
- To compare MPs from dendritic cells (DCs) with those from monocytes and macrophages.
- To investigate the impact of cellular treatments (UV-B, lipopolysaccharide) and apoptosis on MP properties.
Main Methods:
- Isolation and characterization of MPs from cultured human APCs and cell lines.
- Particle sizing using dynamic light scattering.
- Surface protein analysis using flow cytometry.
- Functional assays to assess T-cell stimulation and immunomodulatory capacity.
Main Results:
- MPs from viable APCs ranged from 80-300 nm, while MPs from irradiated cells were larger (400-1200 nm).
- MPs exhibited altered surface protein composition compared to their parent cells, with distinct profiles for DC-derived MPs versus monocyte/macrophage-derived MPs.
- MPs from DCs and macrophages demonstrated T-cell stimulatory capacity, influenced by cellular treatments and apoptotic status.
- Apoptotic macrophage MPs could suppress vital macrophage activity, whereas apoptotic DC MPs remained stimulatory.
Conclusions:
- This study provides the first comprehensive comparison of MPs released from dendritic cells (DCs) and other antigen-presenting cells (APCs).
- MP characteristics (size, surface proteins) and functions (immunostimulation) are significantly influenced by the cell of origin, cellular treatments, and apoptotic state.
- DC-derived MPs possess unique properties and potent immunostimulatory effects, highlighting their potential role in immune regulation and therapeutic applications.
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