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1.
Nat Immunol ; 20(2): 218-231, 2019 02.
Article in English | MEDLINE | ID: mdl-30643268

ABSTRACT

Regulatory T cells (Treg cells) can activate multiple suppressive mechanisms in vitro after activation via the T cell antigen receptor, resulting in antigen-independent suppression. However, it remains unclear whether similar pathways operate in vivo. Here we found that antigen-specific Treg cells activated by dendritic cells (DCs) pulsed with two antigens suppressed conventional naive T cells (Tnaive cells) specific for both cognate antigens and non-cognate antigens in vitro but suppressed only Tnaive cells specific for cognate antigen in vivo. Antigen-specific Treg cells formed strong interactions with DCs, resulting in selective inhibition of the binding of Tnaive cells to cognate antigen yet allowing bystander Tnaive cell access. Strong binding resulted in the removal of the complex of cognate peptide and major histocompatibility complex class II (pMHCII) from the DC surface, reducing the capacity of DCs to present antigen. The enhanced binding of Treg cells to DCs, coupled with their capacity to deplete pMHCII, represents a novel pathway for Treg cell-mediated suppression and may be a mechanism by which Treg cells maintain immune homeostasis.


Subject(s)
Antigen Presentation/immunology , Dendritic Cells/immunology , Histocompatibility Antigens Class II/immunology , Immune Tolerance/immunology , T-Lymphocytes, Regulatory/immunology , Animals , Bystander Effect/immunology , Cells, Cultured , Lymphocyte Activation/immunology , Mice , Mice, Inbred C57BL , Mice, Transgenic , Peptides/immunology , Primary Cell Culture , Receptors, Antigen, T-Cell/genetics , Receptors, Antigen, T-Cell/immunology , Receptors, Antigen, T-Cell/metabolism , T-Lymphocytes, Regulatory/metabolism
2.
J Immunol Methods ; 441: 67-71, 2017 02.
Article in English | MEDLINE | ID: mdl-27919837

ABSTRACT

Ex-vivo differentiation of regulatory T cells (Tregs) from naïve CD4+ T-cells has been widely used in immunological research. Isolation of a highly pure naïve T cell population is the key factor that determines the efficiency of subsequent Treg differentiation. Currently, this step relies mostly on FACS sorting, which is often costly, time consuming, and inconvenient. Alternatively, magnetic separation of T-cells can be performed; yet, available protocols fail to reach sort level purity and consequently result in low Treg differentiation efficiency. Here, we present the results of a comprehensive side-by-side comparison of various magnetic separation strategies and FACS sorting in multiple levels. Additionally, we propose a novel optimized custom made magnetic separation protocol, which not only yields sort level purity and Treg differentiation but also lowers the reagent costs up to 75% compared to the commercially available purification kits. The highly pure naïve CD4+ T-cell population obtained by this versatile method can also be used for differentiation of other T-cell subsets; therefore this protocol may have broad applications in T-cell research.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Cell Separation/methods , T-Lymphocytes, Regulatory/immunology , Cell Differentiation , Flow Cytometry/methods , Humans , Immunomagnetic Separation , Lymphocyte Activation , T-Lymphocyte Subsets/immunology
3.
J Immunol ; 197(5): 2027-38, 2016 09 01.
Article in English | MEDLINE | ID: mdl-27439517

ABSTRACT

Barcoding of biological samples is a commonly used strategy to mark or identify individuals within a complex mixture. However, cell barcoding has not yet found wide use in flow cytometry that would benefit greatly from the ability to analyze pooled experimental samples simultaneously. This is due, in part, to technical and practical limitations of current fluorescent dye-based methods. In this study, we describe a simple, versatile barcoding strategy that relies on combinations of a single Ab conjugated to different fluorochromes and thus in principle can be integrated into any flow cytometry application. To demonstrate the efficacy of the approach, we describe the results of a variety of experiments using live cells as well as fixed and permeabilized cells. The results of these studies show that Ab-based barcoding provides a simple, practical method for identifying cells from individual samples pooled for analysis by flow cytometry that has broad applications in immunological research.


Subject(s)
Antibodies/isolation & purification , Electronic Data Processing/methods , Flow Cytometry/methods , Animals , Antibodies/chemistry , Antibodies/classification , Fluorescent Dyes/chemistry , Humans , Mice , Staining and Labeling
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