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      Monitoring T-Cell Responses in Translational Studies: Optimization of Dye-Based Proliferation Assay for Evaluation of Antigen-Specific Responses

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          Abstract

          Adoptive therapy with regulatory T cells or tolerance-inducing antigen (Ag)-presenting cells is innovative and promising therapeutic approach to control undesired and harmful activation of the immune system, as observed in autoimmune diseases, solid organ and bone marrow transplantation. One of the critical issues to elucidate the mechanisms responsible for success or failure of these therapies and define the specificity of the therapy is the evaluation of the Ag-specific T-cell responses. Several efforts have been made to develop suitable and reproducible assays. Here, we focus on dye-based proliferation assays. We highlight with practical examples the fundamental issues to take into consideration for implementation of an effective and sensitive dye-based proliferation assay to monitor Ag-specific responses in patients. The most critical points were used to design a road map to set up and analyze the optimal assay to assess Ag-specific T-cell responses in patients undergoing different treatments. This is the first step to optimize monitoring of tolerance induction, allowing comparison of outcomes of different clinical studies. The road map can also be applied to other therapeutic interventions, not limited to tolerance induction therapies, in which Ag-specific T-cell responses are relevant such as vaccination approaches and cancer immunotherapy.

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          Phenotypic analysis of antigen-specific T lymphocytes.

          Identification and characterization of antigen-specific T lymphocytes during the course of an immune response is tedious and indirect. To address this problem, the peptide-major histocompatability complex (MHC) ligand for a given population of T cells was multimerized to make soluble peptide-MHC tetramers. Tetramers of human lymphocyte antigen A2 that were complexed with two different human immunodeficiency virus (HIV)-derived peptides or with a peptide derived from influenza A matrix protein bound to peptide-specific cytotoxic T cells in vitro and to T cells from the blood of HIV-infected individuals. In general, tetramer binding correlated well with cytotoxicity assays. This approach should be useful in the analysis of T cells specific for infectious agents, tumors, and autoantigens.
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            Differentiation of type 1 T regulatory cells (Tr1) by tolerogenic DC-10 requires the IL-10-dependent ILT4/HLA-G pathway.

            Type 1 T regulatory (Tr1) cells suppress immune responses in vivo and in vitro and play a key role in maintaining tolerance to self- and non-self-antigens. Interleukin-10 (IL-10) is the crucial driving factor for Tr1 cell differentiation, but the molecular mechanisms underlying this induction remain unknown. We identified and characterized a subset of IL-10-producing human dendritic cells (DCs), termed DC-10, which are present in vivo and can be induced in vitro in the presence of IL-10. DC-10 are CD14(+), CD16(+), CD11c(+), CD11b(+), HLA-DR(+), CD83(+), CD1a(-), CD1c(-), express the Ig-like transcripts (ILTs) ILT2, ILT3, ILT4, and HLA-G antigen, display high levels of CD40 and CD86, and up-regulate CD80 after differentiation in vitro. DC-10 isolated from peripheral blood or generated in vitro are potent inducers of antigen-specific IL-10-producing Tr1 cells. Induction of Tr1 cells by DC-10 is IL-10-dependent and requires the ILT4/HLA-G signaling pathway. Our data indicate that DC-10 represents a novel subset of tolerogenic DCs, which secrete high levels of IL-10, express ILT4 and HLA-G, and have the specific function to induce Tr1 cells.
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              Development of a cross-platform biomarker signature to detect renal transplant tolerance in humans.

              Identifying transplant recipients in whom immunological tolerance is established or is developing would allow an individually tailored approach to their posttransplantation management. In this study, we aimed to develop reliable and reproducible in vitro assays capable of detecting tolerance in renal transplant recipients. Several biomarkers and bioassays were screened on a training set that included 11 operationally tolerant renal transplant recipients, recipient groups following different immunosuppressive regimes, recipients undergoing chronic rejection, and healthy controls. Highly predictive assays were repeated on an independent test set that included 24 tolerant renal transplant recipients. Tolerant patients displayed an expansion of peripheral blood B and NK lymphocytes, fewer activated CD4+ T cells, a lack of donor-specific antibodies, donor-specific hyporesponsiveness of CD4+ T cells, and a high ratio of forkhead box P3 to alpha-1,2-mannosidase gene expression. Microarray analysis further revealed in tolerant recipients a bias toward differential expression of B cell-related genes and their associated molecular pathways. By combining these indices of tolerance as a cross-platform biomarker signature, we were able to identify tolerant recipients in both the training set and the test set. This study provides an immunological profile of the tolerant state that, with further validation, should inform and shape drug-weaning protocols in renal transplant recipients.
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                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/163004
                URI : http://frontiersin.org/people/u/430989
                URI : http://frontiersin.org/people/u/507606
                URI : http://frontiersin.org/people/u/505677
                URI : http://frontiersin.org/people/u/482549
                URI : http://frontiersin.org/people/u/86894
                URI : http://frontiersin.org/people/u/59452
                URI : http://frontiersin.org/people/u/507199
                URI : http://frontiersin.org/people/u/449119
                URI : http://frontiersin.org/people/u/177433
                URI : http://frontiersin.org/people/u/119865
                URI : http://frontiersin.org/people/u/507208
                URI : http://frontiersin.org/people/u/24831
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                21 December 2017
                2017
                : 8
                : 1870
                Affiliations
                [1] 1Department of Immunopathology, Sanquin Research , Amsterdam, Netherlands
                [2] 2Landsteiner Laboratory, Academic Medical Centre, University of Amsterdam , Amsterdam, Netherlands
                [3] 3Laboratory of Immunoregulation and Cellular Therapies, Department of Family Medicine, Medical University of Gdańsk , Gdańsk, Poland
                [4] 4Immunology Division, Department of Cellular Biology, Germans Trias i Pujol University Hospital and Research Institute, Physiology, and Immunology, Universitat Autònoma Barcelona , Barcelona, Spain
                [5] 5Department of Clinical Immunology and Transplantology, Medical University of Gdańsk , Gdańsk, Poland
                [6] 6San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Division of Regenerative Medicine, Stem Cells and Gene Therapy, IRCCS San Raffaele Scientific Institute , Milan, Italy
                [7] 7MRC Centre for Transplantation, King’s College London , London, United Kingdom
                Author notes

                Edited by: John Isaacs, Newcastle University, United Kingdom

                Reviewed by: Thomas Wekerle, Medical University of Vienna, Austria; Milica Vukmanovic-stejic, University College London, United Kingdom

                *Correspondence: Anja Ten Brinke, a.tenbrinke@ 123456sanquin.nl

                Present address: Maria P. Hernandez-Fuentes, UCB Pharma, Slough, United Kingdom

                Specialty section: This article was submitted to Immunological Tolerance and Regulation, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2017.01870
                5742609
                29312346
                37c71fe3-1c2b-4620-a047-c9674f0611be
                Copyright © 2017 Ten Brinke, Marek-Trzonkowska, Mansilla, Turksma, Piekarska, Iwaszkiewicz-Grześ, Passerini, Locafaro, Puñet-Ortiz, van Ham, Hernandez-Fuentes, Martínez-Cáceres and Gregori.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 23 August 2017
                : 08 December 2017
                Page count
                Figures: 7, Tables: 0, Equations: 0, References: 46, Pages: 15, Words: 10366
                Categories
                Immunology
                Protocols

                Immunology
                tolerance,monitoring,proliferation,antigen-specific,t cells,transplantation,autoimmune diseases,immune-therapies

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