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      Hematopoietic Chimerism and Transplantation Tolerance: A Role for Regulatory T Cells

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          Abstract

          The immunosuppressive regimens currently used in transplantation to prevent allograft destruction by the host’s immune system have deleterious side effects and fail to control chronic rejection processes. Induction of donor-specific non-responsiveness (i.e., immunological tolerance) to transplants would solve these problems and would substantially ameliorate patients’ quality of life. It has been proposed that bone marrow or hematopoietic stem-cell transplantation, and resulting (mixed) hematopoietic chimerism, lead to immunological tolerance to organs of the same donor. However, a careful analysis of the literature, performed here, clearly establishes that whereas hematopoietic chimerism substantially prolongs allograft survival, it does not systematically prevent chronic rejection. Moreover, the cytotoxic conditioning regimens used to achieve long-term persistence of chimerism are associated with severe side effects that appear incompatible with a routine use in the clinic. Several laboratories recently embarked on different studies to develop alternative strategies to overcome these issues. We discuss here recent advances obtained by combining regulatory T cell infusion with bone-marrow transplantation. In experimental settings, this attractive approach allows development of genuine immunological tolerance to donor tissues using clinically relevant conditioning regimens.

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          Most cited references148

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          Dendritic Cells Induce Peripheral T Cell Unresponsiveness under Steady State Conditions in Vivo

          Dendritic cells (DCs) have the capacity to initiate immune responses, but it has been postulated that they may also be involved in inducing peripheral tolerance. To examine the function of DCs in the steady state we devised an antigen delivery system targeting these specialized antigen presenting cells in vivo using a monoclonal antibody to a DC-restricted endocytic receptor, DEC-205. Our experiments show that this route of antigen delivery to DCs is several orders of magnitude more efficient than free peptide in complete Freund's adjuvant (CFA) in inducing T cell activation and cell division. However, T cells activated by antigen delivered to DCs are not polarized to produce T helper type 1 cytokine interferon γ and the activation response is not sustained. Within 7 d the number of antigen-specific T cells is severely reduced, and the residual T cells become unresponsive to systemic challenge with antigen in CFA. Coinjection of the DC-targeted antigen and anti-CD40 agonistic antibody changes the outcome from tolerance to prolonged T cell activation and immunity. We conclude that in the absence of additional stimuli DCs induce transient antigen-specific T cell activation followed by T cell deletion and unresponsiveness.
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            CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells.

            CD40 ligand (CD40L, CD154), a transmembrane protein structurally related to the cytokine TNF-alpha, was originally identified on stimulated CD4+ T cells, and later on stimulated mast cells and basophils. Interaction of CD40L on T cells with CD40 on B cells is of paramount importance for the development and function of the humoral immune system. CD40 is not only constitutively present on B cells, but it is also found on monocytes, macrophages and endothelial cells, suggesting that CD40L has a broader function in vivo. We now report that platelets express CD40L within seconds of activation in vitro and in the process of thrombus formation in vivo. Like TNF-alpha and interleukin-1, CD40L on platelets induces endothelial cells to secrete chemokines and to express adhesion molecules, thereby generating signals for the recruitment and extravasation of leukocytes at the site of injury. Our results indicate that platelets are not only involved in haemostasis but that they also directly initiate an inflammatory response of the vessel wall.
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              In vivo imaging of Treg cells providing immune privilege to the haematopoietic stem-cell niche.

              Stem cells reside in a specialized regulatory microenvironment or niche, where they receive appropriate support for maintaining self-renewal and multi-lineage differentiation capacity. The niche may also protect stem cells from environmental insults including cytotoxic chemotherapy and perhaps pathogenic immunity. The testis, hair follicle and placenta are all sites of residence for stem cells and are immune-suppressive environments, called immune-privileged sites, where multiple mechanisms cooperate to prevent immune attack, even enabling prolonged survival of foreign allografts without immunosuppression. We sought to determine if somatic stem-cell niches more broadly are immune-privileged sites by examining the haematopoietic stem/progenitor cell (HSPC) niche in the bone marrow, a site where immune reactivity exists. We observed persistence of HSPCs from allogeneic donor mice (allo-HSPCs) in non-irradiated recipient mice for 30 days without immunosuppression with the same survival frequency compared to syngeneic HSPCs. These HSPCs were lost after the depletion of FoxP3 regulatory T (T(reg)) cells. High-resolution in vivo imaging over time demonstrated marked co-localization of HSPCs with T(reg) cells that accumulated on the endosteal surface in the calvarial and trabecular bone marrow. T(reg) cells seem to participate in creating a localized zone where HSPCs reside and where T(reg) cells are necessary for allo-HSPC persistence. In addition to processes supporting stem-cell function, the niche will provide a relative sanctuary from immune attack.
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                Author and article information

                Journal
                Front Immunol
                Front Immunol
                Front. Immun.
                Frontiers in Immunology
                Frontiers Research Foundation
                1664-3224
                28 December 2011
                2011
                : 2
                : 80
                Affiliations
                [1] 1simpleINSERM U1043 Toulouse, France
                [2] 2simpleCNRS U5282 Toulouse, France
                [3] 3simpleCentre de Physiopathologie de Toulouse Purpan, Université Paul Sabatier, Université de Toulouse Toulouse, France
                Author notes

                Edited by: Stephen Paul Cobbold, University of Oxford, UK

                Reviewed by: Stephen Paul Cobbold, University of Oxford, UK; Xian Chang Li, Brigham and Women’s Hospital, USA

                *Correspondence: Joost P. M. van Meerwijk, INSERM U1043, BP 3028, 31024 Toulouse Cedex 3, France. e-mail: joost.van-meerwijk@ 123456inserm.fr

                Present address: Olivier Joffre, INSERM U932, Institut Curie, F-75005 Paris, France.; Thibault Santolaria, INSERM U892, F-44007 Nantes, France.

                Lise Pasquet and Olivier Joffre have contributed equally to this work.

                This article was submitted to Frontiers in Immunological Tolerance, a specialty of Frontiers in Immunology.

                Article
                10.3389/fimmu.2011.00080
                3342389
                22566869
                32ab6d73-0434-4f66-b85d-dcb23079528a
                Copyright © 2011 Pasquet, Joffre, Santolaria and van Meerwijk.

                This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.

                History
                : 20 July 2011
                : 05 December 2011
                Page count
                Figures: 2, Tables: 3, Equations: 0, References: 161, Pages: 15, Words: 13116
                Categories
                Immunology
                Review Article

                Immunology
                transplantation tolerance,passive tolerance,chronic rejection,regulatoryt lymphocytes,active tolerance,hematopoietic chimerism

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