Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response

The induction of specific and sustainable tolerance is a challenging issue in organ transplantation. The discovery of the immunosuppressive properties of apoptotic cells in animal models has paved the way for their use in human transplantation. In this work, we aimed to define a stable, reproducible...

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Main Authors: Caroline Pilon, Thomas Stehlé, Asma Beldi-Ferchiou, Marie Matignon, Allan Thiolat, Aude Burlion, Cynthia Grondin, Brigitte Birebent, France Pirenne, Hélène Rouard, Philippe Lang, Gilles Marodon, Philippe Grimbert, José L. Cohen
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.02908/full
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author Caroline Pilon
Caroline Pilon
Caroline Pilon
Thomas Stehlé
Thomas Stehlé
Thomas Stehlé
Asma Beldi-Ferchiou
Asma Beldi-Ferchiou
Marie Matignon
Marie Matignon
Marie Matignon
Marie Matignon
Allan Thiolat
Allan Thiolat
Aude Burlion
Cynthia Grondin
Cynthia Grondin
Cynthia Grondin
Brigitte Birebent
France Pirenne
France Pirenne
Hélène Rouard
Philippe Lang
Philippe Lang
Philippe Lang
Gilles Marodon
Philippe Grimbert
Philippe Grimbert
Philippe Grimbert
Philippe Grimbert
José L. Cohen
José L. Cohen
José L. Cohen
spellingShingle Caroline Pilon
Caroline Pilon
Caroline Pilon
Thomas Stehlé
Thomas Stehlé
Thomas Stehlé
Asma Beldi-Ferchiou
Asma Beldi-Ferchiou
Marie Matignon
Marie Matignon
Marie Matignon
Marie Matignon
Allan Thiolat
Allan Thiolat
Aude Burlion
Cynthia Grondin
Cynthia Grondin
Cynthia Grondin
Brigitte Birebent
France Pirenne
France Pirenne
Hélène Rouard
Philippe Lang
Philippe Lang
Philippe Lang
Gilles Marodon
Philippe Grimbert
Philippe Grimbert
Philippe Grimbert
Philippe Grimbert
José L. Cohen
José L. Cohen
José L. Cohen
Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response
Frontiers in Immunology
tolerance
NSG mice
immunomodulation
transplantation
apoptotic cell
author_facet Caroline Pilon
Caroline Pilon
Caroline Pilon
Thomas Stehlé
Thomas Stehlé
Thomas Stehlé
Asma Beldi-Ferchiou
Asma Beldi-Ferchiou
Marie Matignon
Marie Matignon
Marie Matignon
Marie Matignon
Allan Thiolat
Allan Thiolat
Aude Burlion
Cynthia Grondin
Cynthia Grondin
Cynthia Grondin
Brigitte Birebent
France Pirenne
France Pirenne
Hélène Rouard
Philippe Lang
Philippe Lang
Philippe Lang
Gilles Marodon
Philippe Grimbert
Philippe Grimbert
Philippe Grimbert
Philippe Grimbert
José L. Cohen
José L. Cohen
José L. Cohen
author_sort Caroline Pilon
title Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response
title_short Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response
title_full Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response
title_fullStr Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response
title_full_unstemmed Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune Response
title_sort human apoptotic cells, generated by extracorporeal photopheresis, modulate allogeneic immune response
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-12-01
description The induction of specific and sustainable tolerance is a challenging issue in organ transplantation. The discovery of the immunosuppressive properties of apoptotic cells in animal models has paved the way for their use in human transplantation. In this work, we aimed to define a stable, reproducible, and clinically compatible production procedure of human apoptotic cells (Apo-cells). Using a clinically approved extracorporeal photopheresis technique, we have produced and characterized phenotypically and functionally human apoptotic cells. These Apo-cells have immunosuppressive properties proved in vitro and in vivo in NOD/SCID/γC mice by their capacity to modulate an allogeneic response following both a direct and an indirect antigen presentation. These results brought the rationale for the use of Apo-cells in tolerance induction protocol for organ transplantation.
topic tolerance
NSG mice
immunomodulation
transplantation
apoptotic cell
url https://www.frontiersin.org/article/10.3389/fimmu.2019.02908/full
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spelling doaj-7c0456869ece4997a8800832fa68e86d2020-11-25T00:39:06ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-12-011010.3389/fimmu.2019.02908484500Human Apoptotic Cells, Generated by Extracorporeal Photopheresis, Modulate Allogeneic Immune ResponseCaroline Pilon0Caroline Pilon1Caroline Pilon2Thomas Stehlé3Thomas Stehlé4Thomas Stehlé5Asma Beldi-Ferchiou6Asma Beldi-Ferchiou7Marie Matignon8Marie Matignon9Marie Matignon10Marie Matignon11Allan Thiolat12Allan Thiolat13Aude Burlion14Cynthia Grondin15Cynthia Grondin16Cynthia Grondin17Brigitte Birebent18France Pirenne19France Pirenne20Hélène Rouard21Philippe Lang22Philippe Lang23Philippe Lang24Gilles Marodon25Philippe Grimbert26Philippe Grimbert27Philippe Grimbert28Philippe Grimbert29José L. Cohen30José L. Cohen31José L. Cohen32Assistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Centre d'Investigation Clinique Biothérapie, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceAssistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Centre d'Investigation Clinique Biothérapie, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceAP-HP, Groupe Hospitalo-Universitaire Chenevier Mondor, Service de Néphrologie-Transplantation, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceAssistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Centre d'Investigation Clinique Biothérapie, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceAP-HP, Groupe Hospitalo-Universitaire Chenevier Mondor, Service de Néphrologie-Transplantation, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceSorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, FranceAssistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Centre d'Investigation Clinique Biothérapie, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceEtablissement Français du Sang (EFS) – Ile de France, Créteil, FranceEtablissement Français du Sang (EFS) – Ile de France, Créteil, FranceInserm, U955, Equipe 2, Créteil, FranceEtablissement Français du Sang (EFS) – Ile de France, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceAP-HP, Groupe Hospitalo-Universitaire Chenevier Mondor, Service de Néphrologie-Transplantation, Créteil, FranceSorbonne Universités, UPMC Univ Paris 06, INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, FranceAssistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Centre d'Investigation Clinique Biothérapie, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceAP-HP, Groupe Hospitalo-Universitaire Chenevier Mondor, Service de Néphrologie-Transplantation, Créteil, FranceAssistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalo-Universitaire Chenevier Mondor, Centre d'Investigation Clinique Biothérapie, Créteil, FranceInstitut Mondor de recherche biomédicale, Université Paris-Est, UMR_S955, UPEC, Créteil, FranceInserm, U955, Equipe 21, Créteil, FranceThe induction of specific and sustainable tolerance is a challenging issue in organ transplantation. The discovery of the immunosuppressive properties of apoptotic cells in animal models has paved the way for their use in human transplantation. In this work, we aimed to define a stable, reproducible, and clinically compatible production procedure of human apoptotic cells (Apo-cells). Using a clinically approved extracorporeal photopheresis technique, we have produced and characterized phenotypically and functionally human apoptotic cells. These Apo-cells have immunosuppressive properties proved in vitro and in vivo in NOD/SCID/γC mice by their capacity to modulate an allogeneic response following both a direct and an indirect antigen presentation. These results brought the rationale for the use of Apo-cells in tolerance induction protocol for organ transplantation.https://www.frontiersin.org/article/10.3389/fimmu.2019.02908/fulltoleranceNSG miceimmunomodulationtransplantationapoptotic cell