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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Format: | Article |
Language: | English |
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Frontiers Media S.A.
2019-12-01
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Series: | Frontiers in Immunology |
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Online Access: | https://www.frontiersin.org/article/10.3389/fimmu.2019.02908/full |
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Article |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
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 |
work_keys_str_mv |
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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 |