Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells

Transplantation of allogeneic human embryonic stem cell-derived cardiac progenitors triggers an immune response. We assessed whether this response could be modulated by the concomitant use of adipose-derived stromal cells (ADSC). Peripheral blood mononuclear cells were collected from 40 patients wit...

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Main Authors: Calderon, Damelys, Planat-Benard, Valérie, Bellamy, Valérie, Vanneaux, Valérie, Kuhn, Chantal, Peyrard, Severine, Larghero, Jéröome, Desnos, Michel, Casteilla, Louis, Pucéat, Michel, Menasché, Philippe, Chatenoud, Lucienne
Format: Online
Language:English
Published: Blackwell Publishing Ltd 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823222/
id pubmed-3823222
recordtype oai_dc
spelling pubmed-38232222015-03-27 Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells Calderon, Damelys Planat-Benard, Valérie Bellamy, Valérie Vanneaux, Valérie Kuhn, Chantal Peyrard, Severine Larghero, Jéröome Desnos, Michel Casteilla, Louis Pucéat, Michel Menasché, Philippe Chatenoud, Lucienne Original Articles Transplantation of allogeneic human embryonic stem cell-derived cardiac progenitors triggers an immune response. We assessed whether this response could be modulated by the concomitant use of adipose-derived stromal cells (ADSC). Peripheral blood mononuclear cells were collected from 40 patients with coronary artery disease (CAD) and nine healthy controls. Cardiac progenitors (CD15+ Mesp1+) were generated as already reported from the I6 cell line treated with bone morphogenetic protein (BMP)-2. Adipose-derived stromal cells were obtained from abdominal dermolipectomies. We assessed the proliferative response of peripheral lymphocytes from patients and controls to cardiac progenitors cultured on a monolayer of ADSC, to allogeneic lymphocytes in mixed lymphocyte culture and to the T cell mitogen phytohemaglutin A in presence or absence of ADSC. Cardiac progenitors cultured on a monolayer of ADSC triggered a proliferation of lymphocytes from both patients and controls albeit lower than that induced by allogeneic lymphocytes. When cultured alone, ADSC did not induce any proliferation of allogeneic lymphocytes. When added to cultures of lymphocytes, ADSC significantly inhibited the alloantigen or mitogen-induced proliferative response. Compared to healthy controls, lymphocytes from patients presenting CAD expressed a decreased proliferative capacity, in particular to mitogen-induced stimulation. Adipose-derived stromal cells express an immunomodulatory effect that limits both alloantigen and mitogen-induced lymphocyte responses. Furthermore, lymphocytes from patients with CAD are low responders to conventional stimuli, possibly because of their age and disease-associated treatment regimens. We propose that, in combination, these factors may limit the in vivo immunogenicity of cardiac progenitors co-implanted with ADSC in patients with CAD. Blackwell Publishing Ltd 2012-07 2012-06-28 /pmc/articles/PMC3823222/ /pubmed/21895965 http://dx.doi.org/10.1111/j.1582-4934.2011.01435.x Text en Copyright © 2012 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Calderon, Damelys
Planat-Benard, Valérie
Bellamy, Valérie
Vanneaux, Valérie
Kuhn, Chantal
Peyrard, Severine
Larghero, Jéröome
Desnos, Michel
Casteilla, Louis
Pucéat, Michel
Menasché, Philippe
Chatenoud, Lucienne
spellingShingle Calderon, Damelys
Planat-Benard, Valérie
Bellamy, Valérie
Vanneaux, Valérie
Kuhn, Chantal
Peyrard, Severine
Larghero, Jéröome
Desnos, Michel
Casteilla, Louis
Pucéat, Michel
Menasché, Philippe
Chatenoud, Lucienne
Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
author_facet Calderon, Damelys
Planat-Benard, Valérie
Bellamy, Valérie
Vanneaux, Valérie
Kuhn, Chantal
Peyrard, Severine
Larghero, Jéröome
Desnos, Michel
Casteilla, Louis
Pucéat, Michel
Menasché, Philippe
Chatenoud, Lucienne
author_sort Calderon, Damelys
title Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
title_short Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
title_full Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
title_fullStr Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
title_full_unstemmed Immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
title_sort immune response to human embryonic stem cell-derived cardiac progenitors and adipose-derived stromal cells
description Transplantation of allogeneic human embryonic stem cell-derived cardiac progenitors triggers an immune response. We assessed whether this response could be modulated by the concomitant use of adipose-derived stromal cells (ADSC). Peripheral blood mononuclear cells were collected from 40 patients with coronary artery disease (CAD) and nine healthy controls. Cardiac progenitors (CD15+ Mesp1+) were generated as already reported from the I6 cell line treated with bone morphogenetic protein (BMP)-2. Adipose-derived stromal cells were obtained from abdominal dermolipectomies. We assessed the proliferative response of peripheral lymphocytes from patients and controls to cardiac progenitors cultured on a monolayer of ADSC, to allogeneic lymphocytes in mixed lymphocyte culture and to the T cell mitogen phytohemaglutin A in presence or absence of ADSC. Cardiac progenitors cultured on a monolayer of ADSC triggered a proliferation of lymphocytes from both patients and controls albeit lower than that induced by allogeneic lymphocytes. When cultured alone, ADSC did not induce any proliferation of allogeneic lymphocytes. When added to cultures of lymphocytes, ADSC significantly inhibited the alloantigen or mitogen-induced proliferative response. Compared to healthy controls, lymphocytes from patients presenting CAD expressed a decreased proliferative capacity, in particular to mitogen-induced stimulation. Adipose-derived stromal cells express an immunomodulatory effect that limits both alloantigen and mitogen-induced lymphocyte responses. Furthermore, lymphocytes from patients with CAD are low responders to conventional stimuli, possibly because of their age and disease-associated treatment regimens. We propose that, in combination, these factors may limit the in vivo immunogenicity of cardiac progenitors co-implanted with ADSC in patients with CAD.
publisher Blackwell Publishing Ltd
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823222/
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