CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation.
Immune recovery after profound lymphopenia is a major challenge in many clinical situations, such as allogeneic hematopoietic stem cell transplantation (allo-HSCT). Recovery depends, in a first step, on hematopoietic lymphoid progenitors production in the bone marrow (BM). In this study, we characte...
Guardado en:
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2014
|
Materias: | |
Acceso en línea: | https://doaj.org/article/70eac6067aef47979fdab7b3122e8929 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:70eac6067aef47979fdab7b3122e8929 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:70eac6067aef47979fdab7b3122e89292021-11-18T08:28:31ZCXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation.1932-620310.1371/journal.pone.0091492https://doaj.org/article/70eac6067aef47979fdab7b3122e89292014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24621606/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Immune recovery after profound lymphopenia is a major challenge in many clinical situations, such as allogeneic hematopoietic stem cell transplantation (allo-HSCT). Recovery depends, in a first step, on hematopoietic lymphoid progenitors production in the bone marrow (BM). In this study, we characterized CD34+Lin-CD10+ lymphoid progenitors in the peripheral blood of allo-HSCT patients. Our data demonstrate a strong recovery of this population 3 months after transplantation. This rebound was abolished in patients who developed acute graft-versus-host disease (aGVHD). A similar recovery profile was found for both CD24+ and CD24- progenitor subpopulations. CD34+lin-CD10+CD24- lymphoid progenitors sorted from allo-HSCT patients preserved their T cell potentiel according to in vitro T-cell differentiation assay and the expression profile of 22 genes involved in T-cell differentiation and homing. CD34+lin-CD10+CD24- cells from patients without aGVHD had reduced CXCR4 gene expression, consistent with an enhanced egress from the BM. CCR7 gene expression was reduced in patients after allo-HSCT, as were its ligands CCL21 and CCL19. This reduction was particularly marked in patients with aGVHD, suggesting a possible impact on thymic homing. Thus, the data presented here identify this population as an important early step in T cell reconstitution in humans and so, an important target when seeking to enhance immune reconstitution.Salomé GlauzyIsabelle André-SchmutzJérôme LargheroSophie EzineRégis Peffault de LatourHélène Moins-TeisserencSophie ServaisMarie RobinGérard SociéEmmanuel ClaveAntoine ToubertPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 3, p e91492 (2014) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Salomé Glauzy Isabelle André-Schmutz Jérôme Larghero Sophie Ezine Régis Peffault de Latour Hélène Moins-Teisserenc Sophie Servais Marie Robin Gérard Socié Emmanuel Clave Antoine Toubert CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
description |
Immune recovery after profound lymphopenia is a major challenge in many clinical situations, such as allogeneic hematopoietic stem cell transplantation (allo-HSCT). Recovery depends, in a first step, on hematopoietic lymphoid progenitors production in the bone marrow (BM). In this study, we characterized CD34+Lin-CD10+ lymphoid progenitors in the peripheral blood of allo-HSCT patients. Our data demonstrate a strong recovery of this population 3 months after transplantation. This rebound was abolished in patients who developed acute graft-versus-host disease (aGVHD). A similar recovery profile was found for both CD24+ and CD24- progenitor subpopulations. CD34+lin-CD10+CD24- lymphoid progenitors sorted from allo-HSCT patients preserved their T cell potentiel according to in vitro T-cell differentiation assay and the expression profile of 22 genes involved in T-cell differentiation and homing. CD34+lin-CD10+CD24- cells from patients without aGVHD had reduced CXCR4 gene expression, consistent with an enhanced egress from the BM. CCR7 gene expression was reduced in patients after allo-HSCT, as were its ligands CCL21 and CCL19. This reduction was particularly marked in patients with aGVHD, suggesting a possible impact on thymic homing. Thus, the data presented here identify this population as an important early step in T cell reconstitution in humans and so, an important target when seeking to enhance immune reconstitution. |
format |
article |
author |
Salomé Glauzy Isabelle André-Schmutz Jérôme Larghero Sophie Ezine Régis Peffault de Latour Hélène Moins-Teisserenc Sophie Servais Marie Robin Gérard Socié Emmanuel Clave Antoine Toubert |
author_facet |
Salomé Glauzy Isabelle André-Schmutz Jérôme Larghero Sophie Ezine Régis Peffault de Latour Hélène Moins-Teisserenc Sophie Servais Marie Robin Gérard Socié Emmanuel Clave Antoine Toubert |
author_sort |
Salomé Glauzy |
title |
CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
title_short |
CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
title_full |
CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
title_fullStr |
CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
title_full_unstemmed |
CXCR4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
title_sort |
cxcr4-related increase of circulating human lymphoid progenitors after allogeneic hematopoietic stem cell transplantation. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2014 |
url |
https://doaj.org/article/70eac6067aef47979fdab7b3122e8929 |
work_keys_str_mv |
AT salomeglauzy cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT isabelleandreschmutz cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT jeromelarghero cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT sophieezine cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT regispeffaultdelatour cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT helenemoinsteisserenc cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT sophieservais cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT marierobin cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT gerardsocie cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT emmanuelclave cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation AT antoinetoubert cxcr4relatedincreaseofcirculatinghumanlymphoidprogenitorsafterallogeneichematopoieticstemcelltransplantation |
_version_ |
1718421747850543104 |