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Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation

The bone marrow is the origin of all hematopoietic lineages and an important homing site for memory cells of the adaptive immune system. It has recently emerged as a graft-versus-host disease (GvHD) target organ after allogeneic stem cell transplantation (alloHSCT), marked by depletion of both hemat...

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Autores principales: Szyska, Martin, Na, Il-Kang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811960/
https://www.ncbi.nlm.nih.gov/pubmed/27066008
http://dx.doi.org/10.3389/fimmu.2016.00118
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author Szyska, Martin
Na, Il-Kang
author_facet Szyska, Martin
Na, Il-Kang
author_sort Szyska, Martin
collection PubMed
description The bone marrow is the origin of all hematopoietic lineages and an important homing site for memory cells of the adaptive immune system. It has recently emerged as a graft-versus-host disease (GvHD) target organ after allogeneic stem cell transplantation (alloHSCT), marked by depletion of both hematopoietic progenitors and niche-forming cells. Serious effects on the restoration of hematopoietic function and immunological memory are common, especially in patients after myeloablative conditioning therapy. Cytopenia and durable immunodeficiency caused by the depletion of hematopoietic progenitors and destruction of bone marrow niches negatively influence the outcome of alloHSCT. The complex balance between immunosuppressive and cell-depleting treatments, GvHD and immune reconstitution, as well as the desirable graft-versus-tumor (GvT) effect remains a great challenge for clinicians.
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spelling pubmed-48119602016-04-08 Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation Szyska, Martin Na, Il-Kang Front Immunol Immunology The bone marrow is the origin of all hematopoietic lineages and an important homing site for memory cells of the adaptive immune system. It has recently emerged as a graft-versus-host disease (GvHD) target organ after allogeneic stem cell transplantation (alloHSCT), marked by depletion of both hematopoietic progenitors and niche-forming cells. Serious effects on the restoration of hematopoietic function and immunological memory are common, especially in patients after myeloablative conditioning therapy. Cytopenia and durable immunodeficiency caused by the depletion of hematopoietic progenitors and destruction of bone marrow niches negatively influence the outcome of alloHSCT. The complex balance between immunosuppressive and cell-depleting treatments, GvHD and immune reconstitution, as well as the desirable graft-versus-tumor (GvT) effect remains a great challenge for clinicians. Frontiers Media S.A. 2016-03-30 /pmc/articles/PMC4811960/ /pubmed/27066008 http://dx.doi.org/10.3389/fimmu.2016.00118 Text en Copyright © 2016 Szyska and Na. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Szyska, Martin
Na, Il-Kang
Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation
title Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation
title_full Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation
title_fullStr Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation
title_full_unstemmed Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation
title_short Bone Marrow GvHD after Allogeneic Hematopoietic Stem Cell Transplantation
title_sort bone marrow gvhd after allogeneic hematopoietic stem cell transplantation
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811960/
https://www.ncbi.nlm.nih.gov/pubmed/27066008
http://dx.doi.org/10.3389/fimmu.2016.00118
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