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Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis

Haematopoietic stem cell transplantation currently remains the only curative treatment of primary forms of haemophagocytic lymphohistiocytosis (HLH). Rapid diagnosis, efficient primary treatment of hyperinflammation, and conditioning regimens tailored to this demanding condition have substantially i...

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Detalles Bibliográficos
Autores principales: Lehmberg, Kai, Moshous, Despina, Booth, Claire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823612/
https://www.ncbi.nlm.nih.gov/pubmed/31709205
http://dx.doi.org/10.3389/fped.2019.00435
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author Lehmberg, Kai
Moshous, Despina
Booth, Claire
author_facet Lehmberg, Kai
Moshous, Despina
Booth, Claire
author_sort Lehmberg, Kai
collection PubMed
description Haematopoietic stem cell transplantation currently remains the only curative treatment of primary forms of haemophagocytic lymphohistiocytosis (HLH). Rapid diagnosis, efficient primary treatment of hyperinflammation, and conditioning regimens tailored to this demanding condition have substantially improved prognosis in the past 40 years. However, refractory hyperinflammation, central nervous system (CNS) involvement, unavailability of matched donors, susceptibility to conditioning-related toxicities, and a high frequency of mixed chimaerism remain a challenge in a substantial proportion of patients. Gene therapeutic approaches for several genetic defects of primary HLH are being developed at pre-clinical and translational levels.
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spelling pubmed-68236122019-11-08 Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis Lehmberg, Kai Moshous, Despina Booth, Claire Front Pediatr Pediatrics Haematopoietic stem cell transplantation currently remains the only curative treatment of primary forms of haemophagocytic lymphohistiocytosis (HLH). Rapid diagnosis, efficient primary treatment of hyperinflammation, and conditioning regimens tailored to this demanding condition have substantially improved prognosis in the past 40 years. However, refractory hyperinflammation, central nervous system (CNS) involvement, unavailability of matched donors, susceptibility to conditioning-related toxicities, and a high frequency of mixed chimaerism remain a challenge in a substantial proportion of patients. Gene therapeutic approaches for several genetic defects of primary HLH are being developed at pre-clinical and translational levels. Frontiers Media S.A. 2019-10-25 /pmc/articles/PMC6823612/ /pubmed/31709205 http://dx.doi.org/10.3389/fped.2019.00435 Text en Copyright © 2019 Lehmberg, Moshous and Booth. 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) and the copyright owner(s) 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 Pediatrics
Lehmberg, Kai
Moshous, Despina
Booth, Claire
Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
title Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
title_full Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
title_fullStr Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
title_full_unstemmed Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
title_short Haematopoietic Stem Cell Transplantation for Primary Haemophagocytic Lymphohistiocytosis
title_sort haematopoietic stem cell transplantation for primary haemophagocytic lymphohistiocytosis
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6823612/
https://www.ncbi.nlm.nih.gov/pubmed/31709205
http://dx.doi.org/10.3389/fped.2019.00435
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