Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis

Systemic Sclerosis (SSc) is a complex autoimmune disease, characterized by high mortality and morbidity. The heterogeneity in terms of extent, severity, and rate of progression of skin and internal organ involvement gives rise to many difficulties in finding the optimal therapeutic interventions for...

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Main Authors: Nicoletta Del Papa, Francesca Pignataro, Eleonora Zaccara, Wanda Maglione, Antonina Minniti
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-10-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.02390/full
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spelling doaj-03ed0c39b0a84edcaaa4f3d96a7762032020-11-25T01:56:31ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-10-01910.3389/fimmu.2018.02390409306Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic SclerosisNicoletta Del PapaFrancesca PignataroEleonora ZaccaraWanda MaglioneAntonina MinnitiSystemic Sclerosis (SSc) is a complex autoimmune disease, characterized by high mortality and morbidity. The heterogeneity in terms of extent, severity, and rate of progression of skin and internal organ involvement gives rise to many difficulties in finding the optimal therapeutic interventions for SSc and, to date, no disease-modifying agents are available. In this scenario, it is not surprising that SSc was one of the first autoimmune diseases challenged with high-dose immunosuppressive treatment followed by autologous hematopoietic stem cell transplantation (AHSCT). In the last decades, AHSCT has emerged as a treatment option for refractory SSc through a reduction of the aberrant immune cells, followed by re-constitution of a new, self-tolerant immune system. After several case series and pilot studies, more recently three randomized controlled trials have shown a benefit in skin involvement, organ functions and quality of life measures in AHSCT compared to monthly cyclophosphamide. In addition, although AHSCT presents a certain risk of mortality, it has been shown that the overall survival is better, compared to the cyclophosphamide group. Current evidence suggests that SSc patients who are most likely to benefit from AHSCT are early, active, with rapidly progressing diffuse skin disease, and mild involvement of internal organs. As the studies have progressed, it has become evident the need for a more rigorous patient selection, the optimization of transplant and post-transplant procedures, and the intervention of multidisciplinary teams of specialists to increase the safety and efficacy of AHSCT in SSc.https://www.frontiersin.org/article/10.3389/fimmu.2018.02390/fullsystemic sclerosis (Scleroderma)stem cellstherapytransplantationhaematopoietic
collection DOAJ
language English
format Article
sources DOAJ
author Nicoletta Del Papa
Francesca Pignataro
Eleonora Zaccara
Wanda Maglione
Antonina Minniti
spellingShingle Nicoletta Del Papa
Francesca Pignataro
Eleonora Zaccara
Wanda Maglione
Antonina Minniti
Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis
Frontiers in Immunology
systemic sclerosis (Scleroderma)
stem cells
therapy
transplantation
haematopoietic
author_facet Nicoletta Del Papa
Francesca Pignataro
Eleonora Zaccara
Wanda Maglione
Antonina Minniti
author_sort Nicoletta Del Papa
title Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis
title_short Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis
title_full Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis
title_fullStr Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis
title_full_unstemmed Autologous Hematopoietic Stem Cell Transplantation for Treatment of Systemic Sclerosis
title_sort autologous hematopoietic stem cell transplantation for treatment of systemic sclerosis
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2018-10-01
description Systemic Sclerosis (SSc) is a complex autoimmune disease, characterized by high mortality and morbidity. The heterogeneity in terms of extent, severity, and rate of progression of skin and internal organ involvement gives rise to many difficulties in finding the optimal therapeutic interventions for SSc and, to date, no disease-modifying agents are available. In this scenario, it is not surprising that SSc was one of the first autoimmune diseases challenged with high-dose immunosuppressive treatment followed by autologous hematopoietic stem cell transplantation (AHSCT). In the last decades, AHSCT has emerged as a treatment option for refractory SSc through a reduction of the aberrant immune cells, followed by re-constitution of a new, self-tolerant immune system. After several case series and pilot studies, more recently three randomized controlled trials have shown a benefit in skin involvement, organ functions and quality of life measures in AHSCT compared to monthly cyclophosphamide. In addition, although AHSCT presents a certain risk of mortality, it has been shown that the overall survival is better, compared to the cyclophosphamide group. Current evidence suggests that SSc patients who are most likely to benefit from AHSCT are early, active, with rapidly progressing diffuse skin disease, and mild involvement of internal organs. As the studies have progressed, it has become evident the need for a more rigorous patient selection, the optimization of transplant and post-transplant procedures, and the intervention of multidisciplinary teams of specialists to increase the safety and efficacy of AHSCT in SSc.
topic systemic sclerosis (Scleroderma)
stem cells
therapy
transplantation
haematopoietic
url https://www.frontiersin.org/article/10.3389/fimmu.2018.02390/full
work_keys_str_mv AT nicolettadelpapa autologoushematopoieticstemcelltransplantationfortreatmentofsystemicsclerosis
AT francescapignataro autologoushematopoieticstemcelltransplantationfortreatmentofsystemicsclerosis
AT eleonorazaccara autologoushematopoieticstemcelltransplantationfortreatmentofsystemicsclerosis
AT wandamaglione autologoushematopoieticstemcelltransplantationfortreatmentofsystemicsclerosis
AT antoninaminniti autologoushematopoieticstemcelltransplantationfortreatmentofsystemicsclerosis
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