医学
干细胞
间充质干细胞
造血
硬皮病(真菌)
再生(生物学)
造血干细胞移植
纤维化
移植
免疫学
疾病
造血干细胞
多发性硬化
癌症研究
病理
生物
内科学
细胞生物学
遗传学
接种
作者
Ensheng Xue,Antonina Minniti,Tobias Alexander,Nicoletta Del Papa,Raffaella Greco,on behalf of The Autoimmune Diseases Working Party of the EBMT
出处
期刊:Cells
[MDPI AG]
日期:2022-10-24
卷期号:11 (21): 3346-3346
被引量:4
标识
DOI:10.3390/cells11213346
摘要
Systemic sclerosis (SSc) is a systemic disease characterized by autoimmune responses, vasculopathy and tissue fibrosis. The pathogenic mechanisms involve a wide range of cells and soluble factors. The complexity of interactions leads to heterogeneous clinical features in terms of the extent, severity, and rate of progression of skin fibrosis and internal organ involvement. Available disease-modifying drugs have only modest effects on halting disease progression and may be associated with significant side effects. Therefore, cellular therapies have been developed aiming at the restoration of immunologic self-tolerance in order to provide durable remissions or to foster tissue regeneration. Currently, SSc is recommended as the 'standard indication' for autologous hematopoietic stem cell transplantation by the European Society for Blood and Marrow Transplantation. This review provides an overview on cellular therapies in SSc, from pre-clinical models to clinical applications, opening towards more advanced cellular therapies, such as mesenchymal stem cells, regulatory T cells and potentially CAR-T-cell therapies.
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