Literature DB >> 20345339

Allogenic bone-marrow-derived mesenchymal stem cells transplantation as a novel therapy for systemic lupus erythematosus.

Huayong Zhang1, Xiaofeng Zeng, Lingyun Sun.   

Abstract

IMPORTANCE OF THE FIELD: Bone-marrow-derived mesenchymal stem cells (BMMSC) are multipotent non-hematopoietic progenitor cells that are being explored as a promising new treatment for tissue regeneration. Although their immunomodulatory properties are not yet completely understood, their low immunogenic potential together with their effects on immune response make them a promising therapeutic tool for severe refractory autoimmune diseases including systemic lupus erythematosus (SLE). AREA COVERED IN THIS REVIEW: Our aim is to discuss recent progress in understanding the role of malfunctioning BMMSC in etiopathogenesis of SLE and to explore allogenic BMMSC transplantation as a potential therapy for SLE. WHAT THE READER WILL GAIN: Recent evidence suggests that the functions of BMMSC are disrupted in SLE pathology. This malfunction may result as a corollary of the disease, or may play a more fundamental role in its etiopathogenesis. We provide a brief characterization of BMMSC immunomodulatory effects, and describe our current understanding of the mechanisms by which it plays a part in treating SLE. We also present our clinical trial using allogenic BMMSC in this context. TAKE HOME MESSAGE: Allogenic BMMSC appear to be a safe therapeutic option for treatment-resistant SLE as illustrated in our clinical trial.

Entities:  

Mesh:

Year:  2010        PMID: 20345339     DOI: 10.1517/14712591003769816

Source DB:  PubMed          Journal:  Expert Opin Biol Ther        ISSN: 1471-2598            Impact factor:   4.388


  8 in total

Review 1.  The stem cell niche should be a key issue for cell therapy in regenerative medicine.

Authors:  José Becerra; Leonor Santos-Ruiz; José A Andrades; Manuel Marí-Beffa
Journal:  Stem Cell Rev Rep       Date:  2011-06       Impact factor: 5.739

Review 2.  Human stromal (mesenchymal) stem cells: basic biology and current clinical use for tissue regeneration.

Authors:  Abdullah Aldahmash; Walid Zaher; May Al-Nbaheen; Moustapha Kassem
Journal:  Ann Saudi Med       Date:  2012 Jan-Feb       Impact factor: 1.526

3.  Wnt/β-catenin signaling mediates the senescence of bone marrow-mesenchymal stem cells from systemic lupus erythematosus patients through the p53/p21 pathway.

Authors:  Zhifeng Gu; Wei Tan; Guijuan Feng; Yan Meng; Biyu Shen; Hong Liu; Chun Cheng
Journal:  Mol Cell Biochem       Date:  2013-10-16       Impact factor: 3.396

4.  Bone marrow mesenchymal stem cells suppress metastatic tumor development in mouse by modulating immune system.

Authors:  Lei Zhang; Xiao San Su; Jun Song Ye; Yi Yin Wang; Zheng Guan; Yan Feng Yin
Journal:  Stem Cell Res Ther       Date:  2015-03-24       Impact factor: 6.832

5.  Mesenchymal stromal cells attenuate sevoflurane-induced apoptosis in human neuroglioma H4 cells.

Authors:  Yanyong Cheng; Yunfeng Jiang; Lei Zhang; Jiayi Wang; Dongdong Chai; Rong Hu; Chunzhu Li; Yu Sun; Hong Jiang
Journal:  BMC Anesthesiol       Date:  2018-07-18       Impact factor: 2.217

6.  Exosomes Derived from IDO1-Overexpressing Rat Bone Marrow Mesenchymal Stem Cells Promote Immunotolerance of Cardiac Allografts.

Authors:  Ji-Gang He; Qiao-Li Xie; Bei-Bei Li; Liang Zhou; Dan Yan
Journal:  Cell Transplant       Date:  2018-10-12       Impact factor: 4.064

7.  Engraftment of donor mesenchymal stem cells in chimeric BXSB includes vascular endothelial cells and hepatocytes.

Authors:  Olcay Y Jones; Faysal Gok; Elisabeth J Rushing; Iren Horkayne-Szakaly; Atif A Ahmed
Journal:  Stem Cells Cloning       Date:  2011-12-09

8.  Mesenchymal stem cells do not prevent antibody responses against human α-L-iduronidase when used to treat mucopolysaccharidosis type I.

Authors:  Priscila Keiko Matsumoto Martin; Roberta Sessa Stilhano; Vivian Yochiko Samoto; Christina Maeda Takiya; Giovani Bravin Peres; Yara Maria Correa da Silva Michelacci; Flavia Helena da Silva; Vanessa Gonçalves Pereira; Vânia D'Almeida; Fabio Luiz Navarro Marques; Andreia Hanada Otake; Roger Chammas; Sang Won Han
Journal:  PLoS One       Date:  2014-03-18       Impact factor: 3.240

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.