Literature DB >> 25716730

Analysis of results of acute graft-versus-host disease prophylaxis with donor multipotent mesenchymal stromal cells in patients with hemoblastoses after allogeneic bone marrow transplantation.

I N Shipounova1, N A Petinati, A E Bigildeev, E A Zezina, N I Drize, L A Kuzmina, E N Parovichnikova, V G Savchenko.   

Abstract

Allogeneic bone marrow transplantation (allo-BMT) is currently the only way to cure many hematoproliferative disorders. However, allo-BMT use is limited by severe complications, the foremost being graft-versus-host disease (GVHD). Due to the lack of efficiency of the existing methods of GVHD prophylaxis, new methods are being actively explored, including the use of donors' multipotent mesenchymal stromal cells (MMSC). In this work, we analyzed the results of acute GVHD (aGVHD) prophylaxis by means of MMSC injections after allo-BMT in patients with hematological malignancies. The study included 77 patients. They were randomized into two groups - those receiving standard prophylaxis of aGVHD and those who were additionally infused with MMSC derived from the bone marrow of hematopoietic stem cell donors. We found that the infusion of MMSC halves the incidence of aGVHD and increases the overall survival of patients. Four of 39 MMSC samples were ineffective for preventing aGVHD. Analysis of individual donor characteristics (gender, age, body mass index) and the MMSC properties of these donors (growth parameters, level of expression of 30 genes involved in proliferation, differentiation, and immunomodulation) revealed no significant difference between the MMSC that were effective or ineffective for preventing aGVHD. We used multiple logistic regression to establish a combination of features that characterize the most suitable MMSC samples for the prevention of aGVHD. A model predicting MMSC sample success for aGVHD prophylaxis was constructed. Significant model parameters were increased relative expression of the FGFR1 gene in combination with reduced expression levels of the PPARG and IGF1 genes. Depending on the chosen margin for probability of successful application of MMSC, this model correctly predicts the outcome of the use of MMSC in 82-94% of cases. The proposed model of prospective evaluation of the effectiveness of MMSC samples will enable prevention of the development of aGVHD in the maximal number of patients.

Entities:  

Mesh:

Year:  2014        PMID: 25716730     DOI: 10.1134/S0006297914120104

Source DB:  PubMed          Journal:  Biochemistry (Mosc)        ISSN: 0006-2979            Impact factor:   2.487


  10 in total

1.  Long-term survival of donor bone marrow multipotent mesenchymal stromal cells implanted into the periosteum of patients with allogeneic graft failure.

Authors:  L A Kuzmina; N A Petinati; N V Sats; N J Drize; N V Risinskaya; A B Sudarikov; V A Vasilieva; M Y Drokov; E D Michalzova; E N Parovichnikova; V G Savchenko
Journal:  Int J Hematol       Date:  2016-05-12       Impact factor: 2.490

2.  The Use of Human Mesenchymal Stem Cells as Therapeutic Agents for the in vivo Treatment of Immune-Related Diseases: A Systematic Review.

Authors:  Alessander Leyendecker; Carla Cristina Gomes Pinheiro; Mariane Tami Amano; Daniela Franco Bueno
Journal:  Front Immunol       Date:  2018-09-11       Impact factor: 7.561

3.  Mesenchymal stromal cells as treatment or prophylaxis for acute or chronic graft-versus-host disease in haematopoietic stem cell transplant (HSCT) recipients with a haematological condition.

Authors:  Sheila A Fisher; Antony Cutler; Carolyn Doree; Susan J Brunskill; Simon J Stanworth; Cristina Navarrete; John Girdlestone
Journal:  Cochrane Database Syst Rev       Date:  2019-01-30

4.  Hematopoietic stem cells as a tool for the treatment of glioblastoma multiforme.

Authors:  Igor S Bryukhovetskiy; Inessa V Dyuizen; Valeriy E Shevchenko; Andrey S Bryukhovetskiy; Polina V Mischenko; Elena V Milkina; Yuri S Khotimchenko
Journal:  Mol Med Rep       Date:  2016-10-13       Impact factor: 2.952

Review 5.  The role of mesenchymal stem cells in hematopoietic stem cell transplantation: prevention and treatment of graft-versus-host disease.

Authors:  Lu Zhao; Shanquan Chen; Panxin Yang; Hongcui Cao; Lanjuan Li
Journal:  Stem Cell Res Ther       Date:  2019-06-21       Impact factor: 6.832

6.  Mesenchymal stromal cells for the prophylaxis and treatment of graft-versus-host disease-a meta-analysis.

Authors:  Cynthia Morata-Tarifa; María Del Mar Macías-Sánchez; Antonio Gutiérrez-Pizarraya; Rosario Sanchez-Pernaute
Journal:  Stem Cell Res Ther       Date:  2020-02-18       Impact factor: 6.832

Review 7.  The Effects of Hypoxia on the Immune-Modulatory Properties of Bone Marrow-Derived Mesenchymal Stromal Cells.

Authors:  Zsolt Fábián
Journal:  Stem Cells Int       Date:  2019-10-08       Impact factor: 5.443

8.  Cell therapy with intravascular administration of mesenchymal stromal cells continues to appear safe: An updated systematic review and meta-analysis.

Authors:  Mary Thompson; Shirley H J Mei; Dianna Wolfe; Josée Champagne; Dean Fergusson; Duncan J Stewart; Katrina J Sullivan; Emily Doxtator; Manoj Lalu; Shane W English; John Granton; Brian Hutton; John Marshall; Alies Maybee; Keith R Walley; Claudia Dos Santos; Brent Winston; Lauralyn McIntyre
Journal:  EClinicalMedicine       Date:  2020-01-17

Review 9.  Current status of clinical trials assessing mesenchymal stem cell therapy for graft versus host disease: a systematic review.

Authors:  Ying Li; Jie Hao; Zheng Hu; Yong-Guang Yang; Qi Zhou; Liguang Sun; Jun Wu
Journal:  Stem Cell Res Ther       Date:  2022-03-04       Impact factor: 6.832

10.  Recovery of Donor Hematopoiesis after Graft Failure and Second Hematopoietic Stem Cell Transplantation with Intraosseous Administration of Mesenchymal Stromal Cells.

Authors:  Nataliya Petinati; Nina Drize; Natalia Sats; Natalya Risinskaya; Andrey Sudarikov; Michail Drokov; Daria Dubniak; Alina Kraizman; Maria Nareyko; Natalia Popova; Maya Firsova; Larisa Kuzmina; Elena Parovichnikova; Valeriy Savchenko
Journal:  Stem Cells Int       Date:  2018-04-10       Impact factor: 5.443

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.