Literature DB >> 31935514

A significant decrease of BAFF, APRIL, and BAFF receptors following mesenchymal stem cell transplantation in patients with refractory rheumatoid arthritis.

Arezoo Gowhari Shabgah1, Zhaleh Shariati-Sarabi2, Jalil Tavakkol-Afshari1, Ali Ghasemi3, Mohsen Ghoryani4, Mojgan Mohammadi5.   

Abstract

In the present study, we aimed to evaluate effects of autologous mesenchymal stem cells (MSCs) intravenous administration on the response of B cells, BAFF, APRIL, and their receptors on the surface of B cells at 1, 6, and 12 month follow-up periods in refractory rheumatoid arthritis (RA) patients. Thirteen patients with refractory RA received autologous MSCs. Plasma levels of BAFF and APRIL were measured employing ELISA method, followed by estimating B cell population and BAFFRs evaluation by flow cytometry technique. Gene expression of BAFF, APRIL, and their receptors on B cell surface in PBMCs was evaluated by SYBR Green real-time PCR technique. Plasma concentration of BAFF significantly decreased 1 and 6 months after the MSCT (MSCs Transplantation). Plasma concentration of APRIL significantly decreased 1 month after the MSCT. Percentages of CD19 + B cells in the PBMC population significantly decreased 12 months after the MSCT. Percentages of BR3 + CD19 + B cells and BCMA + CD19 + B cells significantly decreased at the 12th month after the MSCT. The gene expression of BAFF in the PBMC population significantly decreased during 6, and 12 months after the MSCT. The gene expression of APRIL significantly decreased on month 6 after the MSCT. The gene expression of BR3 significantly decreased during 1, 6, and 12 months after the MSCT. The MSCT seems to decrease B cells response because of the reduced production of BAFF and APRIL cytokines and decrease the expression of their receptors on the surface of B cells.
Copyright © 2020 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  APRIL protein; B-lymphocytes; BAFF ligand; BAFF receptors; Mesenchymalstem cell transplantation; Rheumatoid arthritis

Mesh:

Substances:

Year:  2020        PMID: 31935514     DOI: 10.1016/j.gene.2020.144336

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  16 in total

1.  Synergistic effect of Bruton's tyrosine kinase and TNF-α in the regulation of rheumatoid arthritis and underlying mechanisms.

Authors:  Jinwan Du
Journal:  Exp Ther Med       Date:  2021-12-14       Impact factor: 2.447

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Authors:  Jehan J El-Jawhari; Yasser El-Sherbiny; Dennis McGonagle; Elena Jones
Journal:  Front Immunol       Date:  2021-02-24       Impact factor: 7.561

3.  Intravenous injection of autologous bone marrow-derived mesenchymal stem cells on the gene expression and plasma level of CCL5 in refractory rheumatoid arthritis.

Authors:  Mina Alavi; Jalil Tavakkol-Afshari; Zhaleh Shariati-Sarabi; Arezoo Gowhari Shabgah; Mohsen Ghoryani; Ali Ghasemi; Mojgan Mohammadi
Journal:  J Res Med Sci       Date:  2020-12-30       Impact factor: 1.852

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Journal:  Front Immunol       Date:  2021-09-28       Impact factor: 7.561

Review 7.  The Immunomodulatory Effects of Mesenchymal Stem Cells on Regulatory B Cells.

Authors:  Jialing Liu; Qiuli Liu; Xiaoyong Chen
Journal:  Front Immunol       Date:  2020-08-14       Impact factor: 7.561

Review 8.  Mesenchymal Stem/Stromal Cells for Rheumatoid Arthritis Treatment: An Update on Clinical Applications.

Authors:  Mercedes Lopez-Santalla; Raquel Fernandez-Perez; Marina I Garin
Journal:  Cells       Date:  2020-08-07       Impact factor: 6.600

Review 9.  Immunomodulatory Effects of Mesenchymal Stem Cells and Mesenchymal Stem Cell-Derived Extracellular Vesicles in Rheumatoid Arthritis.

Authors:  Huan Liu; Ruicen Li; Tao Liu; Leiyi Yang; Geng Yin; Qibing Xie
Journal:  Front Immunol       Date:  2020-08-20       Impact factor: 7.561

Review 10.  Rheumatoid Arthritis: Pathogenic Roles of Diverse Immune Cells.

Authors:  Sunhee Jang; Eui-Jong Kwon; Jennifer Jooha Lee
Journal:  Int J Mol Sci       Date:  2022-01-14       Impact factor: 5.923

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