Mesenchymal Stem Cell Benefits Observed in Bone Marrow Failure and Acquired Aplastic Anemia

Author:

Gonzaga Vivian Fonseca123,Wenceslau Cristiane Valverde3ORCID,Lisboa Gustavo Sabino13,Frare Eduardo Osório1,Kerkis Irina1ORCID

Affiliation:

1. Laboratory of Genetics, Butantan Institute, São Paulo, SP, Brazil

2. Post-Graduate Program Interunity in Biotechnology, University of São Paulo, São Paulo, SP, Brazil

3. CellAvita Ltd, Valinhos, SP, Brazil

Abstract

Acquired aplastic anemia (AA) is a type of bone marrow failure (BMF) syndrome characterized by partial or total bone marrow (BM) destruction resulting in peripheral blood (PB) pancytopenia, which is the reduction in the number of red blood cells (RBC) and white blood cells (WBC), as well as platelets (PLT). The first-line treatment option of AA is given by hematopoietic stem cell (HSCs) transplant and/or immunosuppressive (IS) drug administration. Some patients did not respond to the treatment and remain pancytopenic following IS drugs. The studies are in progress to test the efficacy of adoptive cellular therapies as mesenchymal stem cells (MSCs), which confer low immunogenicity and are reliable allogeneic transplants in refractory severe aplastic anemia (SAA) cases. Moreover, bone marrow stromal cells (BMSC) constitute an essential component of the hematopoietic niche, responsible for stimulating and enhancing the proliferation of HSCs by secreting regulatory molecules and cytokines, providing stimulus to natural BM microenvironment for hematopoiesis. This review summarizes scientific evidences of the hematopoiesis improvements after MSC transplant, observed in acquired AA/BMF animal models as well as in patients with acquired AA. Additionally, we discuss the direct and indirect contribution of MSCs to the pathogenesis of acquired AA.

Publisher

Hindawi Limited

Subject

Cell Biology,Molecular Biology

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