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Showing papers on "Mesoangioblast published in 2021"


Journal ArticleDOI
TL;DR: In this paper, the authors provide an overview on stem cell lineages employed for strategies in muscular dystrophies (MDs), with a focus on adult stem cells and progenitor cells resident in skeletal muscle.
Abstract: The intrinsic regenerative capacity of skeletal muscle makes it an excellent target for cell therapy. However, the potential of muscle tissue to renew is typically exhausted and insufficient in muscular dystrophies (MDs), a large group of heterogeneous genetic disorders showing progressive loss of skeletal muscle fibers. Cell therapy for MDs has to rely on suppletion with donor cells with high myogenic regenerative capacity. Here, we provide an overview on stem cell lineages employed for strategies in MDs, with a focus on adult stem cells and progenitor cells resident in skeletal muscle. In the early days, the potential of myoblasts and satellite cells was explored, but after disappointing clinical results the field moved to other muscle progenitor cells, each with its own advantages and disadvantages. Most recently, mesoangioblasts and pericytes have been pursued for muscle cell therapy, leading to a handful of preclinical studies and a clinical trial. The current status of (pre)clinical work for the most common forms of MD illustrates the existing challenges and bottlenecks. Besides the intrinsic properties of transplantable cells, we discuss issues relating to cell expansion and cell viability after transplantation, optimal dosage, and route and timing of administration. Since MDs are genetic conditions, autologous cell therapy and gene therapy will need to go hand-in-hand, bringing in additional complications. Finally, we discuss determinants for optimization of future clinical trials for muscle cell therapy. Joined research efforts bring hope that effective therapies for MDs are on the horizon to fulfil the unmet clinical need in patients.

8 citations


Book ChapterDOI
TL;DR: An overview of the current techniques for isolation and characterization of rodent, canine, human, and equine adult mesoangioblasts can be found in this paper, where a phase I-II clinical trial showed that intra-arterial HLA-matched MABs were relatively safe.
Abstract: Mesoangioblasts (MABs) are vessel-associated stem cells that express pericyte markers and are originally isolated from the embryonic dorsal aorta From postnatal small vessels of skeletal muscle and heart, it is possible to isolate cells with similar characteristics to embryonic MABs Adult MABs have the capacity to self-renew and to differentiate into cell types of mesodermal lineages upon proper culture conditions To date, the origin of MABs and the relationship with other muscle stem cells are still debated Recently, in a phase I-II clinical trial, intra-arterial HLA-matched MABs were proved to be relatively safe Novel information on MAB pure populations is desirable, and implementation of their therapeutic potential is mandatory to approach efficacy in MAB-based treatments This chapter provides an overview of the current techniques for isolation and characterization of rodent, canine, human, and equine adult MABs

3 citations