TY - JOUR
T1 - Advances in mesenchymal stem cell therapy for immune and inflammatory diseases
T2 - Use of cell-free products and human pluripotent stem cell-derived mesenchymal stem cells
AU - Wang, Li Tzu
AU - Liu, Ko Jiunn
AU - Sytwu, Huey Kang
AU - Yen, Men Luh
AU - Yen, B. Linju
N1 - Funding Information:
This work was partially funded by the Ministry of Science Technology, Taiwan (MOST109‐2326‐B‐002 ‐016‐MY3 to L.T.W. and MOST107‐2314‐B‐002‐104‐MY3 to M.L.Y.) and the NHRI (10A1‐CSPP06 and CS‐110‐GP01 to B.L.Y.).
Publisher Copyright:
© 2021 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals LLC on behalf of AlphaMed Press.
PY - 2021/9
Y1 - 2021/9
N2 - Mesenchymal stem cell therapy (MSCT) for immune and inflammatory diseases continues to be popular based on progressive accumulation of preclinical mechanistic evidence. This has led to further expansion in clinical indications from graft rejection, autoimmune diseases, and osteoarthritis, to inflammatory liver and pulmonary diseases including COVID-19. A clear trend is the shift from using autologous to allogeneic MSCs, which can be immediately available as off-the-shelf products. In addition, new products such as cell-free exosomes and human pluripotent stem cell (hPSC)-derived MSCs are exciting developments to further prevalent use. Increasing numbers of trials have now published results in which safety of MSCT has been largely demonstrated. While reports of therapeutic endpoints are still emerging, efficacy can be seen for specific indications—including graft-vs-host-disease, strongly Th17-mediated autoimmune diseases, and osteoarthritis—which are more robustly supported by mechanistic preclinical evidence. In this review, we update and discuss outcomes in current MSCT clinical trials for immune and inflammatory disease, as well as new innovation and emerging trends in the field.
AB - Mesenchymal stem cell therapy (MSCT) for immune and inflammatory diseases continues to be popular based on progressive accumulation of preclinical mechanistic evidence. This has led to further expansion in clinical indications from graft rejection, autoimmune diseases, and osteoarthritis, to inflammatory liver and pulmonary diseases including COVID-19. A clear trend is the shift from using autologous to allogeneic MSCs, which can be immediately available as off-the-shelf products. In addition, new products such as cell-free exosomes and human pluripotent stem cell (hPSC)-derived MSCs are exciting developments to further prevalent use. Increasing numbers of trials have now published results in which safety of MSCT has been largely demonstrated. While reports of therapeutic endpoints are still emerging, efficacy can be seen for specific indications—including graft-vs-host-disease, strongly Th17-mediated autoimmune diseases, and osteoarthritis—which are more robustly supported by mechanistic preclinical evidence. In this review, we update and discuss outcomes in current MSCT clinical trials for immune and inflammatory disease, as well as new innovation and emerging trends in the field.
KW - autoimmune diseases
KW - clinical trials
KW - exosomes
KW - extracellular vesicles
KW - graft rejection
KW - human
KW - human pluripotent stem cells
KW - liver cirrhosis
KW - mesenchymal stem/stromal cell therapy
KW - organ transplantation
KW - pulmonary inflammation
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U2 - 10.1002/sctm.21-0021
DO - 10.1002/sctm.21-0021
M3 - Review article
C2 - 34008922
AN - SCOPUS:85106320771
SN - 2157-6564
VL - 10
SP - 1288
EP - 1303
JO - Stem cells translational medicine
JF - Stem cells translational medicine
IS - 9
ER -