Van T Hoang1, Quynh-Mai Trinh2, Dam Thi Minh Phuong3, Hue Thi Hong Bui3, Le Minh Hang3, Nguyen Thi Hong Ngan3, Nguyen Thi Tuyet Anh3, Phung Yen Nhi2, Trinh Thi Hong Nhung3, Ha Thi Lien4, Tu Dac Nguyen4, Liem Nguyen Thanh5, Duc M Hoang2. 1. Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam. Electronic address: v.vanht8@vinmec.com. 2. Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam. 3. Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam; College of Health Science, VinUniversity, Hanoi, Vietnam. 4. College of Health Science, VinUniversity, Hanoi, Vietnam. 5. Vinmec Research Institute of Stem Cell and Gene Technology, Vinmec Healthcare System, Hanoi, Vietnam; Vinmec HiTech Center, Vinmec Healthcare System, Hanoi, Vietnam.
Abstract
BACKGROUND AIMS: Mesenchymal stem/stromal cells (MSCs) are of interest for the treatment of graft-versus-host disease, autoimmune diseases, osteoarthritis and neurological and cardiovascular diseases. Increasing numbers of clinical trials emphasize the need for standardized manufacturing of these cells. However, many challenges related to diverse isolation and expansion protocols and differences in cell tissue sources exist. As a result, the cell products used in numerous trials vary greatly in characteristics and potency. METHODS: The authors have established a standardized culture platform using xeno- and serum-free commercial media for expansion of MSCs derived from umbilical cord (UC), bone marrow and adipose-derived (AD) and examined their functional characteristics. RESULTS: MSCs from the tested sources stably expanded in vitro and retained their biomarker expression and normal karyotype at early and later passages and after cryopreservation. MSCs were capable of colony formation and successfully differentiated into osteogenic, adipogenic and chondrogenic lineages. Pilot expansion of UC-MSCs and AD-MSCs to clinical scale revealed that the cells met the required quality standard for therapeutic applications. CONCLUSIONS: The authors' data suggest that xeno- and serum-free culture conditions are suitable for large-scale expansion and enable comparative study of MSCs of different origins. This is of importance for therapeutic purposes, especially because of the numerous variations in pre-clinical and clinical protocols for MSC-based products.
BACKGROUND AIMS: Mesenchymal stem/stromal cells (MSCs) are of interest for the treatment of graft-versus-host disease, autoimmune diseases, osteoarthritis and neurological and cardiovascular diseases. Increasing numbers of clinical trials emphasize the need for standardized manufacturing of these cells. However, many challenges related to diverse isolation and expansion protocols and differences in cell tissue sources exist. As a result, the cell products used in numerous trials vary greatly in characteristics and potency. METHODS: The authors have established a standardized culture platform using xeno- and serum-free commercial media for expansion of MSCs derived from umbilical cord (UC), bone marrow and adipose-derived (AD) and examined their functional characteristics. RESULTS: MSCs from the tested sources stably expanded in vitro and retained their biomarker expression and normal karyotype at early and later passages and after cryopreservation. MSCs were capable of colony formation and successfully differentiated into osteogenic, adipogenic and chondrogenic lineages. Pilot expansion of UC-MSCs and AD-MSCs to clinical scale revealed that the cells met the required quality standard for therapeutic applications. CONCLUSIONS: The authors' data suggest that xeno- and serum-free culture conditions are suitable for large-scale expansion and enable comparative study of MSCs of different origins. This is of importance for therapeutic purposes, especially because of the numerous variations in pre-clinical and clinical protocols for MSC-based products.
Authors: Duc M Hoang; Phuong T Pham; Trung Q Bach; Anh T L Ngo; Quyen T Nguyen; Trang T K Phan; Giang H Nguyen; Phuong T T Le; Van T Hoang; Nicholas R Forsyth; Michael Heke; Liem Thanh Nguyen Journal: Signal Transduct Target Ther Date: 2022-08-06
Authors: Maria Eugenia Fernández-Santos; Mariano Garcia-Arranz; Enrique J Andreu; Ana Maria García-Hernández; Miriam López-Parra; Eva Villarón; Pilar Sepúlveda; Francisco Fernández-Avilés; Damian García-Olmo; Felipe Prosper; Fermin Sánchez-Guijo; Jose M Moraleda; Agustin G Zapata Journal: Front Immunol Date: 2022-06-09 Impact factor: 8.786
Authors: Liem Nguyen Thanh; Van T Hoang; Huong Le Thu; Phuong Anh Thi Nguyen; Duc M Hoang; Doan Van Ngo; Hung Cao Vu; Van Nguyen Thi Bich; Michael Heke Journal: Cell Transplant Date: 2022 Jan-Dec Impact factor: 4.139
Authors: Minh Quang Nguyen; Hue T H Bui; Anh Nguyen Thi Tuyet; Trinh Thi Hong Nhung; Duc M Hoang; Nguyen Thanh Liem; Van T Hoang Journal: Cell Transplant Date: 2021 Jan-Dec Impact factor: 4.064
Authors: Liem Thanh Nguyen; Nghia Trung Tran; Uyen Thi Trang Than; Minh Quang Nguyen; Anh Minh Tran; Phuong Thi Xuan Do; Thao Thi Chu; Tu Dac Nguyen; Anh Viet Bui; Tien Anh Ngo; Van Thanh Hoang; Nhung Thi My Hoang Journal: Stem Cell Res Ther Date: 2022-01-10 Impact factor: 6.832
Authors: Anh T L Ngo; Hang M Le; Nhung T H Trinh; Adriel Peng Guo Jun; Trung Q Bach; Hue T H Bui; Van T Hoang; Anh V Bui; Liem T Nguyen; Duc M Hoang Journal: J Cell Mol Med Date: 2021-10-27 Impact factor: 5.310
Authors: Van T Hoang; Hoang-Phuong Nguyen; Viet Nhan Nguyen; Duc M Hoang; Tan-Sinh Thi Nguyen; Liem Nguyen Thanh Journal: Front Cell Dev Biol Date: 2022-09-28