Human platelet lysates for human cell propagation

被引:102
作者
Barro, Lassina [1 ]
Burnouf, Pierre-Alain [2 ]
Chou, Ming-Li [3 ,4 ]
Nebie, Ouada [3 ]
Wu, Yu-Wen [3 ]
Chen, Ming-Sheng [3 ]
Radosevic, Miryana [2 ]
Knutson, Folke [5 ]
Burnouf, Thierry [1 ,3 ,6 ]
机构
[1] Taipei Med Univ, Coll Biomed Engn, Int PhD Program Biomed Engn, Taipei, Taiwan
[2] Human Prot Proc Sci, Technol Intelligence Dept, Lille, France
[3] Taipei Med Univ, Coll Biomed Engn, Grad Inst Biomed Mat & Tissue Engn, Taipei 11031, Taiwan
[4] St Antoine Hosp, INSERM, CdR St Antoine,UMRS 938, Lab Immune Syst Neuroinflammat & Neurodegenerat D, Paris, France
[5] Uppsala Univ, Clin Immunol & Transfus Med IGP, Uppsala, Sweden
[6] Taipei Med Univ, Coll Med, Int PhD Program Cell Therapy & Regenerat Med, Taipei, Taiwan
关键词
Cell propagation; cell therapy; HPL; human platelet lysate; regenerative medicine;
D O I
10.1080/09537104.2020.1849602
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A pathogen-free and standardized xeno-free supplement of growth media is required for the ex vivo propagation of human cells used as advanced therapeutic medicinal products and for clinical translation in regenerative medicine and cell therapies. Human platelet lysate (HPL) made from therapeutic-grade platelet concentrate (PC) is increasingly regarded as being an efficient xeno-free alternative growth medium supplement to fetal bovine serum (FBS) for clinical-grade isolation and/or propagation of human cells. Most experimental studies establishing the superiority of HPL over FBS were conducted using mesenchymal stromal cells (MSCs) from bone marrow or adipose tissues. Data almost unanimously concur that MSCs expanded in a media supplemented with HPL have improved proliferation, shorter doubling times, and preserved clonogenicity, immunophenotype, in vitro trilineage differentiation capacity, and T-cell immunosuppressive activity. HPL can also be substituted for FBS when propagating MSCs from various other tissue sources, including Wharton jelly, the umbilical cord, amniotic fluid, dental pulp, periodontal ligaments, and apical papillae. Interestingly, HPL xeno-free supplementation is also proving successful for expanding human-differentiated cells, including chondrocytes, corneal endothelium and corneal epithelium cells, and tenocytes, for transplantation and tissue-engineering applications. In addition, the most recent developments suggest the possibility of successfully expanding immune cells such as macrophages, dendritic cells, and chimeric antigen receptor-T cells in HPL, further broadening its use as a growth medium supplement. Therefore, strong scientific rationale supports the use of HPL as a universal growth medium supplement for isolating and propagating therapeutic human cells for transplantation and tissue engineering. Efforts are underway to ensure optimal standardization and pathogen safety of HPL to secure its reliability for clinical-grade cell-therapy and regenerative medicine products and tissue engineering.
引用
收藏
页码:153 / 162
页数:10
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