Copyright
©The Author(s) 2020.
World J Transplant. Nov 28, 2020; 10(11): 330-344
Published online Nov 28, 2020. doi: 10.5500/wjt.v10.i11.330
Published online Nov 28, 2020. doi: 10.5500/wjt.v10.i11.330
Treatment target | Trial phase | Source of EVs | EV manipulation | Results |
Pancreatic cancer (NCT03608631) | Phase I | MSC, allogeneic | siRNA direct loading | Not yet recruiting |
Colon cancer[72] | Phase I | Plant origin | Curcumin direct loading | Active |
Melanoma[73] | Phase I | Immature DCs, autologous | Tumor antigen (peptide) direct loading | Safe, well tolerated, mixed responses. |
Non-small cell lung cancer (NCT01159288) | Phase II | Mature DCs, autologous | Tumor antigen (peptide) direct loading | Safe, well tolerated, mixed responses. |
Non-small cell lung cancer[74] | Phase I | Immature DCs, autologous | Tumor antigen (peptide) direct loading | Safe, well tolerated, mixed responses. |
Malignant ascites (NCT01854866) | Phase II | Tumor derived | Chemotherapeutic agent loading | Unknown |
Acute ischaemic stroke (NCT03384433) | Phase I/II | MSCs, allogeneic | miRNA loading | Completed |
- Citation: Mastoridis S, Martinez-Llordella M, Sanchez-Fueyo A. Extracellular vesicles as mediators of alloimmunity and their therapeutic potential in liver transplantation. World J Transplant 2020; 10(11): 330-344
- URL: https://www.wjgnet.com/2220-3230/full/v10/i11/330.htm
- DOI: https://dx.doi.org/10.5500/wjt.v10.i11.330