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. 2022 Jul 11;11(14):2165. doi: 10.3390/cells11142165

Table 2.

Stem-cell therapies in NMOSD.

Applied Cells First Author Reference Patients (n) AQ4 IgG-Positive Age Females (n) EDSS (before Treatment) Follow-Up Duration (Months) Outcome (Beneficial Effects) *****, %
HSC (auto) Burton 79 3 2 34 ** 2 4 * 108 67
Khan 85 1 1 2 1 ND 6 0
Carlisle 80 1 1 40 1 ND 24 100
Burt 78 13 12 42 ** 11 4.3 ** 57 80 ****
Aouad 82 1 1 47 1 6.5 12 100
Greco 77 16 10 37 * 13 6.5 * 47 88
Hoay 81 3 ND 31.7 ** 1 3.5 * 88 100
Matiello 83 1 1 64 1 ND 24 0
Peng 84 1 ND 23 1 5 6 100
HSC (allo) Hau 88 1 1 15 0 8.5 48 100
Ceglie 86 1 1 9 1 6.5 24 100
Greco 87 2 1 29 ** 1 7.5 * 42 100
MSC (auto) Fu 91 15 13 47 ** 14 4.9 ** 24 100
MSC (allo) Lu 89 5 5 25.4 ** 5 5 * 70 60
Lu 90 5 5 35 ** 5 5.1 ** 24 80
Peptide-loaded tolerogenic
dendritic cells
Zubizarreta 9 4 4 40 ** 3 4.8 ** 3 100

NMOSD = neuromyelitis optica spectrum disorders; AQP4 IgG = aquaporin-4 immunoglobulin G antibody; EDSS = expanded disability status scale; HSC = hematopoietic stem cell; MSC = mesenchymal stem cell; auto = autologous; allo = allogeneic; * = median; ** = mean; **** considering 12 patients (excluding one patient with NMOSD and concomitant systemic lupus erythematosus); ***** = improvement or stability of EDSS scores during follow-up; ND = no data.