MSC source | Type of cases | Administration route | Main findings | ref |
---|---|---|---|---|
MSC-derived exosomes | Mouse model | Topical application | Concentration of key mediators, such as IL-17 and IL-23 (↓) Formation of NETs by C5b-9 formation (↓) Function of neutrophils (↓) | [54] |
MSC-derived exosomes | Mouse model | Intraperitoneal injection and Topical application | Formation of C5-9 And NETs (↓) Production of IL-17 by neutrophils (↓) | [55] |
hUC-MSC | Mouse model | Tail vein Injection | Number of CD11b + Ly6G + neutrophils (↓) Formation of NETs (↓) Expression of neutrophilic enzymes (like MPO and CRAMP) Level of keratin 16 (K16) (↓) Level of S100A7, S100A8, and S100A9 (↓) Levels of pro-inflammatory factors (↓) Expression of IL-10 (↑) and IL-17 (↓) Number of Th2 (↑) | [56] |
hUC-MSC pretreated with IFN-γ and TNF-α | Mouse model | Subcutaneous Injection | Improvement in clinical symptoms, and spleen evaluation decreased the relative expression of CXCL1 (neutrophils migration (↓)) and inhibited STAT1 phosphorylation in keratinocytes (Healing of psoriatic lesions (↑)) | [58] |
hUC-MSCs | Mouse model | Tail vein Injection | TNF-α concentration in culture medium (↓) Matrix metalloproteinase (MMP)-13 (↓) | [64] |
hUC-MSCs | Mouse model and cell culture | Subcutaneous injection | Level of pro-inflammatory cytokines (↓) Expression of IL-10 and IDO in DCs (↑) Differentiation of Th0 into Th1, Th2, and Th17 cells (↓) Migration and implantation of CD11c+, CD11b+, and CD4 + cells (↓) Treg differentiation (↑) | [69] |
T-MSC | Mouse model | Tail vein Injection | Th17 differentiation (via PD-1/PD-L1 interaction) (↓) Volume, mass, and number of splenocytes (↓) PASI score (↓) Expression of IL-17, IL-22, IL-23, TNF-α, IFN-γ, K6, K16, and CCL20 genes (↓) Expression of PD-1 in T lymphocytes (↑) | [72] |
Small EVs derived from IFN-γ-activated hUCB-MSCs | Mouse model and cell culture | Intradermal injection | Th17 exhaustion (↑) Th2 differentiation (↑) Inflammatory mediators including IL-17 A, IFN-γ, IL-6, and TNF-α (↓) PASI score (↓) Activity of the miR-210 molecule (plays a role in the differentiation of Th1/Th17) (↓) | [73] |
BM-MSCs and AD-MSCs | Mouse model | Intravenous injection | PASI score (↓) Number of CD3 + cells (↓) Expression of S100A9/7 and CCL17 (↓) | [75] |
hE-MSC | Mouse model | Subcutaneous injection | Th1 and Th17 secretome (such as TNF-α, IFN-γ, IFN-α, IL-27, IL-17 A and IL-23) (↓) Improvement in clinical symptoms (↑) | [76] |
T-MSCs | Mouse model and cell culture | Intravenous injection | Level of osteoprotegerin (OPG) (↑) and (RANK)/RANKL interaction between Th17 and osteoclast (↓) PASI score (↓) | [77] |
MSCs and SOD3-induced MSCs | Mouse model | Subcutaneous injection | Psoriatic epidermal thickness (↓) Mass and number of spleen and lymph nodes cells (↓) Number and proliferation of T lymphocytes, neutrophils, and DC (↓) and number of Treg (↑) Inhibitory molecules such as IL-10, TGF-β, and Foxp3 (↑) Decrease in IL-17, IL-22, IL-6, and IL-23, and transcription factors such as STAT1, STAT3, JAK1, RoR-γt (↓) Activation of NF-κB, MAPK (↓) cAMP and PKA/CREB (↑) and anti-inflammatory phenotype (↑) | [80] |
G-MSC | Mouse model | Tail vein Injection | PASI score (↓) Number of CD3 + CD25 + T lymphocytes (↑) and CD3 + CD17 + T lymphocytes (↓) Concentration of IL-6, IL-17 A, IL-17 F, IL-21, and TNF-α (↓) and concentration of IL-10 | [87] |
hUCB-MSCs | Phase 1/2a (17 patients) | Intravenous injection | Population of CD3 + CD4 + CD25 + CD127-/low Tregs and CD3 + CD8 + CCR7 + CD45RA- memory T cells (↑) PASI, PGA and BSA score (↓) neutrophil count (↓) IgG titer (↓) BUN levels (↓) | [88] |
DPSC and HGF-DPSC | Mouse model and cell culture | ? | Number of Th1 and Th17 cells (↓) and Treg (↑) CK6 and CK17 (↓) pro-inflammatory factors such as IFN-γ, TNF-α, and IL-17 A (↓) IL-10 expression (↑) expression of T-bet, RoR-γt, IL-17 A, IL-17 F, and IL-23 (↓) and FOXP3 (↑) | [89] |
dermal MSCs | Cell culture | - | Expression of the TGF-β receptor (↑) Ratio of Tregs to Th17 cells (↑) | [90] |