Table 4.
Approach | Advantages | Disadvantages | References |
---|---|---|---|
Intraperitoneal injection of MC‐SeC | Independent from DMD gene mutation | Need for xenogeneic source of SeC | 94, 95 |
All muscles interested thanks to the systemic release of SeC‐derived factors | Caution for PERV presence in pig‐derived SeC, especially in immunosuppressed patients | [108, 109, 110, 111, 112, 113] | |
Combinatorial approach (ie, anti‐inflammatory effect, induction of utrophin expression and release of trophic factors) | ‐ | 94, 95 | |
No need for immunosuppression | ‐ | 15, 18, 19, 20, 21, 22, 94, 95, 106 | |
Single ip injection not requiring incision of the abdominal wall | ‐ | 15, 18, 19, 20, 21, 22, 94, 95, 106 | |
No undesired effects reported in several pre‐clinical settings (including non‐human primates) | ‐ | [15, 18, 19, 20, 21, 22, 94, 95, 102] | |
SeC (non‐encapsulated) already used in clinical trials; no undesired effects reported | ‐ | [106, 107] | |
Alginate‐based microcapsules (containing cells other than SeC) already used in clinical trials; no undesired effects reported | [99, 100, 101] |
MC‐SeC, microencapsulated Sertoli cells; PERVs, porcine endogenous retroviruses; SeC, Sertoli cells.