Table 4.
The current hurdles in AC repair.
| Treatment strategy | Hurdles |
|---|---|
| Palliative management | 1. Short-term curative effect, long-term drug damage other organs |
| 2. Monosymptomatic resolution, often needs a combined drugs | |
| 3. No effect on injury development and fails to regenerate new AC tissue | |
| 4. Cannot solve the larger damage | |
| Surgical intervention | 1. Robbing Peter to pay Paul |
| 2. Short-term symptom relief and poor prognosis | |
| 3. Complications | |
| 4. Insufficient donors | |
| 5. Incomplete chondrogenesis or rapid degradation and fibrosis of the repaired tissue | |
| 6. The transplant tissue is difficult to preserve and integrate with the surrounding cartilage tissue | |
| 7. Risk of disease transmission | |
| 8. Long recovery time | |
| 9. High costs | |
| 10. Ineffective in repairing large cartilage defects | |
| Gene regulation/ therapy | 1. Requires the effective, safe and durable gene delivery vectors and supportive gene-activated matrices |
| 2. Short duration | |
| 3. Low stability resulting difficult to store and transport | |
| 4. Potential immunogenicity | |
| Stem cell therapy | 1. The stricter regulations on policy and ethics |
| 2. A long culture time and a complex culturing procedure | |
| 3. Cell viability and differentiation capacity were greatly affected by age | |
| 4. Poor cell adhesion and retention | |
| 5. Phenotypic alteration | |
| 6. Heterogeneity | |
| 7. Allograft rejection | |
| 8. High costs | |
| 9. Potential tumorigenicity and immunogenicity | |
| Materials scaffolds | 1. Might intercept cell-cell signaling and exogenous stimulus signals |
| 2. The degradation rate does not match the regeneration rate | |
| 3. Difficult to fully mimic the natural microenvironment resulting poor integration with surrounding cartilage tissue | |
| 4. Complicated preparation process | |
| 5. Solid material leads to inconvenient surgical implantation |