Stem cell-derived exosome treatment for acute spinal cord injury: a systematic review and meta-analysis based on preclinical evidence

Background: The study aims were to systematically review and analyze preclinical research on the efficacy of exosomes derived from various mesenchymal stem cell sources (MSC-exos) for the treatment of spinal cord contusion injury (SCI) in small animal models.

Methods: We conducted a systematic search of PubMed, Embase and Google Scholar databases from their inception through February 29, 2024, to identify eligible English-language studies based on predefined inclusion and exclusion criteria. Two independent investigators performed literature screening, data extraction and bias assessment.

Results: A total of 235 rats were used to assess locomotor recovery at the initial assessment, and exhibited significant improvement in hind limb movement in those treated with exosomes, as indicated by a statistically significant increase in Basso-Beattie-Bresnahan (BBB) scores (MD: 1.26, 95% CI: 1.14–1.38, p < 0.01) compared to the controls. This trend persisted in final assessment data across 21 studies, with pooled analysis confirming similar results (MD: 1.56, 95% CI: 1.43–1.68, p < 0.01). Funnel plot analysis indicated asymmetry in the pooled BBB scores at both baseline and endpoint assessments, suggesting potential publication bias. Exosomes were derived from bone marrow, adipose tissue, umbilical cord or human placental MSCs. Meta-analysis results showed no statistically significant differences in therapeutic efficacy among these MSC-exos sources at various treatment time points.

Conclusion: MSC-exos demonstrated considerable promise in improving motor function in SCI-affected rats, with bone marrow MSC-derived exosomes having particularly notable effectiveness.

1 Background

Traumatic spinal cord injury (SCI) is a severe and often life-altering condition, leading to high rates of morbidity and permanent disability worldwide (1). Each year, between 250,000 and 500,000 people experience SCI, primarily due to causes such as vehicle accidents and violence, with over 27 million individuals living with SCI-induced disabilities globally (2). Mechanistically, SCI often results from direct contusion (where external force impacts the spinal cord), hyperextension (overstretching beyond physiological limits), distraction (vertebral separation), or laceration/transection (cutting or severing of the spinal cord) (3, 4). Additionally, secondary injuries from ischemia, inflammation, and excitotoxicity exacerbate motor and sensory deficits, leading to long-term complications (5).

The standard early interventions for acute SCI primarily involve surgical approaches, such as decompression, spinal fixation and fusion, aimed at repairing initial damage and preventing spinal deformities, pain and nerve complications (6). Later-stage treatments include drugs, hyperbaric oxygen therapy and physical interventions to reduce injury progression (7). However, these treatments often fall short in delivering satisfactory outcomes for SCI patients, highlighting an urgent need for alternative therapies (8). Addressing these limitations through innovative approaches such as stem cell exosome therapy may offer improved outcomes, underscoring the necessity of advancing research in this area.

Among emerging therapies, mesenchymal stem cell (MSC)-based treatments are showing promise for SCI management (9). Numerous preclinical studies have demonstrated that stem cells have multifaceted therapeutic properties, including the ability to repair the blood-spinal cord barrier, reduce neuronal apoptosis, promote angiogenesis, regenerate axons and mitigate glial scarring and inflammation (10). Current clinical trials (phase 1 and 2) are exploring the safety and efficacy of MSCs in treating SCI, yet they also reveal adverse effects that necessitate careful consideration (11). Challenges such as low graft survival, immune rejection, genetic variability and potential tumorigenesis continue to impede the broader clinical application of stem cell therapies (12).

Recent research has highlighted the pivotal role of MSC-derived exosomes (MSC-exos) for the effectiveness of stem cell therapies (13). Exosomes – small vesicles with a phospholipid bilayer – transport specific proteins, DNA, mRNA and microRNA from stem cells to target cells, influencing cellular functions and promoting genotypic and phenotypic changes (14, 15). Functionally, exosomes enhance angiogenesis, promote axon regeneration, modulate immune responses, inhibit apoptosis and strengthen the blood-spinal cord barrier, supporting SCI repair (16). Compared to stem cells, exosomes offer advantages such as non-tumorigenicity, structural stability, low immunogenicity and improved capillary permeability, making them promising candidates for preclinical SCI research (17, 18).

Despite the growing interest in stem cell-derived exosomes for SCI therapy, the specific extent of their therapeutic benefits remains insufficiently defined in the current literature (19). The present study aims were to address this critical gap by conducting a systematic review and meta-analysis to evaluate the efficacy and feasibility of MSC-exos for SCI treatment in animal models. By synthesizing available research, this investigation provides valuable evidence to guide future studies and clinical applications, ultimately contributing to improved therapeutic strategies for individuals with SCI.

2 Methods

2.1 Search strategies and protocol

The present meta-analysis focused exclusively on published preclinical investigations involving MSC-exos in rodent models of spinal cord contusion injury. A comprehensive search encompassed only English-language literature across prominent databases such as PubMed, Embase, Web of Science and Google scholar, spanning the period from inception to Feb 29, 2024. The search strategy was crafted to include relevant terms, such as “stem cell-derived exosomes,” “exosomes,” and “spinal cord injury” or “SCI,” within titles and abstracts. A detailed outline of the database search strategy is presented in Figure 1. Furthermore, adherence to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines ensured methodological rigor, with the development of a search strategy aligned with the PICOS (Population, Intervention, Comparison, Outcome, Study design) framework (20). It is worth noting that this systematic review and meta-analysis did not require ethical approval or the consent of individuals to participate.

Figure 1

Figure 1. PRISMA flow chart for the article selection process.

2.2 Inclusion criteria

The criteria for study inclusion were: (i) only studies that utilized rat SCI models induced solely by contusion on a single vertebra were considered, aiming to mitigate heterogeneity arising from variations in animal models and SCI mechanisms, thus aligning with clinical scenarios; (ii) studies that investigated the intravenous transplantation of stem cell-derived exosomes; (iii) studies that compared the therapeutic efficacy of stem cell-derived exosomes with their respective negative controls in the context of SCI treatment being sought; and (iv) studies that provided Basso-Beattie-Bresnahan (BBB) scores for an objective assessment of motor recovery were prioritized (21). These stringent criteria ensured the selection of studies meeting high standards of methodological rigor and relevance to the research objectives.

2.3 Exclusion criteria

Detailed exclusion criteria were: (i) studies that involved exosomes originating from non-MSCs or those without clear exosome origin; (ii) studies that utilized animal models other than rats, such as mice, dogs, monkeys etc.; (iii) studies that employed animal models generated by spinal cord transection or ischemic-perfusion injury; (iv) studies devoid of a control group for comparison; (v) articles lacking reports on BBB scores for assessing functional recovery; (vi) studies that were systematic reviews, meta-analyses, case reports, meeting abstracts, communication letters and similar publications; and (vii) studies published in a journal with an impact factor < 1 (22). These criteria ensured the selection of studies with a high degree of relevance and methodological stringency, which enhanced the robustness of our meta-analysis.

2.4 Data extraction

Two independent investigators conducted a comprehensive review of the selected literature and extracted relevant data from articles meeting the predefined inclusion and exclusion criteria. The extracted data were systematically organized in an Excel spreadsheet, categorized by author, publication year, species, body weight, SCI segment, exosome origin, dosage, administration frequency, mode of administration, potential mechanism and citation details. For data presented in graphical rather than tabular form, the online platform PlotDigitizer was utilized to extract accurately relevant information.

2.5 Study quality assessment

Quality assessment of all included studies was conducted using SYRCLE’s tool, which provides a comprehensive evaluation of bias risk in animal studies. This tool examines ten essential domains: methodological consistency, baseline comparability, allocation concealment, housing standardization, investigator blinding, outcome randomization, assessor blinding, outcome completeness, outcome reporting consistency, and other potential biases. This thorough evaluation ensured adherence to established standards, thereby enhancing the robustness and reliability of our data.

2.6 Data synthesis and statistical analysis

The BBB locomotor rating scale has become a widely used tool for assessing the behavioral impact of SCI in rats, with scores ranging from 0 (no hind limb movement) to 21 (normal locomotion). Its sensitivity allows for precise differentiation of hind limb locomotor abilities across varying injury severities. Consequently, in the selected studies, improvements in locomotor function were measured using the BBB scale, focusing specifically on hind limb motor function (23). This approach ensured standardized and accurate evaluations, enabling a nuanced understanding of therapeutic effects across different SCI severities.

Data from all included studies were synthesized and analyzed using the meta-package in R software (version 4.3.1, University of Auckland, New Zealand). An initial pairwise meta-analysis was conducted to evaluate the effectiveness of MSC-exos in SCI repair, presenting all outcomes as standardized mean differences (SMDs) with 95% confidence intervals (CIs). In cases of significant heterogeneity (p ≤ 0.05 or I² > 50%), a random-effects model was applied; otherwise, a fixed-effects model was used. After addressing major sources of heterogeneity, the random-effects model was consistently applied for further analyses.

Using the “meta” R package, a comprehensive meta-analysis was conducted to evaluate the therapeutic efficacy of exosomes derived from stem cell sources. Fixed-effect models were applied under the assumption of a consistent true effect size across all included animal studies. Given the limited number of trials per comparison and the prevalence of single-trial evaluations, fixed-effect models were appropriate, eliminating the need to estimate between-study heterogeneity and thus enhancing the robustness of our findings.

To evaluate publication bias, funnel plots were created to visually inspect for any missing smaller studies with minimal effect sizes. Assuming no publication bias, a symmetrical distribution of studies around the pooled effect size was expected, represented by a central vertical line on the funnel plot. Asymmetry in the funnel plot indicates potential publication bias, which was quantified using Egger’s test – a statistical measure specifically designed to assess funnel plot asymmetry.

3 Results

3.1 Literature retrieval

A comprehensive keyword search across five databases yielded 276 articles. After removing duplicates, the titles and abstracts of the remaining 217 articles were reviewed, leading to the identification of 45 articles that initially appeared to meet the inclusion criteria. However, upon thorough full-text examination, the selection was refined to 21 articles that clearly met all predefined criteria. The detailed process of literature screening, with each stage of selection, is illustrated in Figure 1.

3.2 Baseline demographics of the included studies

The selection process yielded 21 articles, comprising a study group of 235 rats and a control group of 229 rats. The rats, aged 6 to 24 weeks, weighed between 120 and 350 g. Sample sizes within each experimental group varied from 6 to 25 rats. Across these studies, contusion was the predominant modeling method used. Exosomes derived from bone marrow, adipose tissue, umbilical cord, and human placental MSCs were used in the interventions. Bone marrow MSC-derived exosomes were featured in 12 studies, while exosomes from the other sources appeared in two studies each, except for those sourced from the umbilical cord, which were used in five studies.The therapeutic exosome dosage ranged from 100 to 400 mg, administered uniformly through the tail vein. Notably, exosome administration occurred within 12 h post-model induction. For a detailed summary of each study’s characteristics (24–44), readers are directed to view Table 1 for detailed information.

Table 1

Table 1. Characteristics of the included studies.

The 21 studies on MSC-exos treatment in acute spinal injury revealed a range of intricate and diverse therapeutic mechanisms. These included modulating M2 macrophage polarization within the SCI environment through IRF5 downregulation and promoting axonal regeneration via the PTEN/AKT/mTOR pathway, with further therapeutic benefits from CTGF gene silencing. Notable actions also encompassed neurofilament regeneration, reducing inflammation by modulating the TLR4/NF-κB signaling pathway, and balancing microglial M1/M2 polarization. Additionally, exosomes enhanced TGF-β upregulation, supporting microvascular stability and activated the NGF/TrkA signaling pathway to promote neurotrophic support. Other critical mechanisms included downregulation of phosphorylated NFκB P65 and endothelin-1, which inhibited pericyte pyroptosis, and stimulation of endogenous neurogenesis. Collectively, these findings underscored the robust therapeutic potential and multifaceted modulatory effects of MSC-exos in SCI treatment.

3.3 Comparison of BBB scores between exosome-treated and control rats

A comprehensive analysis of all studies was conducted, involving a total of 235 rats, that reported locomotor recovery outcomes at initial assessment. The findings showed a significant improvement in hind limb movement in exosome-treated rats, as indicated by a statistically significant increase in BBB scores (mean difference: 1.26, 95% CI: 1.14–1.38, p < 0.01) compared to control rats at the first measurement (Figure 2). This trend continued in the final assessments, reported in 21 studies, with pooled analysis confirming a similar result (mean difference: 1.56, 95% CI: 1.43–1.68, p < 0.01) (Figures 2A,B). To visualize data distribution and assess potential publication bias, funnel plots were created for the pooled BBB scores at both initial and final measurements (Figures 3A,B). These analyses reinforced the robustness of the findings while underscoring the importance of considering potential biases in interpreting the results.

Figure 2

Figure 2. (A) Pooled-analysis of Basso, Beattie, and Bresnahan scale at the first measurement after SCI. (B) Pooled-analysis of Basso, Beattie, and Bresnahan scale at the last measurement after SCI. CI, confidence interval; MD, mean difference; SCI, spinal cord injury; SD, standard difference.

Figure 3

Figure 3. (A) Funnel plot for asymmetry of pooled analysis of BBB at the first measurement. (B) Funnel plot for asymmetry of pooled analysis of BBB at the last measurement. BBB, Basso-Beattie-Bresnahan scale.

3.4 Bias of included studies

Using SYRCLE’s comprehensive evaluation tool, the quality of the included articles. Our analysis was assessed and revealed that most studies adhered strongly to standards of randomization and blinding protocols, with only a few reporting issues in either randomization or blinding. Notably, other potential biases were minimal across the reviewed literature. To provide a well-rounded view of potential publication biases, the findings are visually presented in Figure 4. This evaluation demonstrates the methodological rigor of the included studies while also identifying biases that should be considered when interpreting the present results.

Figure 4

Figure 4. Results from the SYRCLE risk of bias tool.

4 Discussion

Exosomes derived from various stem cell sources have gained prominence in experimental SCI treatment due to their ability to overcome limitations inherent in traditional stem cell therapies (45). In this comprehensive analysis of 21 selected studies, the efficacy of exosomes compared to placebo was rigorously evaluated. The results revealed a significant improvement in motor function in SCI-afflicted rats treated with MSC-exos across multiple time points. Notably, the therapeutic effects of MSC-exos were most pronounced within the first four weeks post-administration, indicating sustained and robust efficacy. This result suggested a potential mechanism for their prolonged therapeutic impact – possibly due to their extended presence at the SCI site. These findings also indicate the promise of exosome-based therapies for SCI management and provide valuable insights into the temporal dynamics of their effects, guiding future research and clinical translation efforts.

Recent findings align with two prior meta-analyses that explored the therapeutic potential of stem cell-derived exosomes in rodent models of SCI. Yi and colleagues conducted a systematic review of studies up to January 2021, covering 35 articles with 699 rodents. Their analysis showed significant motor function improvement in SCI rodents treated with stem cell-derived exosomes, with slower recovery observed in compression injuries compared to contusion and transection injuries post-exosome therapy (46). Similarly, Shang et al. conducted a network meta-analysis of pooled data from 40 preclinical studies through March 2023, focusing on the efficacy of stem cell-derived exosomes in SCI rat models; however, they found no significant differences in therapeutic outcomes across various MSC-exos at different treatment time points (47). Unlike these studies, the present meta-analysis concentrated on rat models of SCI induced specifically by contusion, reflecting the most common clinical scenario characterized by maximal irreversible neurological deficit. To strengthen the findings, included only studies using a single-vertebral injury model were included, thereby reducing potential heterogeneity and enhancing the relevance of the results.

Numerous preclinical studies have highlighted the promising therapeutic potential of stem cell-derived exosomes for treating SCI (48). However, before advancing this cell-free, exosome-based therapy to clinical trials, critical questions regarding therapeutic efficacy and safety must be thoroughly addressed. Chief among these concerns is identifying the optimal exosome source, as exosomes from different stem cell origins exhibit varying therapeutic potentials. To date, experimental SCI treatments have primarily used exosomes derived from various MSC sources, including bone marrow, umbilical cord, and adipose tissue (49). Notably, no studies have directly compared the therapeutic efficacy of exosomes from these different stem cell sources. To address this gap, a network meta-analysis was employed to assess comprehensively the therapeutic potential of exosomes from diverse origins. Our analysis found no statistically significant differences in SCI improvement efficacy among exosomes from the four distinct sources. While these findings align with the meta-analysis by Shang et al., they contrast with Liu et al., who suggested that umbilical cord-derived MSCs might be an optimal source, citing their availability and ethical advantages. Importantly, indirect comparisons across separate studies cannot serve as definitive evidence for the differential efficacy of exosomes from various sources in SCI treatment (50). Further rigorous research, including direct comparative studies, is essential to gain conclusive insights into this critical aspect of exosome-based therapy.

While existing evidence highlights the therapeutic potential of stem cell-derived exosomes in SCI repair, significant challenges remain before clinical application is feasible. Foremost, the complex molecular mechanisms underlying exosome synthesis, secretion and cellular uptake are not yet fully understood, warranting further research (51). Additionally, the methods for isolating, purifying, identifying and scaling exosome production need refinement, as recent studies have suggested (52). Precise quantification of MSC-exos and a deeper understanding of biological modifications to enhance their therapeutic efficacy are essential areas for ongoing investigation (53). Selecting optimal administration methods to improve both the efficacy and safety of MSC-exos is another critical area for innovation (54). Preclinical studies remain indispensable for evaluating MSC-exos’ effectiveness in SCI repair, identifying key therapeutic targets and pathways, and optimizing exosome sources (55).

Addressing the limitations inherent in the present study is essential. The predominance of positive results across studies raises concerns about potential publication bias, as negative findings may be concealed or unpublished, leading to potentially misleading conclusions. Additionally, the fundamental differences between animal studies and randomized clinical trials pose challenges in collecting detailed data for each experimental group; key details such as SCI severity, model dosage and administration methods were frequently missing, complicating data synthesis and interpretation. Variations in MSC-exos dosages and administration frequencies across studies introduce further bias, as these factors significantly influence therapeutic outcomes but are inconsistently standardized or reported. Differences in exosome extraction methods also affect exosome composition and efficacy, adding another layer of variability that hampers result comparability. Ambiguities and incomplete data were common; some studies reported only exosome volume or concentration, while four did not specify the injured spinal cord segment. Small sample sizes, particularly in studies involving mice, necessitate caution in interpreting locomotor recovery outcomes. Additionally, subjective interpretation introduces variability, as outcomes may be affected by observer bias and blinding status. Consequently, while the present findings provide valuable insights, translating them into actionable conclusions must be approached with due caution and consideration of these limitations.

In conclusion, MSC-exos show substantial therapeutic efficacy in improving motor function in rats with SCI, with bone marrow MSC-exos exhibiting particularly notable potential. However, reliance on animal studies, which are generally lower in evidence quality, introduces some uncertainty regarding the robustness and reliability of these findings. This highlights the need for high-quality, direct comparative studies to clarify the nuances of exosome-based therapy, identify the optimal stem cell sources, and strengthen confidence in its translational potential for SCI management.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding authors.

Author contributions

CM: Conceptualization, Data curation, Investigation, Visualization, Writing – original draft. ZX: Conceptualization, Formal analysis, Investigation, Visualization, Writing – original draft. XW: Data curation, Formal analysis, Visualization, Writing – review & editing. XD: Data curation, Visualization, Writing – review & editing. JW: Conceptualization, Formal analysis, Funding acquisition, Project administration, Supervision, Visualization, Writing – original draft, Writing – review & editing. CZ: Conceptualization, Data curation, Funding acquisition, Investigation, Project administration, Supervision, Visualization, Writing – original draft, Writing – review & editing. YX: Conceptualization, Data curation, Funding acquisition, Investigation, Project administration, Supervision, Visualization, Writing – original draft, Writing – review & editing.

Funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by National Key Research and Development Project of Stem Cell and Transformation Research (2019YFA0112100), the National Key R&D Program of China (2023YFC2506100), and Nanjing Science and Technology Foundation (202305002). The funders were not involved in the study design, collection, analysis, interpretation of data, the writing of this article or the decision to submit it for publication.

Conflict of interest

CM, XW, and YX were employed by Tianjin Everunion Biotechnology Co., Ltd. JW was employed by HELP Therapeutics Co., Ltd.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Quadri, SA, Farooqui, M, Ikram, A, Zafar, A, Khan, MA, Suriya, SS, et al. Recent update on basic mechanisms of spinal cord injury. Neurosurg Rev. (2020) 43:425–41. doi: 10.1007/s10143-018-1008-3

PubMed Abstract | Crossref Full Text | Google Scholar

2. Barbiellini Amidei, C, Salmaso, L, Bellio, S, and Saia, M. Epidemiology of traumatic spinal cord injury: a large population-based study. Spinal Cord. (2022) 60:812–9. doi: 10.1038/s41393-022-00795-w

PubMed Abstract | Crossref Full Text | Google Scholar

3. Anjum, A, Yazid, MD, Fauzi Daud, M, Idris, J, Ng, AMH, Selvi Naicker, A, et al. Spinal cord injury: pathophysiology, multimolecular interactions, and underlying recovery mechanisms. Int J Mol Sci. (2020) 21:7533. doi: 10.3390/ijms21207533

PubMed Abstract | Crossref Full Text | Google Scholar

4. Alizadeh, A, Dyck, SM, and Karimi-Abdolrezaee, S. Traumatic spinal cord injury: an overview of pathophysiology, models and acute injury mechanisms. Front Neurol. (2019) 10:282. doi: 10.3389/fneur.2019.00282

PubMed Abstract | Crossref Full Text | Google Scholar

5. Khaing, ZZ, Chen, JY, Safarians, G, Ezubeik, S, Pedroncelli, N, Duquette, RD, et al. Clinical trials targeting secondary damage after traumatic spinal cord injury. Int J Mol Sci. (2023) 24:3824. doi: 10.3390/ijms24043824

PubMed Abstract | Crossref Full Text | Google Scholar

6. Tabarestani, TQ, Lewis, NE, Kelly-Hedrick, M, Zhang, N, Cellini, BR, Marrotte, EJ, et al. Surgical considerations to improve recovery in acute spinal cord injury. Neurospine. (2022) 19:689–702. doi: 10.14245/ns.2244616.308

PubMed Abstract | Crossref Full Text | Google Scholar

7. Almeida, C, and Monteiro-Soares, M. Fernandes Â. Should non-pharmacological and non-surgical interventions be used to manage neuropathic pain in adults with spinal cord injury? – a systematic review. J Pain. (2022) 23:1510–29. doi: 10.1016/j.jpain.2022.03.239

PubMed Abstract | Crossref Full Text | Google Scholar

8. Tian, T, Zhang, S, and Yang, M. Recent Progress and challenges in the treatment of spinal cord injury. Protein Cell. (2023) 14:635–52. doi: 10.1093/procel/pwad003

PubMed Abstract | Crossref Full Text | Google Scholar

9. Assinck, P, Duncan, GJ, Hilton, BJ, Plemel, JR, and Tetzlaff, W. Cell transplantation therapy for spinal cord injury. Nat Neurosci. (2017) 20:637–47. doi: 10.1038/nn.4541

PubMed Abstract | Crossref Full Text | Google Scholar

10. Nandoe Tewarie, RS, Hurtado, A, Bartels, RH, Grotenhuis, A, and Oudega, M. Stem cell-based therapies for spinal cord injury. J Spinal Cord Med. (2009) 32:105–14. doi: 10.1080/10790268.2009.11760761

PubMed Abstract | Crossref Full Text | Google Scholar

11. Shang, Z, Wang, M, Zhang, B, Wang, X, and Wanyan, P. Clinical translation of stem cell therapy for spinal cord injury still premature: results from a single-arm Meta-analysis based on 62 clinical trials. BMC Med. (2022) 20:284. doi: 10.1186/s12916-022-02482-2

PubMed Abstract | Crossref Full Text | Google Scholar

12. Khan, SI, Ahmed, N, Ahsan, K, Abbasi, M, Maugeri, R, Chowdhury, D, et al. An insight into the prospects and drawbacks of stem cell therapy for spinal cord injuries: ongoing trials and future directions. Brain Sci. (2023) 13:1697. doi: 10.3390/brainsci13121697

PubMed Abstract | Crossref Full Text | Google Scholar

13. Zhang, K, and Cheng, K. Stem cell-derived exosome versus stem cell therapy. Nat Rev Bioeng. (2023) 1:608–9. doi: 10.1038/s44222-023-00064-2

PubMed Abstract | Crossref Full Text | Google Scholar

14. Yuan, YG, Wang, JL, Zhang, YX, Li, L, Reza, A, and Gurunathan, S. Biogenesis, composition and potential therapeutic applications of mesenchymal stem cells derived exosomes in various diseases. Int J Nanomedicine. (2023) 18:3177–210. doi: 10.2147/ijn.S407029

PubMed Abstract | Crossref Full Text | Google Scholar

15. Lotfy, A, AboQuella, NM, and Wang, H. Mesenchymal stromal/stem cell (Msc)-derived exosomes in clinical trials. Stem Cell Res Ther. (2023) 14:66. doi: 10.1186/s13287-023-03287-7

PubMed Abstract | Crossref Full Text | Google Scholar

16. Tang, Y, Zhou, Y, and Li, HJ. Advances in mesenchymal stem cell exosomes: a review. Stem Cell Res Ther. (2021) 12:71. doi: 10.1186/s13287-021-02138-7

PubMed Abstract | Crossref Full Text | Google Scholar

17. Kou, M, Huang, L, Yang, J, Chiang, Z, Chen, S, Liu, J, et al. Mesenchymal stem cell-derived extracellular vesicles for immunomodulation and regeneration: a next generation therapeutic tool? Cell Death Dis. (2022) 13:580. doi: 10.1038/s41419-022-05034-x

PubMed Abstract | Crossref Full Text | Google Scholar

18. Kumar, MA, Baba, SK, Sadida, HQ, Marzooqi, SA, Jerobin, J, Altemani, FH, et al. Extracellular vesicles as tools and targets in therapy for diseases. Signal Transduct Target Ther. (2024) 9:27. doi: 10.1038/s41392-024-01735-1

PubMed Abstract | Crossref Full Text | Google Scholar

19. Hwang, J, Jang, S, Kim, C, Lee, S, and Jeong, HS. Role of stem cell-derived exosomes and Micrornas in spinal cord injury. Int J Mol Sci. (2023) 24:13849. doi: 10.3390/ijms241813849

PubMed Abstract | Crossref Full Text | Google Scholar

20. Page, MJ, Moher, D, Bossuyt, PM, Boutron, I, Hoffmann, TC, Mulrow, CD, et al. Prisma 2020 explanation and elaboration: updated guidance and exemplars for reporting systematic reviews. BMJ. (2021) 372:n160. doi: 10.1136/bmj.n160

PubMed Abstract | Crossref Full Text | Google Scholar

21. Barros Filho, TE, and Molina, AE. Analysis of the sensitivity and reproducibility of the basso, Beattie, Bresnahan (Bbb) scale in Wistar rats. Clinics (Sao Paulo). (2008) 63:103–8. doi: 10.1590/s1807-59322008000100018

PubMed Abstract | Crossref Full Text | Google Scholar

22. Saginur, M, Fergusson, D, Zhang, T, Yeates, K, Ramsay, T, Wells, G, et al. Journal impact factor, trial effect size, and methodological quality appear scantly related: a systematic review and Meta-analysis. Syst Rev. (2020) 9:53. doi: 10.1186/s13643-020-01305-w

PubMed Abstract | Crossref Full Text | Google Scholar

23. Scheff, SW, Saucier, DA, and Cain, ME. A statistical method for analyzing rating scale data: the Bbb locomotor score. J Neurotrauma. (2002) 19:1251–60. doi: 10.1089/08977150260338038

PubMed Abstract | Crossref Full Text | Google Scholar

24. Afsartala, Z, Hadjighassem, M, Shirian, S, Ebrahimi-Barough, S, Gholami, L, Parsamanesh, G, et al. The effect of collagen and fibrin hydrogels encapsulated with adipose tissue mesenchymal stem cell-derived exosomes for treatment of spinal cord injury in a rat model. Iran J Biotechnol. (2023) 21:e3505. doi: 10.30498/ijb.2023.362229.3505

PubMed Abstract | Crossref Full Text | Google Scholar

25. Chang, Q, Hao, Y, Wang, Y, Zhou, Y, Zhuo, H, and Zhao, G. Bone marrow mesenchymal stem cell-derived Exosomal Microrna-125a promotes M2 macrophage polarization in spinal cord injury by downregulating Irf5. Brain Res Bull. (2021) 170:199–210. doi: 10.1016/j.brainresbull.2021.02.015

PubMed Abstract | Crossref Full Text | Google Scholar

26. Chen, Y, Tian, Z, He, L, Liu, C, Wang, N, Rong, L, et al. Exosomes derived from Mir-26a-modified Mscs promote axonal regeneration via the Pten/Akt/Mtor pathway following spinal cord injury. Stem Cell Res Ther. (2021) 12:224. doi: 10.1186/s13287-021-02282-0

PubMed Abstract | Crossref Full Text | Google Scholar

27. Cheshmi, H, Mohammadi, H, Akbari, M, Nasiry, D, Rezapour-Nasrabad, R, Bagheri, M, et al. Human placental mesenchymal stem cell-derived exosomes in combination with hyperbaric oxygen synergistically promote recovery after spinal cord injury in rats. Neurotox Res. (2023) 41:431–45. doi: 10.1007/s12640-023-00649-0

PubMed Abstract | Crossref Full Text | Google Scholar

28. Huang, W, Qu, M, Li, L, Liu, T, Lin, M, and Yu, X. Sirna in Msc-derived exosomes silences Ctgf Gene for locomotor recovery in spinal cord injury rats. Stem Cell Res Ther. (2021) 12:334. doi: 10.1186/s13287-021-02401-x

PubMed Abstract | Crossref Full Text | Google Scholar

29. Huang, W, Lin, M, Yang, C, Wang, F, Zhang, M, Gao, J, et al. Rat bone mesenchymal stem cell-derived exosomes loaded with Mir-494 promoting Neurofilament regeneration and behavioral function recovery after spinal cord injury. Oxidative Med Cell Longev. (2021) 2021:1634917. doi: 10.1155/2021/1634917

PubMed Abstract | Crossref Full Text | Google Scholar

30. Jiang, Z, and Zhang, J. Mesenchymal stem cell-derived exosomes containing Mir-145-5p reduce inflammation in spinal cord injury by regulating the Tlr4/Nf-Κb signaling pathway. Cell Cycle. (2021) 20:993–1009. doi: 10.1080/15384101.2021.1919825

PubMed Abstract | Crossref Full Text | Google Scholar

31. Kang, J, and Guo, Y. Human umbilical cord mesenchymal stem cells derived exosomes promote neurological function recovery in a rat spinal cord injury model. Neurochem Res. (2022) 47:1532–40. Epub 20220208. doi: 10.1007/s11064-022-03545-9

PubMed Abstract | Crossref Full Text | Google Scholar

32. Liu, J, Lin, M, Qiao, F, and Zhang, C. Exosomes derived from Lncrna Tctn2-modified mesenchymal stem cells improve spinal cord injury by Mir-329-3p/Igf1r Axis. J Mol Neurosci. (2022) 72:482–95. doi: 10.1007/s12031-021-01914-7

PubMed Abstract | Crossref Full Text | Google Scholar

33. Liu, W, Rong, Y, Wang, J, Zhou, Z, Ge, X, Ji, C, et al. Exosome-shuttled Mir-216a-5p from hypoxic preconditioned mesenchymal stem cells repair traumatic spinal cord injury by shifting microglial M1/M2 polarization. J Neuroinflammation. (2020) 17:47. doi: 10.1186/s12974-020-1726-7

PubMed Abstract | Crossref Full Text | Google Scholar

34. Mu, J, Wu, J, Cao, J, Ma, T, Li, L, Feng, S, et al. Rapid and effective treatment of traumatic spinal cord injury using stem cell derived exosomes. Asian J Pharm Sci. (2021) 16:806–15. doi: 10.1016/j.ajps.2021.10.002

PubMed Abstract | Crossref Full Text | Google Scholar

35. Nakazaki, M, Morita, T, Lankford, KL, Askenase, PW, and Kocsis, JD. Small extracellular vesicles released by infused mesenchymal stromal cells target M2 macrophages and promote Tgf-Β upregulation, microvascular stabilization and functional recovery in a rodent model of severe spinal cord injury. J Extracell Vesicles. (2021) 10:e12137. doi: 10.1002/jev2.12137

PubMed Abstract | Crossref Full Text | Google Scholar

36. Romanelli, P, Bieler, L, Scharler, C, Pachler, K, Kreutzer, C, Zaunmair, P, et al. Extracellular vesicles can deliver anti-inflammatory and anti-scarring activities of mesenchymal stromal cells after spinal cord injury. Front Neurol. (2019) 10:1225. doi: 10.3389/fneur.2019.01225

PubMed Abstract | Crossref Full Text | Google Scholar

37. Shao, Y, Wang, Q, Liu, L, Wang, J, and Wu, M. Alleviation of spinal cord injury by Microrna 137-overexpressing bone marrow mesenchymal stem cell-derived exosomes. Tohoku J Exp Med. (2023) 259:237–46. doi: 10.1620/tjem.2022.J118

PubMed Abstract | Crossref Full Text | Google Scholar

38. Sung, SE, Seo, MS, Kim, YI, Kang, KK, Choi, JH, Lee, S, et al. Human epidural ad-Msc exosomes improve function recovery after spinal cord injury in rats. Biomedicines. (2022) 10:678. doi: 10.3390/biomedicines10030678

PubMed Abstract | Crossref Full Text | Google Scholar

39. Wang, Y, Lai, X, Wu, D, Liu, B, Wang, N, and Rong, L. Umbilical mesenchymal stem cell-derived exosomes facilitate spinal cord functional recovery through the Mir-199a-3p/145-5p-mediated Ngf/Trka signaling pathway in rats. Stem Cell Res Ther. (2021) 12:117. doi: 10.1186/s13287-021-02148-5

PubMed Abstract | Crossref Full Text | Google Scholar

40. Wang, L, Pei, S, Han, L, Guo, B, Li, Y, Duan, R, et al. Mesenchymal stem cell-derived exosomes reduce A1 astrocytes via downregulation of phosphorylated Nfκb P65 subunit in spinal cord injury. Cell Physiol Biochem. (2018) 50:1535–59. doi: 10.1159/000494652

PubMed Abstract | Crossref Full Text | Google Scholar

41. Xue, C, Ma, X, Guan, X, Feng, H, Zheng, M, and Yang, X. Small extracellular vesicles derived from umbilical cord mesenchymal stem cells repair blood-spinal cord barrier disruption after spinal cord injury through down-regulation of Endothelin-1 in rats. PeerJ. (2023) 11:e16311. doi: 10.7717/peerj.16311

PubMed Abstract | Crossref Full Text | Google Scholar

42. Zhang, M, Wang, L, Huang, S, and He, X. Exosomes with high level of Mir-181c from bone marrow-derived mesenchymal stem cells inhibit inflammation and apoptosis to alleviate spinal cord injury. J Mol Histol. (2021) 52:301–11. doi: 10.1007/s10735-020-09950-0

PubMed Abstract | Crossref Full Text | Google Scholar

43. Zhou, Y, Wen, LL, Li, YF, Wu, KM, Duan, RR, Yao, YB, et al. Exosomes derived from bone marrow mesenchymal stem cells protect the injured spinal cord by inhibiting Pericyte Pyroptosis. Neural Regen Res. (2022) 17:194–202. doi: 10.4103/1673-5374.314323

PubMed Abstract | Crossref Full Text | Google Scholar

44. Zhou, W, Silva, M, Feng, C, Zhao, S, Liu, L, Li, S, et al. Exosomes derived from human placental mesenchymal stem cells enhanced the recovery of spinal cord injury by activating endogenous neurogenesis. Stem Cell Res Ther. (2021) 12:174. doi: 10.1186/s13287-021-02248-2

PubMed Abstract | Crossref Full Text | Google Scholar

45. Álvarez-Viejo, M. Mesenchymal stem cells from different sources and their derived exosomes: a pre-clinical perspective. World J Stem Cells. (2020) 12:100–9. doi: 10.4252/wjsc.v12.i2.100

PubMed Abstract | Crossref Full Text | Google Scholar

46. Yi, H, and Wang, Y. A Meta-analysis of exosome in the treatment of spinal cord injury. Open Med (Wars). (2021) 16:1043–60. doi: 10.1515/med-2021-0304

PubMed Abstract | Crossref Full Text | Google Scholar

47. Shang, Z, Wanyan, P, Wang, M, Zhang, B, Cui, X, and Wang, X. Stem cell-derived exosomes for traumatic spinal cord injury: a systematic review and network Meta-analysis based on a rat model. Cytotherapy. (2024) 26:1–10. doi: 10.1016/j.jcyt.2023.09.002

PubMed Abstract | Crossref Full Text | Google Scholar

48. Zhang, C, Deng, R, Zhang, G, He, X, Chen, H, Chen, B, et al. Therapeutic effect of exosomes derived from stem cells in spinal cord injury: a systematic review based on animal studies. Front Neurol. (2022) 13:847444. doi: 10.3389/fneur.2022.847444

PubMed Abstract | Crossref Full Text | Google Scholar

49. Han, C, Sun, X, Liu, L, Jiang, H, Shen, Y, Xu, X, et al. Exosomes and their therapeutic potentials of stem cells. Stem Cells Int. (2016) 2016:7653489. doi: 10.1155/2016/7653489

PubMed Abstract | Crossref Full Text | Google Scholar

50. Li, T, Puhan, MA, Vedula, SS, Singh, S, and Dickersin, K. Network Meta-analysis-highly attractive but more methodological research is needed. BMC Med. (2011) 9:79. doi: 10.1186/1741-7015-9-79

PubMed Abstract | Crossref Full Text | Google Scholar

51. Gurung, S, Perocheau, D, Touramanidou, L, and Baruteau, J. The exosome journey: from biogenesis to uptake and intracellular Signalling. Cell Commun Signal. (2021) 19:47. doi: 10.1186/s12964-021-00730-1

PubMed Abstract | Crossref Full Text | Google Scholar

52. Akbar, A, Malekian, F, Baghban, N, Kodam, SP, and Ullah, M. Methodologies to isolate and purify clinical grade extracellular vesicles for medical applications. Cells. (2022) 11:186. doi: 10.3390/cells11020186

PubMed Abstract | Crossref Full Text | Google Scholar

53. Avgoulas, DI, Tasioulis, KS, Papi, RM, and Pantazaki, AA. Therapeutic and diagnostic potential of exosomes as drug delivery Systems in Brain Cancer. Pharmaceutics. (2023) 15:1439. doi: 10.3390/pharmaceutics15051439

PubMed Abstract | Crossref Full Text | Google Scholar

54. Zeng, H, Guo, S, Ren, X, Wu, Z, Liu, S, and Yao, X. Current strategies for exosome cargo loading and targeting delivery. Cells. (2023) 12:1416. doi: 10.3390/cells12101416

PubMed Abstract | Crossref Full Text | Google Scholar

55. Krylova, SV, and Feng, D. The machinery of exosomes: biogenesis, release, and uptake. Int J Mol Sci. (2023) 24:1337. doi: 10.3390/ijms24021337

PubMed Abstract | Crossref Full Text | Google Scholar