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March 25, 2026Advanced Science2 citationsOpen Access

Engineering Approaches to Modify Immunomodulatory Functions of Mesenchymal Stromal Cells (MSCs): Tissue Regeneration and Clinical Application

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SYSichen YangKLKejia LiNWNing Wang

Key Points

  • The aim is to explore current advancements in engineering mesenchymal stromal cells (MSCs) to improve their immunomodulatory functions for clinical applications.
  • Review of Phase III and IV clinical trials involving MSC therapies.
  • Discussion of challenges related to MSC clinical translation.
  • Overview of engineering strategies like genetic modification and biomaterial delivery systems.
  • Highlighting MSC-derived extracellular vesicles for enhanced paracrine signaling.
  • Examination of induced pluripotent stem cell-derived MSCs to reduce donor variability.
  • Engineering approaches can potentially overcome limitations of MSCs.
  • Inventive strategies enhance the immunomodulatory capabilities of MSCs.
  • Integration of these methods could significantly impact the treatment of inflammatory diseases.

Abstract

By virtue of their intrinsic immunomodulatory properties, mesenchymal stromal cells (MSCs) represent a promising therapeutic tool for immune-related disorders. Research findings support that MSCs are involved in complex inflammatory pathologies by interacting with local immune cells. In addition to their immunomodulation ability, MSCs also contribute to cell-mediated tissue regeneration due to their potential for multilineage differentiation. However, despite their accessibility, clinical translation of MSCs faces challenges, including their inherent heterogeneity, transient therapeutic effects, and microenvironment-dependent functionality. This review provides an overview of current advances in MSC-based therapies for immune-related disorders, emphasizing Phase III and IV clinical trials and therapies approved by global regulatory agencies. Additionally, we highlight innovative engineering strategies designed to address the limitations of MSCs while enhancing their immunomodulatory capabilities. These approaches include: (1) cell pre-treatment and genetic modification to improve therapeutic efficacy; (2) biomaterial-mediated delivery systems for targeted sites; (3) MSC-derived extracellular vesicle (EV)-based therapeutics to amplify paracrine signaling; (4) induced pluripotent stem cell (iPSC)-derived MSCs to overcome donor variability. By integrating these methodologies with ongoing clinical approaches, this review underscores the potential of engineered MSC immunomodulation in addressing inflammatory pathologies, bridging the gap between basic research and clinical application.

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Cite This Study

Yang et al. (2026) studied this question.

synapsesocial.com/papers/69c37bb3b34aaaeb1a67e523https://doi.org/10.1002/advs.202522601
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