Frontiers in Immunology (Sep 2022)

The short-term and long-term effects of intranasal mesenchymal stem cell administration to noninflamed mice lung

  • Marlena Tynecka,
  • Adrian Janucik,
  • Magdalena Niemira,
  • Arkadiusz Zbikowski,
  • Nino Stocker,
  • Agnieszka Tarasik,
  • Aleksandra Starosz,
  • Kamil Grubczak,
  • Anna Szalkowska,
  • Urszula Korotko,
  • Joanna Reszec,
  • Miroslaw Kwasniewski,
  • Adam Kretowski,
  • Adam Kretowski,
  • Cezmi Akdis,
  • Milena Sokolowska,
  • Marcin Moniuszko,
  • Marcin Moniuszko,
  • Andrzej Eljaszewicz

DOI
https://doi.org/10.3389/fimmu.2022.967487
Journal volume & issue
Vol. 13

Abstract

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Mesenchymal stem cells (mesenchymal stromal cells; MSC)-based therapies remain a promising approach to treat degenerative and inflammatory diseases. Their beneficial effects were confirmed in numerous experimental models and clinical trials. However, safety issues concerning MSCs’ stability and their long-term effects limit their implementation in clinical practice, including treatment of respiratory diseases such as asthma, chronic obstructive pulmonary disease, and COVID-19. Here, we aimed to investigate the safety of intranasal application of human adipose tissue-derived MSCs in a preclinical experimental mice model and elucidate their effects on the lungs. We assessed short-term (two days) and long-term (nine days) effects of MSCs administration on lung morphology, immune responses, epithelial barrier function, and transcriptomic profiles. We observed an increased frequency of IFNγ- producing T cells and a decrease in occludin and claudin 3 as a long-term effect of MSCs administration. We also found changes in the lung transcriptomic profiles, reflecting redox imbalance and hypoxia signaling pathway. Additionally, we found dysregulation in genes clustered in pattern recognition receptors, macrophage activation, oxidative stress, and phagocytosis. Our results suggest that i.n. MSCs administration to noninflamed healthy lungs induces, in the late stages, low-grade inflammatory responses aiming at the clearance of MSCs graft.

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