Intrapericardial Delivery of Cardiosphere-Derived Cells: An Immunological Study in a Clinically Relevant Large Animal Model

PLoS One. 2016 Feb 11;11(2):e0149001. doi: 10.1371/journal.pone.0149001. eCollection 2016.

Abstract

Introduction: The intrapericardial delivery has been defined as an efficient method for pharmacological agent delivery. Here we hypothesize that intrapericardial administration of cardiosphere-derived cells (CDCs) may have an immunomodulatory effect providing an optimal microenvironment for promoting cardiac repair. To our knowledge, this is the first report studying the effects of CDCs for myocardial repair using the intrapericardial delivery route.

Material and methods: CDCs lines were isolated, expanded and characterized by flow cytometry and PCR. Their differentiation ability was determined using specific culture media and differential staining. 300,000 CDCs/kg were injected into the pericardial space of a swine myocardial infarcted model. Magnetic resonance imaging, biochemical analysis of pericardial fluid and plasma, cytokine measurements and flow cytometry analysis were performed.

Results: Our results showed that, phenotype and differentiation behavior of porcine CDCs were equivalent to previously described CDCs. Moreover, the intrapericardial administration of CDCs fulfilled the safety aspects as non-adverse effects were reported. Finally, the phenotypes of resident lymphocytes and TH1 cytokines in the pericardial fluid were significantly altered after CDCs administration.

Conclusions: The pericardial fluid could be considered as a safe and optimal vehicle for CDCs administration. The observed changes in the studied immunological parameters could exert a modulation in the inflammatory environment of infarcted hearts, indirectly benefiting the endogenous cardiac repair.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / cytology
  • Animals
  • Cell Differentiation
  • Cell Transplantation
  • Chondrocytes / cytology
  • Cytokines / metabolism
  • Disease Models, Animal
  • Flow Cytometry
  • Magnetic Resonance Imaging
  • Myocardial Infarction / immunology*
  • Myocardial Infarction / therapy*
  • Myocardium / pathology
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / immunology
  • Osteogenesis
  • Pericardium / metabolism*
  • Phenotype
  • Polymerase Chain Reaction
  • Regeneration
  • Stem Cell Transplantation / methods
  • Swine

Substances

  • Cytokines

Grants and funding

This work was supported in part by one grant from GobEx (Ayuda a grupos catalogados de la Junta de Extremadura, GR15175), two grants from Junta de Extremadura to JGC (TA13042 and IB13123 co-financed by FEDER/FSE) and two grants from Redes temáticas de investigación cooperativa en salud (RD12/0042/0025 to FMSM and CB).