Journal of Cell Science & Therapy

Journal of Cell Science & Therapy
Open Access

ISSN: 2157-7013

+44 1300 500008

Immunomodulatory mechanisms underlying the therapeutical effects of amniotic membrane-derived cells


5th World Congress on Cell & Stem Cell Research

March 23-25, 2015 DoubleTree by Hilton Chicago - North Shore, USA

Ornella Parolini

Scientific Tracks Abstracts: J Cell Sci Ther

Abstract :

The modern understanding of regenerative medicine focuses on the immunomodulatory potential of MSC, rather than their differentiation capability. In the complex scenario of stem cells, the human placenta has blossomed as an interesting source of therapeutic cells. Our group has pioneered the understanding of the immunomodulatory potential of cells isolated from human term placenta. We have previously described the ability of mesenchymal cells isolated from the amniotic membrane (hAMSC) to reduce T cell proliferation induced by alloantigens or mitogens, and their capability to block the differentiation of monocytes to dendritic cells. Recently, we demonstrated that primary and expanded hAMSC, cultured with monocytes in either contact or transwell settings, strongly inhibited the differentiation of DCs and induced a shift toward M2-like macrophages. This was observed even when medium conditioned by hAMSC (CM-hAMSC) was applied, but not when using cells isolated from the epithelial layer of the amniotic membrane (hAEC). We?ve also shown that monocytes co-cultured with hAMSC and hAEC possessed different secretomes. In a more recent study we showed that CM-hAMSC was able to equally suppress the proliferation of central and effector memory subsets of both CD4+ T-helper (Th) and CD8+ cytotoxic T-lymphocytes. CM-hAMSC induced significant changes in the phenotype of CD4+ cells, such as the reduced expression of markers associated to the Th1 and Th17 populations. Significant changes in cytokine secretion were also induced by CM-hAMSC. We also showed that CM-hAMSC significantly induced the Treg compartment, as shown by an induction of proliferating CD4+FoxP3+ cells and CD25+FoxP3+ and CD39+FoxP3+Treg and increased secretion of TGF-β. Taken together, these multifaceted, immunomodulatory properties of cells isolated from the amniotic membrane of human term placenta, and conditioned medium derived from cell culture, render them unique and attractive for their potential in a variety of applications, especially inflammatory diseases.

Biography :

Ornella Parolini is the Director of E. Menni Research Center, Fondazione Poliambulanza, Brescia, Italy and the President of IPLASS-International Placenta Stem Cell Society. She has pioneered research on human placenta-derived stem cells. Her research is focused on the immunomodulatory, anti-inflammatory and anti- fibrotic properties of amniotic and chorionic membrane-derivatives as amnion patches, amniotic cell subpopulations and their conditioned medium, as products applicable in regenerative medicine. She is author of over 100 publications in peer-reviewed journals as well as several book chapters. She also has several patent applications.

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