| Literature DB >> 29490284 |
Raghavan Chinnadurai1, Devi Rajan2, Muna Qayed2, Dalia Arafat3, Marco Garcia4, Yifei Liu5, Subra Kugathasan2, Larry J Anderson2, Greg Gibson3, Jacques Galipeau6.
Abstract
Assays that can characterize MSC immune potency need to be identified for use in advanced clinical trials. MSCs possess a number of putative regenerative and immunomodulatory properties, and an assay matrix approach may best capture involved effector pathways. We have tested two assay systems to measure the potency of MSCs derived from human subjects: MSC secretome analysis and a quantitative RNA-based array for genes specific to immunomodulatory and homing properties of MSCs. Secretome analysis identified a unique cytokine signature that is upregulated by MSCs or downregulated in responder PBMCs and correlated with T cell suppression. Use of interferon-γ as a surrogate for the action of activated PBMCs on MSCs served as an alternative for the use of human PBMCs as responder cells in a potency assay. Our approach and results define and simplify the multifunctional or matrix responses of MSCs and may serve as a platform for robust potency analysis.Entities:
Keywords: PBMCs; assay matrix; interferon-γ; mesenchymal stromal cells; secretome; transcriptome
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Year: 2018 PMID: 29490284 PMCID: PMC5855117 DOI: 10.1016/j.celrep.2018.02.013
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423