<?xml version="1.0"?>
<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Varicella-zoster virus recapitulates its immune evasive behaviour in matured hiPSC-derived neurospheroids</dc:title><dc:creator>Govaerts,	Jonas	(Avtor)
	</dc:creator><dc:creator>Van Breedam,	Elise	(Avtor)
	</dc:creator><dc:creator>Motaln,	Helena	(Avtor)
	</dc:creator><dc:creator>Rogelj,	Boris	(Avtor)
	</dc:creator><dc:creator>Ponsaerts,	Peter	(Avtor)
	</dc:creator><dc:subject>interferon signalling</dc:subject><dc:subject>neurospheroids</dc:subject><dc:subject>antigen presentation</dc:subject><dc:subject>stress granules</dc:subject><dc:subject>structural integrity</dc:subject><dc:description>Varicella-zoster virus (VZV) encephalitis and meningitis are potential central nervous system (CNS) complications following primary VZV infection or reactivation. With Type-I interferon (IFN) signalling being an important first line cellular defence mechanism against VZV infection by the peripheral tissues, we here investigated the triggering of innate immune responses in a human neural-like environment. For this, we established and characterised 5-month matured hiPSC-derived neurospheroids (NSPHs) containing neurons and astrocytes. Subsequently, NSPHs were infected with reporter strains of VZV (VZVeGFP-ORF23) or Sendai virus (SeVeGFP), with the latter serving as an immune-activating positive control. Live cell and immunocytochemical analyses demonstrated VZVeGFP-ORF23 infection throughout the NSPHs, while SeVeGFP infection was limited to the outer NSPH border. Next, NanoString digital transcriptomics revealed that SeVeGFP-infected NSPHs activated a clear Type-I IFN response, while this was not the case in VZVeGFP-ORF23-infected NSPHs. Moreover, the latter displayed a strong suppression of genes related to IFN signalling and antigen presentation, as further demonstrated by suppression of IL-6 and CXCL10 production, failure to upregulate Type-I IFN activated anti-viral proteins (Mx1, IFIT2 and ISG15), as well as reduced expression of CD74, a key-protein in the MHC class II antigen presentation pathway. Finally, even though VZVeGFP-ORF23-infection seems to be immunologically ignored in NSPHs, its presence does result in the formation of stress granules upon long-term infection, as well as disruption of cellular integrity within the infected NSPHs. Concluding, in this study we demonstrate that 5-month matured hiPSC-derived NSPHs display functional innate immune reactivity towards SeV infection, and have the capacity to recapitulate the strong immune evasive behaviour towards VZV.</dc:description><dc:publisher>Frontiers </dc:publisher><dc:date>2024</dc:date><dc:date>2025-01-08 12:37:14</dc:date><dc:type>Neznano</dc:type><dc:identifier>21153</dc:identifier><dc:identifier>UDK: 57</dc:identifier><dc:identifier>ISSN pri članku: 1664-3224</dc:identifier><dc:identifier>DOI: 10.3389/fimmu.2024.1458967</dc:identifier><dc:identifier>COBISS_ID: 207650563</dc:identifier><dc:source>Švica</dc:source><dc:language>sl</dc:language><dc:rights>© 2024 Govaerts, Van Breedam, De Beuckeleer, Goethals, D’Incal, Di Stefano, Van Calster, Buyle-Huybrecht, Boeren, De Reu, Paludan, Thiry, Lebrun, Sadzot-Delvaux, Motaln, Rogelj, Van Weyenbergh, De Vos, Vanden Berghe, Ogunjimi, Delputte and Ponsaerts.</dc:rights></metadata>
