2018
DOI: 10.1002/bit.26532
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Precision‐porous templated scaffolds of varying pore size drive dendritic cell activation

Abstract: Scaffold based systems have shown significant potential in modulating immune responses in vivo. While there has been much attention on macrophage interactions with tissue engineered scaffolds for tissue regeneration, fewer studies have looked at the effects of scaffold design on the response of immune cells−that is, dendritic cells (DCs). Here, we present the effects of varying pore size of poly (2-hydroxyethyl methacrylate) (pHEMA) and poly(dimethylsiloxane) (PDMS, silicone) scaffolds on the maturation and in… Show more

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Cited by 28 publications
(31 citation statements)
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References 36 publications
(47 reference statements)
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“…Based on our positive results, the chitosan‐alginate gel scaffold could be a suitable candidate for a subcutaneous delivery system of mRNA vaccines. Various scaffolds have been developed and widely used on for cell modification, tissue regeneration, and drug or gene delivery, but none of them considered nucleic acid vaccine loading and delivery.…”
Section: Discussionmentioning
confidence: 99%
“…Based on our positive results, the chitosan‐alginate gel scaffold could be a suitable candidate for a subcutaneous delivery system of mRNA vaccines. Various scaffolds have been developed and widely used on for cell modification, tissue regeneration, and drug or gene delivery, but none of them considered nucleic acid vaccine loading and delivery.…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, structures with sharper pore size distributions seem to enhance tissue ingrowth in vivo [ 208 ]. Furthermore, dendritic cell maturation was found to be higher in scaffolds with pore diameter of 40 µm compared to 90 µm, which led to a collagenous and avascular tissue [ 209 ]. Accordingly, the suitable range regarding the pore size seems to follow the same trend in vivo and in vitro , namely, few hundreds of microns, while positive outcomes regarding immune cell maturation occur preferably for pore size below 100 µm.…”
Section: In Vivo Outcomes and Clinical Trialsmentioning
confidence: 99%
“…The design of these cancer vaccine scaffolds must address several engineering criteria: first, the scaffold should contain chemical signals, such as cytokines or chemokines, that enable DC recruitment[296]. Additionally, a 3D macroporous structure is required that enables DC infiltration[297]. After infiltration, DCs need to be able to uptake antigen within the scaffold and undergo maturation.…”
Section: Biomaterials Scaffolds For Localized Vaccine Deliverymentioning
confidence: 99%