Allergy and Immunology 2018
DOI: 10.1183/13993003.congress-2018.oa1653
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Systemic immunological changes following intravenous mesenchymal stromal cell infusion in stable COPD patients

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Cited by 3 publications
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“…In recent years, several approaches have been proposed to improve the effectiveness, endurance and therapeutic efficiency of MSCs [28,29]. Worth mentioning, the approaches utilizing MSCs, and especially the primed MSCs, could be vital for the success of cell therapy in lung complications, as the intravenously infused MSCs often get trapped in the lung; however, the retention time of MSCs within the lung is extremely short [30]. Though, the alteration in holding capacity of lung in a diseased scenario cannot be ruled out.…”
mentioning
confidence: 99%
“…In recent years, several approaches have been proposed to improve the effectiveness, endurance and therapeutic efficiency of MSCs [28,29]. Worth mentioning, the approaches utilizing MSCs, and especially the primed MSCs, could be vital for the success of cell therapy in lung complications, as the intravenously infused MSCs often get trapped in the lung; however, the retention time of MSCs within the lung is extremely short [30]. Though, the alteration in holding capacity of lung in a diseased scenario cannot be ruled out.…”
mentioning
confidence: 99%
“…Future therapies might enable the normalization of the diseased matrix, a particular problem in the context of cell therapy as delivering cells to a disease niche may limit the efficiency of engraftment and the efficacy of therapies. There is some evidence for this concept from in vitro studies of recellularized lung scaffolds, where donor age and disease status affects the efficiency of re-seeding (65) and from MSC infusions in patients, where lungs with milder disease retain MSCs for longer (66).…”
Section: Future Cell Therapies For Lung Diseasementioning
confidence: 99%
“…Following systemic administration, MSCs primarily lodge in the pulmonary capillary system, through as yet poorly understood interactions with the endothelium. They do not engraft and are cleared by a range of host immune mechanisms over 1-2 days, although available data suggests that they may persist for up to 3-4 days in the setting of lung inflammation (Allers et al, 2004;Armitage et al, 2018). MSCs express a range of danger and molecular pathogen cell surface receptors, including the Toll-Like receptors and a growing body of literature demonstrates that while in the pulmonary capillary bed, the MSCs respond to specific inflammatory environments by releasing different portfolios of mediators (Romieu-Mourez et al, 2009;Waterman et al, 2010;Kusuma et al, 2017;Abreu et al, 2019;Islam et al, 2019;Enes et al, 2021;Galipeau et al, 2021).…”
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confidence: 99%