Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/36154
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dc.contributor.authorBAETEN, Paulien-
dc.contributor.authorVAN ZEEBROECK, Lauren-
dc.contributor.authorKLEINEWIETFELD, Markus-
dc.contributor.authorHELLINGS, Niels-
dc.contributor.authorBROUX, Bieke-
dc.date.accessioned2021-12-13T12:50:50Z-
dc.date.available2021-12-13T12:50:50Z-
dc.date.issued2022-
dc.date.submitted2021-08-27T13:03:36Z-
dc.identifier.citationCLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 62 (2) ,p. 363-381-
dc.identifier.urihttp://hdl.handle.net/1942/36154-
dc.description.abstractAutoimmunity is caused by an unbalanced immune system, giving rise to a variety of organ-specific to system disorders. Patients with autoimmune diseases are commonly treated with broad-acting immunomodulatory drugs, with the risk of severe side effects. Regulatory T cells (Tregs) have the inherent capacity to induce peripheral tolerance as well as tissue regeneration and are therefore a prime candidate to use as cell therapy in patients with autoimmune disorders. (Pre)clinical studies using Treg therapy have already established safety and feasibility, and some show clinical benefits. However, Tregs are known to be functionally impaired in autoimmune diseases. Therefore, ex vivo manipulation to boost and stably maintain their suppressive function is necessary when considering autologous transplantation. Similar to autoimmunity, severe coronavirus disease 2019 (COVID-19) is characterized by an exaggerated immune reaction and altered Treg responses. In light of this, Treg-based therapies are currently under investigation to treat severe COVID-19. This review provides a detailed overview of the current progress and clinical challenges of Treg therapy for autoimmune and hyperinflammatory diseases, with a focus on recent successes of ex vivo Treg manipulation.-
dc.description.sponsorshipThe authors are funded by Fonds voor Wetenschappelijk Onderzoek (FWO), the Belgian Charcot Stichting, Stichting MS Research, MS International Foundation, and MoveS.-
dc.language.isoen-
dc.publisherHUMANA PRESS INC-
dc.rightsThe Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021-
dc.subject.otherRegulatory T cells-
dc.subject.otherCell therapy-
dc.subject.otherAutoimmunity-
dc.subject.otherCOVID-19-
dc.subject.otherGene editing-
dc.subject.otherRNA interference-
dc.titleImproving the Efficacy of Regulatory T Cell Therapy-
dc.typeJournal Contribution-
dc.identifier.epage381-
dc.identifier.issue2-
dc.identifier.spage363-
dc.identifier.volume62-
local.bibliographicCitation.jcatA1-
local.publisher.place999 RIVERVIEW DRIVE SUITE 208, TOTOWA, NJ 07512 USA-
local.type.refereedRefereed-
local.type.specifiedReview-
dc.identifier.doi10.1007/s12016-021-08866-1-
dc.identifier.pmid34224053-
dc.identifier.isi000669750200001-
local.provider.typeWeb of Science-
local.uhasselt.internationalyes-
item.contributorBAETEN, Paulien-
item.contributorVAN ZEEBROECK, Lauren-
item.contributorKLEINEWIETFELD, Markus-
item.contributorHELLINGS, Niels-
item.contributorBROUX, Bieke-
item.fullcitationBAETEN, Paulien; VAN ZEEBROECK, Lauren; KLEINEWIETFELD, Markus; HELLINGS, Niels & BROUX, Bieke (2022) Improving the Efficacy of Regulatory T Cell Therapy. In: CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 62 (2) ,p. 363-381.-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
item.validationecoom 2022-
crisitem.journal.issn1080-0549-
crisitem.journal.eissn1559-0267-
Appears in Collections:Research publications
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