dc.creator | Saksida, Tamara | |
dc.creator | Jevtić, Bojan | |
dc.creator | Nikolovski, Neda | |
dc.creator | Miljković, Đorđe | |
dc.creator | Stojanović, Ivana D. | |
dc.date.accessioned | 2020-07-10T12:16:07Z | |
dc.date.available | 2021-06-17 | |
dc.date.available | 2021-06-17 | |
dc.date.issued | 2021 | |
dc.identifier.issn | 1523-0864 | |
dc.identifier.uri | https://radar.ibiss.bg.ac.rs/handle/123456789/3766 | |
dc.description.abstract | Significance: Autoimmune diseases are progressively affecting westernized societies, as
the proportion of individuals suffering from autoimmunity is steadily increasing over the
past decades. Understanding the role of reactive oxygen species (ROS) in modulation of
the immune response in the pathogenesis of autoimmune disorders is of utmost
importance. The focus of this review is the regulation of ROS production within tolerogenic
dendritic cells (tolDC) and regulatory T (Treg) cells that have the essential role in the
prevention of autoimmune diseases and significant potency in their therapy.
Recent Advances: It is now clear that ROS are extremely important for the proper function
of both DC and T cells. Antigen processing/presentation and the ability of DC to activate T
cells depend upon the ROS availability. Treg differentiation, suppressive function and
stability are profoundly influenced by ROS presence.
Critical Issues: Although a plethora of results on the relation between ROS and immune
cells exists, it remains unclear whether ROS modulation is a productive way for skewing T
cells and DC towards a tolerogenic phenotype. Also, the possibility of ROS modulation for
enhancement of regulatory properties of DC and Treg during their preparation for use in
cellular therapy has to be clarified.
Future Directions: Studies of DC and T cell redox regulation should allow for the
improvement of the therapy of autoimmune diseases. This could be achieved through the
direct therapeutic application of ROS modulators in autoimmunity or indirectly, through
ROS-dependent enhancement of tolDC and Treg preparation for cell-based
immunotherapy. | en |
dc.language.iso | en | sr |
dc.publisher | Mary Ann Liebert, Inc. | sr |
dc.relation | info:eu-repo/grantAgreement/MESTD/inst-2020/200007/RS// | sr |
dc.relation.isversionof | https://radar.ibiss.bg.ac.rs/handle/123456789/4234 | |
dc.rights | embargoedAccess | sr |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.source | Antioxidants & Redox Signaling | sr |
dc.subject | Reactive oxygen species | sr |
dc.subject | Dendritic cells | sr |
dc.subject | T cells | sr |
dc.subject | Tolerogenic dendritic cells | sr |
dc.subject | T regulatory cells | sr |
dc.title | Redox Regulation of Tolerogenic Dendritic Cells and Regulatory T Cells in the Pathogenesis and Therapy of Autoimmunity | en |
dc.type | article | sr |
dc.rights.license | BY | sr |
dcterms.abstract | Миљковић, Ђорђе; Стојановић, Ивана Д; Јевтић, Бојан; Саксида, Тамара; Ђедовић, Неда; | |
dc.rights.holder | © 2020, Mary Ann Liebert, Inc. | sr |
dc.citation.issue | 5 | |
dc.citation.volume | 34 | |
dc.description.note | Final publication is available from Mary Ann Liebert, Inc., publishers [http://dx.doi.org/10.1089/ars.2019.7999] | |
dc.identifier.doi | 10.1089/ars.2019.7999 | |
dc.identifier.pmid | 32458699 | |
dc.identifier.scopus | 2-s2.0-85099577648 | |
dc.identifier.wos | 000544296600001 | |
dc.citation.apa | Saksida, T., Jevtić, B., Djedović, N., Miljković, Đ., & Stojanović, I. (2021). Redox Regulation of Tolerogenic Dendritic Cells and Regulatory T Cells in the Pathogenesis and Therapy of Autoimmunity. Antioxidants & Redox Signaling, 34 (5) 364-382. | |
dc.citation.vancouver | Saksida T, Jevtić B, Djedović N, Miljković Đ, Stojanović I. Redox Regulation of Tolerogenic Dendritic Cells and Regulatory T Cells in the Pathogenesis and Therapy of Autoimmunity. Antioxid Redox Signal. 2021;34(5):364-82. | |
dc.citation.spage | 364 | |
dc.citation.epage | 382 | |
dc.type.version | acceptedVersion | sr |
dc.identifier.fulltext | https://radar.ibiss.bg.ac.rs/bitstream/id/6431/Saksida-et-al.pdf | |
dc.citation.rank | aM21 | |