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Interleukin-2/anti-interleukin-2 immune complex attenuates cold ischemia-reperfusion injury after kidney transplantation by increasing renal regulatory T cells

Authors
 Joon Young Jang  ;  Hyung Woo Kim  ;  Ji-Jing Yan  ;  Tae Kyeom Kang  ;  Wook-Bin Lee  ;  Beom Seok Kim  ;  Jaeseok Yang 
Citation
 CLINICAL AND TRANSLATIONAL MEDICINE, Vol.14(3) : e1631, 2024-03 
Journal Title
DENTISTRY JOURNAL
Issue Date
2024-03
MeSH
Acute Kidney Injury* / drug therapy ; Acute Kidney Injury* / etiology ; Acute Kidney Injury* / metabolism ; Animals ; Antigen-Antibody Complex ; Antioxidants / pharmacology ; Fibrosis ; Interleukin-2 / metabolism ; Kidney ; Kidney Transplantation* / adverse effects ; Mice ; Reactive Oxygen Species / metabolism ; Reperfusion Injury* / drug therapy ; Reperfusion Injury* / metabolism ; T-Lymphocytes, Regulatory
Keywords
IL-2/anti-IL-2 immune complex ; cold ischemia-reperfusion injury ; kidney transplantation ; regulatory T cells
Abstract
BackgroundCold ischemia-reperfusion injury (IRI) is an unavoidable complication of kidney transplantation. We investigated the role of regulatory T cells (Treg) in cold IRI and whether the interleukin (IL)-2/anti-IL-2 antibody complex (IL-2C) can ameliorate cold IRI.MethodsWe developed a cold IRI mouse model using kidney transplantation and analyzed the IL-2C impact on cold IRI in acute, subacute and chronic phases.ResultsTreg transfer attenuated cold IRI, while Treg depletion aggravated cold IRI. Next, IL-2C administration prior to IRI mitigated acute renal function decline, renal tissue damage and apoptosis and inhibited infiltration of effector cells into kidneys and pro-inflammatory cytokine expression on day 1 after IRI. On day 7 after IRI, IL-2C promoted renal regeneration and reduced subacute renal damage. Furthermore, on day 28 following IRI, IL-2C inhibited chronic fibrosis. IL-2C decreased reactive oxygen species-mediated injury and improved antioxidant function. When IL-2C was administered following IRI, it also increased renal regeneration with Treg infiltration and suppressed renal fibrosis. In contrast, Treg depletion in the presence of IL-2C eliminated the positive effects of IL-2C on IRI.ConclusionTregs protect kidneys from cold IRI and IL-2C inhibited cold IRI by increasing the renal Tregs, suggesting a potential of IL-2C in treating cold IRI.Key Points Interleukin (IL)-2/anti-IL-2 antibody complex attenuated acute renal injury, facilitated subacute renal regeneration and suppressed chronic renal fibrosis after cold ischemia-reperfusion injury (IRI) by increasing the renal Tregs. IL-2/anti-IL-2 antibody complex decreased reactive oxygen species-mediated injury and improved antioxidant function. This study suggests the therapeutic potential of the IL-2/anti-IL-2 antibody complex in kidney transplantation-associated cold IR.,Interleukin (IL)-2/anti-IL-2 antibody complex attenuated acute renal injury, facilitated subacute renal regeneration and suppressed chronic renal fibrosis after cold ischemia-reperfusion injury (IRI) by increasing the renal Tregs. IL-2/anti-IL-2 antibody complex decreased reactive oxygen species-mediated injury and improved antioxidant function. This study suggests the therapeutic potential of the IL-2/anti-IL-2 antibody complex in kidney transplantation-associated cold IRI. image,
Files in This Item:
T202402322.pdf Download
DOI
10.1002/ctm2.1631
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Beom Seok(김범석) ORCID logo https://orcid.org/0000-0002-5732-2583
Kim, Hyung Woo(김형우) ORCID logo https://orcid.org/0000-0002-6305-452X
Yang, Jaeseok(양재석)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/199095
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