Interleukin-10 and Transforming Growth Factor-β Cytokines Decrease Immune Activation During Normothermic Ex Vivo Machine Perfusion of the Rat Liver

被引:16
作者
Carlson, Kristin N. [1 ]
Pavan-Guimaraes, Juliana [1 ]
Verhagen, Joshua C. [1 ]
Chlebeck, Peter [1 ]
Verhoven, Bret [1 ]
Jennings, Heather [1 ]
Najmabadi, Feridoon [1 ]
Liu, Yongjun [2 ]
Burlingham, William [1 ]
Capitini, Christian M. [3 ,4 ]
Al-Adra, David P. [1 ,4 ]
机构
[1] Univ Wisconsin, Dept Surg, Div Transplantat, Sch Med & Publ Hlth, H4-750 CSC,600 Highland Ave, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Pathol & Lab Med, Sch Med & Publ Hlth, Madison, WI 53792 USA
[3] Univ Wisconsin, Dept Pediat, Sch Med & Publ Hlth, Carbone Canc Ctr, Madison, WI 53792 USA
[4] Univ Wisconsin, Carbone Canc Ctr, Sch Med & Publ Hlth, Madison, WI 53792 USA
关键词
TOLEROGENIC DENDRITIC CELLS; REPERFUSION INJURY; T-CELLS; TRANSPLANTATION; PRESERVATION; TOLERANCE; ISCHEMIA; IMPROVES; THERAPY; GRAFTS;
D O I
10.1002/lt.26206
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Normothermic ex vivo liver perfusion (NEVLP) is a novel system for organ preservation that may improve over static cold storage clinically and offers the chance for graft modification prior to transplantation. Although recent studies have shown the presence of inflammatory molecules during perfusion, none have yet shown the effects of NEVLP on liver-resident immune cell activation. We investigated the effects of NEVLP on liver-resident immune cell activation and assessed the ability of anti-inflammatory cytokines interleukin 10 (IL10) and transforming growth factor beta (TGF-beta) to improve organ function and reduce immune activation during perfusion. Rat livers were perfused for 4 hours at 37 degrees C with or without the addition of 20 ng/mL of each IL10 and TGF-beta (n = 7). Naive and cold storage (4 hours at 4 degrees C) livers served as controls (n = 4). Following preservation, gene expression profiles were assessed through single-cell RNA sequencing; dendritic cell and macrophage activation was measured by flow cytometry; and cytokine production was assessed by enzyme-linked immunosorbent assay. NEVLP induced a global inflammatory gene expression signature, most notably in liver-resident macrophages and dendritic cells, which was accompanied by an increase in cell-surface levels of major histocompatibility complex (MHC) II, CD40, and CD86. Immune activation was partially ameliorated by IL10 and TGF-beta treatment, but no changes were observed in inflammatory cytokine production. Overall levels of liver damage and cellular apoptosis from perfusion were low, and liver function was improved with IL10 and TGF-beta treatment. This is the first study to demonstrate that liver-resident immune cells gain an activated phenotype during NEVLP on both the gene and protein level and that this activation can be reduced through therapeutic intervention with IL10 and TGF-beta.
引用
收藏
页码:1577 / 1591
页数:15
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