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Toll-like 4 receptor (TLR4) expression on peripheral blood mononuclear cells in renal transplant recipients with pre-transplant chronic interstitial nephritis indicates patients at risk of graft deterioration
被引:1
|作者:
Zmonarski, Slawomir C.
[1
]
Banasik, Miroslaw
[1
]
Golebiowski, Tomasz
[1
]
Madziarska, Katarzyna
[1
]
Mazanowska, Oktawia
[1
]
Myszka, Marta
[1
]
Zmonarska, Joanna
[2
]
Letachowicz, Krzysztof
[1
]
Dawiskiba, Tomasz
[3
]
Krajewska, Magdalena
[1
]
机构:
[1] Wroclaw Med Univ, Dept Nephrol & Transplantat Med, Borowska 213 Str, PL-50553 Wroclaw, Poland
[2] Wroclaw Med Univ, Fac Med, Wyb Ludwika Pasteura 1, PL-50367 Wroclaw, Poland
[3] Wroclaw Med Univ, Dept Vasc Gen & Transplant Surg, Borowska 213 Str, PL-50553 Wroclaw, Poland
关键词:
Chronic interstitial nephritis;
Pyelonephritis;
Toll-like;
4;
receptor;
Transplanted kidney;
Tacrolimus;
Cyclosporine-A;
URINARY-TRACT-INFECTION;
ACUTE PYELONEPHRITIS;
INNATE IMMUNITY;
KIDNEY;
REJECTION;
SURVIVAL;
POLYMORPHISMS;
MACROPHAGES;
MONOCYTES;
D O I:
10.1016/j.trim.2020.101319
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Data binding the expression of Toll-like 4 receptor (TLR4ex), transplanted kidney function, and the cause of pretransplant end-stage renal disease are scarcely available. Objective: To investigate the relationship between pre-transplant chronic interstitial nephritis (CIN), TLR4ex and transplanted kidney function. Materials and methods: TLR4ex was measured in peripheral blood mononuclear cells of 43 CIN kidney transplant recipients. We compared TLR4ex among 33 patients with pre-transplant chronic non-infectious interstitial nephritis (NIN) and 10 patients with pre-transplant chronic pyelonephritis (Py). At the beginning (Day-0) TLR4ex, as well as concentrations of cyclosporin A (CyA) and tacrolimus (TAC) were determined. Both CIN and NIN patients were divided according to the respective median of TLR4ex into groups of low-TLR4 expression (L-TLR4ex) and high-TLR4 expression (H-TLR4ex). Serum creatinine/glomerular filtration rate (sCr/EGFR) was assessed on Day-0 and after the follow-up (F-up). The magnitudes of sCr/EGFR change (Delta sCr/Delta EGFR) were evaluated. The treatment was maintained stable along the F-up period (median 11.9 months). Results: Day-0: in CIN with L-TLR4ex TAC was lower but sCr/EGFR were not different from H-TLR4ex; in Py TLR4ex and TAC were lower than in NIN with no difference in sCR/eGFR. After F-up: in CIN with L-TLR4ex sCR/EGFR and Delta sCr/Delta EGFR were worse than in H-TLR4ex; in Py sCR/EGFR and Delta sCr/Delta EGFR were worse than in NIN. The regression analysis points out prospective impact of Py and TLR4ex on sCR/eGFR and Delta sCr/Delta eGFR. Conclusion: In CIN, both TLR4ex and Tac appear to be a useful positive predictor of the effectiveness of immunosuppression. Chronic pyelonephritis indirectly promotes faster progression of chronic transplanted kidney disease.
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