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DOI 10.1016/j.intimp.2019.105803

Медицинская библиотека · International immunopharmacology · 2019

Assessment of serum Tim-3 and Gal-9 levels in predicting the risk of infection after kidney transplantation.

Li Ya Mei, Li Yi, Yan Lin, Tang Jiang Tao, Wu Xiao Juan, Bai Yang Juan, An Yun Fei, Dai Bo, Yang Cui Li, Wang Lan Lan, Shi Yun Ying

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Аннотация

Infection remains a major cause of morbidity and mortality after kidney transplantation (KT). Reliable biomarkers to predict post-transplant infection are lacking. We investigated the predictive performance of pre- and post-transplant levels of T-cell immunoglobulin and mucin domain-3 (Tim-3) and Galectin-9 (Gal-9), two pleiotropic immunomodulatory molecules, in early identification of infection. Serum Tim-3 and Gal-9 were paired measured before and 30 days after transplantation (PTD 30) in 95 KT recipients (KTRs). The decline rates of Tim-3 and Gal-9 were calculated relative to pre-transplant levels. KTRs with infection history had significantly higher levels of PTD 30 Tim-3 and Gal-9, and slower decrease rates of Gal-9 compared to non-infected recipients, while no difference was observed between two groups regarding pre-transplant levels. The AUCs for predicting 1-year post-transplant infection were 0.653 and 0.711 for post-transplant Tim-3 and Gal-9, 0.664 and 0.670 for relative Tim-3 and Gal-9, respectively. After adjusting for potential confounders, PTD 30 Tim-3, Gal-9 and relative Gal-9 remained as independent risk factors for post-transplant infection. Our results suggested that PTD 30 Tim-3 and Gal-9 and relative decrease of Gal-9 were promising predictors for identifying KTRs with high risk of infection, while pre-transplant Tim-3 and Gal-9 showed no predictive power to infection.

Для цитирования: Li Ya Mei, Li Yi, Yan Lin, Tang Jiang Tao, Wu Xiao Juan, Bai Yang Juan, An Yun Fei, Dai Bo, Yang Cui Li, Wang Lan Lan, Shi Yun Ying. Assessment of serum Tim-3 and Gal-9 levels in predicting the risk of infection after kidney transplantation.. International immunopharmacology. 2019. DOI: 10.1016/j.intimp.2019.105803.

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