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肾移植受者中新型供者特异性 HLA 抗体的产生与外周 CD4(+)CD25(高)细胞:存在相互作用的空间?

De Novo Donor-Specific HLA Antibody Development and Peripheral CD4(+)CD25(high) Cells in Kidney Transplant Recipients: A Place for Interaction?

作者信息

Alberu Josefina, Vargas-Rojas Maria Inés, Morales-Buenrostro Luis E, Crispin Jose C, Rodríguez-Romo Roxana, Uribe-Uribe Norma O, Carrasco Gabriel, Gómez-Martín Diana, Alcocer-Varela Jorge

机构信息

Department of Transplantation, National Institute of Medical Science and Nutrition Salvador Zubirán, Vasco de Quiroga 15, Colonia Sección XVI, DF, 14000 Mexico City, Mexico.

出版信息

J Transplant. 2012;2012:302539. doi: 10.1155/2012/302539. Epub 2012 Aug 23.

Abstract

The aim of this study was to determine whether the abundance of regulatory T cells (Tregs) (CD4(+)CD25(high)) affects the de novo development of anti-HLA donor-specific antibodies (DSAs) in kidney transplant recipients (KTRs). Methods. Unsensitized (PRA ≤ 10%, no DSA) adult primary KTRs who received a living (83%) or deceased (17%) KT in our Institution during 2004/2005 were included. DSA testing was performed monthly, and Tregs were quantified by flow cytometry every 3 months, during the 1st year after KT. All patients received triple drug immunosuppressive therapy (CNI + MMF or AZA + PDN); 83% received anti-CD25. Results. 53 KTRs were included; 32% developed DSA during the 1st year after KT. Significantly lower 7-year graft survival was observed in those who developed DSA. No difference was observed in Treg numbers up to 9 months after KT, between DSA positive and negative. However, at 12 months after KT, DSA-negative patients had significantly higher numbers of Treg. Conclusions. Early development of DSA was not associated to variations in Treg abundance. The differences in Treg numbers observed at the late time point may reflect better immune acceptance of the graft and may be associated to long-term effects. Additional inhibitory mechanisms participating earlier in DSA development after KT deserve to be sought.

摘要

本研究的目的是确定调节性T细胞(Tregs,CD4(+)CD25(high))的丰度是否会影响肾移植受者(KTRs)中抗HLA供体特异性抗体(DSAs)的从头产生。方法。纳入2004/2005年期间在本机构接受活体(83%)或尸体(17%)肾移植的未致敏(PRA≤10%,无DSA)成年原发性KTRs。肾移植术后第1年,每月进行DSA检测,每3个月通过流式细胞术对Tregs进行定量。所有患者均接受三联药物免疫抑制治疗(CNI + MMF或AZA + PDN);83%接受抗CD25治疗。结果。纳入53例KTRs;32%在肾移植术后第1年出现DSA。出现DSA的患者7年移植物存活率显著降低。肾移植术后9个月内,DSA阳性和阴性患者的Treg数量无差异。然而,肾移植术后12个月,DSA阴性患者的Treg数量显著更高。结论。DSA的早期产生与Treg丰度的变化无关。在后期观察到的Treg数量差异可能反映了对移植物更好的免疫接受,并且可能与长期影响有关。值得寻找在肾移植术后DSA产生早期参与的其他抑制机制。

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