Couvrat-Desvergnes Grégoire, Salama Apolline, Le Berre Ludmilla, Evanno Gwénaëlle, Viklicky Ondrej, Hruba Petra, Vesely Pavel, Guerif Pierrick, Dejoie Thomas, Rousse Juliette, Nicot Arnaud, Bach Jean-Marie, Ang Evelyn, Foucher Yohann, Brouard Sophie, Castagnet Stéphanie, Giral Magali, Harb Jean, Perreault Hélène, Charreau Béatrice, Lorent Marine, Soulillou Jean-Paul
J Clin Invest. 2015 Dec;125(12):4655-65. doi: 10.1172/JCI82267. Epub 2015 Nov 9.
Rabbit-generated antithymocyte globulins (ATGs), which target human T cells, are widely used as immunosuppressive agents during treatment of kidney allograft recipients. However, ATGs can induce immune complex diseases, including serum sickness disease (SSD). Rabbit and human IgGs have various antigenic differences, including expression of the sialic acid Neu5Gc and α-1-3-Gal (Gal), which are not synthesized by human beings. Moreover, anti-Neu5Gc antibodies have been shown to preexist and be elicited by immunization in human subjects. This study aimed to assess the effect of SSD on long-term kidney allograft outcome and to compare the immunization status of grafted patients presenting with SSD following ATG induction treatment.
We analyzed data from a cohort of 889 first kidney graft recipients with ATG induction (86 with SSD [SSD(+)] and 803 without SSD [SSD(-)]) from the Données Informatisées et Validées en Transplantation data bank. Two subgroups of SSD(+) and SSD(-) patients that had received ATG induction treatment were then assessed for total anti-ATG, anti-Neu5Gc, and anti-Gal antibodies using ELISA assays on sera before and after transplantation.
SSD was significantly associated with long-term graft loss (>10 years, P = 0.02). Moreover, SSD(+) patients exhibited significantly elevated titers of anti-ATG (P = 0.043) and anti-Neu5Gc (P = 0.007) IgGs in late post-graft samples compared with SSD(-) recipients.
In conclusion, our data indicate that SSD is a major contributing factor of late graft loss following ATG induction and that anti-Neu5Gc antibodies increase over time in SSD(+) patients.
This study was funded by Société d'Accélération du Transfert de Technologies Ouest Valorisation, the European FP7 "Translink" research program, the French National Agency of Research, Labex Transplantex, the Natural Science and Engineering Research Council of Canada, and the Canadian Foundation for Innovation.
兔源性抗胸腺细胞球蛋白(ATG)可靶向人类T细胞,在肾移植受者治疗期间被广泛用作免疫抑制剂。然而,ATG可诱发免疫复合物疾病,包括血清病(SSD)。兔和人IgG存在多种抗原差异,包括唾液酸Neu5Gc和α-1-3-半乳糖(Gal)的表达,而人类无法合成这些物质。此外,抗Neu5Gc抗体已被证明在人类受试者中预先存在且可通过免疫激发产生。本研究旨在评估SSD对肾移植长期预后的影响,并比较接受ATG诱导治疗后出现SSD的移植患者的免疫状态。
我们分析了来自移植信息数据库的889例接受ATG诱导的首次肾移植受者队列的数据(86例患有SSD [SSD(+)],803例未患SSD [SSD(-)])。然后,使用ELISA法对接受ATG诱导治疗的SSD(+)和SSD(-)患者的两个亚组在移植前后的血清中的总抗ATG、抗Neu5Gc和抗Gal抗体进行评估。
SSD与长期移植失败显著相关(>10年,P = 0.02)。此外,与SSD(-)受者相比,SSD(+)患者在移植后期样本中的抗ATG(P = 0.043)和抗Neu5Gc(P = 0.007)IgG滴度显著升高。
总之,我们的数据表明,SSD是ATG诱导后移植后期失败的主要促成因素,并且抗Neu5Gc抗体在SSD(+)患者中随时间增加。
本研究由法国西部技术转移加速协会、欧洲FP7“Translink”研究计划、法国国家研究机构、Labex Transplantex、加拿大自然科学与工程研究理事会以及加拿大创新基金会资助。