Schachtner Thomas, Reinke Petra
Department of Nephrology and Internal Intensive Care, Charité University Medicine Berlin, Campus Virchow Clinic, Berlin, Germany.
Berlin-Brandenburg Center of Regenerative Therapies (BCRT), Berlin, Germany.
Transpl Infect Dis. 2016 Dec;18(6):881-888. doi: 10.1111/tid.12605. Epub 2016 Oct 21.
Because of the strikingly increased risk of post-transplant lymphoproliferative disorder (PTLD) in Epstein-Barr virus (EBV)-seronegative kidney transplant recipients (KTRs) from EBV-seropositive donors-EBV(D R ), special strategies need to be defined to prevent EBV transmission and EBV viremia.
We studied all KTRs at our center between 2008 and 2012. Seventeen of 402 KTRs (4.2%) were identified as EBV(D R ), among which 5 KTRs received kidneys from living donors and 12 KTRs from deceased donors. KTRs undergoing living donation were treated with a single dose of rituximab 4 weeks prior to transplantation. Assessment of EBV seroconversion and EBV viremia was performed.
Among 12 EBV-seronegative KTRs from deceased donors, all 12 KTRs (100%) showed EBV seroconversion, 7 KTRs (58%) showed active EBV viremia, and 1 KTR (8%) developed PTLD. In comparison, 3 of 5 KTRs from living donors, who received pretransplant rituximab, remained EBV-seronegative post transplantation, and no KTR developed EBV viremia (P<.05). All KTRs who received pretransplant rituximab showed excellent allograft function, with no increase in infections or malignancies.
Our data suggest that rituximab-mediated elimination of B cells may prevent transmission of EBV to the recipient, as EBV persistence requires the establishment of a latent infection in recipient B cells. Pretransplant rituximab may prove useful to prevent primary EBV infection in EBV-seronegative KTRs.
由于来自爱泼斯坦-巴尔病毒(EBV)血清学阳性供体的EBV血清学阴性肾移植受者(KTR)发生移植后淋巴细胞增生性疾病(PTLD)的风险显著增加,因此需要制定特殊策略来预防EBV传播和EBV病毒血症。
我们研究了2008年至2012年间本中心的所有KTR。402名KTR中有17名(4.2%)被确定为EBV(供受者血清学不匹配),其中5名KTR接受了活体供肾,12名KTR接受了尸体供肾。接受活体肾移植的KTR在移植前4周接受单剂量利妥昔单抗治疗。对EBV血清转化和EBV病毒血症进行了评估。
在12名接受尸体供肾的EBV血清学阴性KTR中,所有12名KTR(100%)均出现EBV血清转化,7名KTR(58%)出现活动性EBV病毒血症,1名KTR(8%)发生PTLD。相比之下,5名接受移植前利妥昔单抗治疗的活体供肾KTR中,有3名移植后仍为EBV血清学阴性,且没有KTR发生EBV病毒血症(P<0.05)。所有接受移植前利妥昔单抗治疗的KTR均显示出良好的移植肾功能,感染或恶性肿瘤均未增加。
我们的数据表明,利妥昔单抗介导的B细胞清除可能会阻止EBV传播给受者,因为EBV持续存在需要在受者B细胞中建立潜伏感染。移植前使用利妥昔单抗可能对预防EBV血清学阴性KTR的原发性EBV感染有用。