Lin Thomas S, Zahrieh David, Weller Edie, Alyea Edwin P, Antin Joseph H, Soiffer Robert J
Department of Adult Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts, USA.
Transplantation. 2002 Jul 15;74(1):49-54. doi: 10.1097/00007890-200207150-00009.
Cytomegalovirus (CMV) infection is a significant cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (HSCT). Recipients of T-cell-depleted (TCD) transplants may be more susceptible to CMV infection as a result of the reduction in transferred T cell immunity. We sought to determine the effect of prior donor and patient CMV exposure on the incidence of CMV infection after TCD allogeneic HSCT.
We retrospectively examined CMV antigen testing results in all patients who had undergone CD6+ TCD related and unrelated donor allogeneic HSCT at our institution from 1996 to 1999. All 124 patients who had documented donor and recipient CMV serologies pretransplant and had undergone CMV antigen testing before day +100 posttransplant were included in the analysis.
Forty-one percent of seropositive recipients and 1% of seronegative recipients developed evidence of CMV reactivation (odds ratio 54.1, 95% confidence interval [CI] 6.9-424.1, P<0.001). Prior donor CMV exposure did not place seronegative recipients at increased risk of CMV conversion. Multivariable analysis indicated that prior donor CMV exposure significantly reduced the risk of CMV reactivation in seropositive recipients by 81% (odds ratio 0.19, 95% CI 0.04-0.91, P=0.04). Grades II to IV acute graft-versus-host disease (GVHD) was associated with CMV conversion (P=0.04) when seropositive recipients underwent HSCT from CMV-negative donors, but not when the donor was CMV-seropositive (P=0.54).
The CMV serology status of the recipient, rather than the donor, was the primary determinant of risk for CMV conversion after TCD allogeneic HSCT. Despite CD6+ T-cell depletion, immunity against CMV seemed to be transferred with the donor graft and protected seropositive HSCT recipients from CMV reactivation.
巨细胞病毒(CMV)感染是异基因造血干细胞移植(HSCT)后发病和死亡的重要原因。由于移植的T细胞免疫功能降低,T细胞去除(TCD)移植受者可能更容易感染CMV。我们试图确定供体和患者既往CMV暴露对TCD异基因HSCT后CMV感染发生率的影响。
我们回顾性检查了1996年至1999年在我们机构接受CD6 + TCD相关和无关供体异基因HSCT的所有患者的CMV抗原检测结果。分析纳入了所有124例在移植前有记录的供体和受者CMV血清学检查结果且在移植后+100天之前接受过CMV抗原检测的患者。
41%的血清阳性受者和1%的血清阴性受者出现CMV重新激活的证据(优势比54.1,95%置信区间[CI] 6.9 - 424.1,P < 0.001)。既往供体CMV暴露并未使血清阴性受者发生CMV转化的风险增加。多变量分析表明,既往供体CMV暴露使血清阳性受者CMV重新激活的风险显著降低81%(优势比0.19,95% CI 0.04 - 0.91,P = 0.04)。当血清阳性受者接受来自CMV阴性供体的HSCT时,II至IV级急性移植物抗宿主病(GVHD)与CMV转化相关(P = 0.04),但当供体为CMV血清阳性时则无相关性(P = 0.54)。
TCD异基因HSCT后CMV转化风险的主要决定因素是受者而非供体的CMV血清学状态。尽管进行了CD6 + T细胞去除,但针对CMV的免疫似乎随供体移植物转移,并保护血清阳性HSCT受者免于CMV重新激活。