Division of Nephrology, Department of Medicine, University of Wisconsin School of Medicine and Public Health, Madison, WI.
Division of Transplant Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI.
Transplantation. 2019 Feb;103(2):435-440. doi: 10.1097/TP.0000000000002339.
Development of de novo donor-specific antibodies (dnDSA) has detrimental effects on graft survival in several types of solid organ transplants. However, limited information exists about the effect of dnDSA on pancreas transplant graft survival.
We report our experience with pancreas recipients transplanted between January 01, 2005, and August 31, 2017.
We identified 541 pancreas transplant recipients, of which 121 developed dnDSA and 420 did not. Thirty-two percent developed dnDSA against HLA class I antigens, 56% developed against class II antigens, and 12% developed against both. Fifty-two percent of the patients in the dnDSA+ and 24% in the dnDSA- group underwent pancreas biopsy, mainly due to a rise in pancreatic enzymes. Rejection was found in 42% of the dnDSA+ group, and 20% of the dnDSA- group(P < 0.001). There were 36% uncensored graft failures in the dnDSA+ group and 17% uncensored failures in the dnDSA- group (P < 0.001). A similar trend was seen in death-censored graft failure between the groups. In univariate Cox regression analyses, male sex, older age, and recipients of simultaneous pancreas and kidney transplant were found to be protective for death-censored graft failure; multiple transplants, dnDSA, requirement for pancreas biopsy and presence of pancreas rejection were associated with increased risk of graft failure. In multivariate analysis, only older age and dnDSA were significantly associated with death-censored graft failure.
Our findings suggest that dnDSA in pancreas transplant recipients are associated with increased rates of rejection and graft failure. Timely detection of dnDSA through regular screening and early treatment of pancreas rejection may ultimately improve graft outcomes.
在几种实体器官移植中,新产生的供体特异性抗体(dnDSA)的发展对移植物的存活有不利影响。然而,关于 dnDSA 对胰腺移植移植物存活的影响的信息有限。
我们报告了 2005 年 1 月 1 日至 2017 年 8 月 31 日期间接受胰腺移植的患者的经验。
我们确定了 541 名胰腺移植受者,其中 121 名产生了 dnDSA,420 名未产生 dnDSA。32%的患者产生针对 HLA Ⅰ类抗原的 dnDSA,56%的患者产生针对Ⅱ类抗原的 dnDSA,12%的患者产生针对两者的 dnDSA。dnDSA+组中 52%的患者和 dnDSA-组中 24%的患者进行了胰腺活检,主要是由于胰腺酶升高。dnDSA+组中发现 42%的排斥反应,dnDSA-组中发现 20%(P<0.001)。dnDSA+组中有 36%的无删失移植物失败,dnDSA-组中有 17%的无删失移植物失败(P<0.001)。两组间死亡删失移植物失败也有类似的趋势。在单变量 Cox 回归分析中,男性、年龄较大和同时接受胰腺和肾脏移植的受者被发现对死亡删失移植物失败具有保护作用;多次移植、dnDSA、胰腺活检的需要和胰腺排斥的存在与移植物失败的风险增加相关。在多变量分析中,只有年龄较大和 dnDSA 与死亡删失移植物失败显著相关。
我们的研究结果表明,胰腺移植受者中的 dnDSA 与排斥反应和移植物失败的发生率增加有关。通过定期筛查及时发现 dnDSA,并早期治疗胰腺排斥反应,最终可能改善移植物结局。