Amada N, Okazaki H, Sato T, Ohashi Y, Kikuchi H
Sendai Shakaihoken Hospital, Sendai, Japan.
Transplant Proc. 2005 Mar;37(2):927-9. doi: 10.1016/j.transproceed.2004.12.289.
We examined whether deoxyspergualin (DSG) prophylaxis in combination with cyclosporine (CsA)- or tacrolimus (Tac)-based immunosuppression augments the effect of donor-specific blood transfusions (DSTs) to improve long-term survival of living-related renal-transplants.
From May 1985 to January 1998, 176 patients received DST from one-haplotype-identical donors prior to kidney transplantation. Group A (n = 64, 1985 to 1989) received CsA, prednisolone (PSL), antilymphocyte globulin (ALG), and azathioprine (AZA). Group B (n = 89, 1989 to 1996) received CsA, PSL, ALG, and DSG. Group C (n = 23, 1996 to 1998) received Tac, PSL, ALG, and DSG, with DSG followed by AZA. Rejection episodes were classified as acute rejection (AR, within the first 3 months) or late acute rejection (LAR, from 4 months to 1 year).
Five-year graft survivals were 73.4%, 88.8%, and 91.3% for groups A, B, and C, respectively. The incidence of AR was 34%, 30%, and 13%, and that of LAR was 23%, 26%, and 30% for groups A, B, and C, respectively. There was no significant difference in the incidence of AR or LAR among the three groups. However, an elevated serum creatinine (sCr) > or =1 mg/dL was observed in 73%, 15%, and 0% of patients during AR, and in 53%, 30%, and 14% during LAR for groups A, B, and C, respectively. These results suggest that the severity of AR or LAR was lowest among group C, contributing to the improved long-term graft survival in these patients.
DSG prophylaxis with Tac-based immunosuppression further improves long-term graft survival among living-related renal-transplant recipients treated with DST by decreasing the severity of acute rejection episodes.
我们研究了脱氧精胍菌素(DSG)预防联合基于环孢素(CsA)或他克莫司(Tac)的免疫抑制是否能增强供者特异性输血(DST)的效果,以提高亲属活体肾移植的长期存活率。
1985年5月至1998年1月,176例患者在肾移植前接受了来自单倍型相同供者的DST。A组(n = 64,1985年至1989年)接受CsA、泼尼松龙(PSL)、抗淋巴细胞球蛋白(ALG)和硫唑嘌呤(AZA)。B组(n = 89,1989年至1996年)接受CsA、PSL、ALG和DSG。C组(n = 23,1996年至1998年)接受Tac、PSL、ALG和DSG,DSG后使用AZA。排斥反应发作分为急性排斥(AR,在最初3个月内)或晚期急性排斥(LAR,4个月至1年)。
A、B、C三组的5年移植肾存活率分别为73.4%、88.8%和91.3%。A、B、C三组的AR发生率分别为34%、30%和13%,LAR发生率分别为23%、26%和30%。三组之间AR或LAR的发生率没有显著差异。然而,A、B、C三组在AR期间分别有73%、15%和0%的患者血清肌酐(sCr)升高≥1mg/dL,在LAR期间分别有53%、30%和14%的患者血清肌酐升高。这些结果表明,C组的AR或LAR严重程度最低,这有助于这些患者移植肾长期存活的改善。
通过降低急性排斥反应发作的严重程度,基于Tac的免疫抑制联合DSG预防可进一步提高接受DST的亲属活体肾移植受者的长期移植肾存活率。