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肾移植患者输注供体骨髓的六年临床疗效

Six-year clinical effect of donor bone marrow infusions in renal transplant patients.

作者信息

Ciancio G, Miller J, Garcia-Morales R O, Carreno M, Burke G W, Roth D, Kupin W, Tzakis A G, Ricordi C, Rosen A, Fuller L, Esquenazi V

机构信息

Department of Surgery, Diabetes Research Institute, University of Miami School of Medicine, Florida 33101, USA.

出版信息

Transplantation. 2001 Apr 15;71(7):827-35. doi: 10.1097/00007890-200104150-00002.

Abstract

BACKGROUND

To date, several single- and multicenter clinical trials have attempted to induce specific immunological unresponsiveness using donor bone marrow cell infusions to augment solid organ transplantation, but the outcomes have not been definitive.

METHODS

Between September 1994 and May 1998, 63 cadaver (CAD) renal transplant recipients of either one or two postoperative donor bone marrow cell (DBMC) infusions were prospectively compared with 219 non-infused controls given equivalent immunosuppression. There was at least a 1 HLA DR antigen match present between donors and recipients. The immunosuppressive regimen included a 10-day course of OKT3 induction, and tacrolimus, mycophenolate mofetil, and methylprednisolone maintenance. A total 7.01x10(8)+/-1.9x10(8) (SD) DBMC/kg was infused into the CAD recipients on either days 4 and 11 (n=42) or one half of that dose on day 4 (n=21) postoperatively. Clinical follow-up has ranged from 2.9 to 6.3 years (mean, 4.7 years). Studies were also performed of humoral immunity and quantitative cellular chimerism.

RESULTS

There is clear-cut equivalence in immunosuppressive dosaging and in the other major demographic variables in both groups. However, only 2/63 DBMC recipients had biopsy-proven chronic rejection, whereas 41/219 showed chronic rejection in the controls (P = <0.01). In both groups, mortality was not associated with rejection. The actuarial graft survival at 6.3 years in the CAD DBMC group was 84.3% compared with 72.2% in the control group (not statistically significant). However, if death with a functioning graft was excluded, graft survival was 94.1% in the DBMC group and 79.8% in the controls (P=0.039). Forty patients in the control group continue to have deteriorating renal function (increasing serum creatinine concentrations to 2 mg/dl and higher), compared with 2 patients in the DBMC group (P=0.04). In the DBMC group, chimerism in iliac crest marrow aspirates has increased 3-fold in yearly sequential measurements between 1 and 4 years postoperatively averaging 1.3+/-0.36% (SE) most recently. This has not occurred in the controls.

CONCLUSIONS

There now appears to be more solid long-term evidence, in kidney transplant recipients prospectively receiving DBMC infusions, of an improvement in long-term graft survival, and of the degree of chimerism positively correlating with the absence of graft loss.

摘要

背景

迄今为止,多项单中心和多中心临床试验试图通过输注供体骨髓细胞来诱导特异性免疫无反应,以促进实体器官移植,但结果尚无定论。

方法

1994年9月至1998年5月,对63例接受一或两次术后供体骨髓细胞(DBMC)输注的尸体肾移植受者进行前瞻性研究,并与219例接受同等免疫抑制但未输注的对照组进行比较。供体与受者之间至少有1个HLA DR抗原匹配。免疫抑制方案包括10天的OKT3诱导疗程,以及他克莫司、霉酚酸酯和甲泼尼龙维持治疗。将总量为7.01x10(8)+/-1.9x10(8)(标准差)个DBMC/kg于术后第4天和第11天(n = 42)或仅在第4天输注一半剂量(n = 21)给尸体肾移植受者。临床随访时间为2.9至6.3年(平均4.7年)。还进行了体液免疫和定量细胞嵌合研究。

结果

两组在免疫抑制剂量和其他主要人口统计学变量方面明显相当。然而,仅2/63例DBMC受者经活检证实有慢性排斥反应,而对照组中有41/219例出现慢性排斥反应(P = <0.01)。两组的死亡率均与排斥反应无关。尸体肾移植DBMC组6.3年时的实际移植存活率为84.3%,而对照组为72.2%(无统计学意义)。然而,若排除移植肾仍有功能时的死亡病例,则DBMC组的移植存活率为94.1%,对照组为79.8%(P = 0.039)。对照组中有40例患者肾功能持续恶化(血清肌酐浓度升至2mg/dl及更高),而DBMC组仅有2例(P = 0.04)。在DBMC组,术后1至4年每年连续测量显示,髂嵴骨髓穿刺物中的嵌合率增加了3倍,最近平均为1.3+/-0.36%(标准误)。对照组未出现这种情况。

结论

对于前瞻性接受DBMC输注的肾移植受者,目前似乎有更确凿的长期证据表明长期移植存活率有所提高,且嵌合程度与移植肾无丢失呈正相关。

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