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活体亲属及尸体移植中MLC刺激与移植物存活之间的相关性。

Correlation between MLC stimulation and graft survival in living related and cadaver transplants.

作者信息

Cochrum K C, Salvatierra O, Belzer F O

出版信息

Ann Surg. 1974 Oct;180(4):617-22. doi: 10.1097/00000658-197410000-00027.

Abstract

"Multiple MLC's" (parallel tests in recipient, donor and globulin-poor plasma) were performed in 211 consecutive transplant donor-recipient pairs(2) The two-way MLC's were performed on patients' lymphocytes before immunosuppression. All grafts regarded as "successful" were at risk for at least six months. Patients with a low MLC (Stimulation Index less than 8 times controls) usually had successful grafts (graft survival was 83% in related transplants and 76% in cadaver transplants). Patients with high MLC's had poor graft survival (0% graft survival in related transplants and 32% in cadaver transplants). An adjusted graft survival was calculated to exclude patients who died with normal renal function (serum creatinine less than 2 mg%). The adjusted graft survival was 91% for living related transplants and 88% for cadaver transplants. Falsely low MLC's occurred when the recipient's plasma contained low-titer cytotoxic antibodies. In 15 recipients of cadaver kidneys, the MLC in recipient plasma was significantly lower than MLC's in donor or globulin-poor plasma. Since the MLC when using cadaver donors was necessarily retrospective, the results were not known pre-transplant and all 15 grafts were rejected. In living related pairs, however, we were able to screen for such antibody activity and could avoid humoral presensitization and cellular compatibility.

摘要

对211例连续的移植供受者对进行了“多次混合淋巴细胞培养”(受者、供者及低球蛋白血浆中的平行试验)(2)。双向混合淋巴细胞培养在免疫抑制前对患者淋巴细胞进行。所有被视为“成功”的移植物至少有六个月处于风险中。混合淋巴细胞培养低(刺激指数低于对照8倍)的患者通常移植成功(亲属移植的移植物存活率为83%,尸体移植为76%)。混合淋巴细胞培养高的患者移植物存活率低(亲属移植的移植物存活率为0%,尸体移植为32%)。计算调整后的移植物存活率以排除肾功能正常(血清肌酐低于2mg%)死亡的患者。亲属活体移植的调整后移植物存活率为91%,尸体移植为88%。当受者血浆中含有低滴度细胞毒性抗体时会出现假性低混合淋巴细胞培养。在15例尸体肾受者中,受者血浆中的混合淋巴细胞培养显著低于供者或低球蛋白血浆中的混合淋巴细胞培养。由于使用尸体供者时混合淋巴细胞培养必然是回顾性的,移植前结果未知,所有15例移植物均被排斥。然而,在亲属活体配对中,我们能够筛查这种抗体活性,并且可以避免体液预致敏和细胞相容性问题。

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