Speiser D E, Jeannet M
National Reference Laboratory for Histocompatibility and Swisstransplant, Hôpital Cantonal Universitaire de Genève, Switzerland.
Transpl Immunol. 1995 Dec;3(4):330-4. doi: 10.1016/0966-3274(95)80019-0.
Sensitized patients may reject renal transplants at a tempo or with a force dictated by their previous exposure to alloantigen. The patient's pretransplant alloimmunization status is usually assessed by the measurement of panel reactive antibodies (PRAs) and by the crossmatch. The test results using current patient's sera are of considerable predictive value. In contrast, the relevance of historical sera is much debated. To further investigate the correlation of PRA and crossmatch with clinical outcome, 852 cadaveric kidney transplants were evaluated. As expected, graft survival was significantly longer (p = 0.01;logrank test) in nonimmunized patients (n = 516) compared to immunized patients with more than 10% PRA (n = 297). Patients with persistently positive PRAs (n = 171) were then compared to patients with positive historical but negative current PRAs (n = 126). Interestingly, their graft survival was practically identical. Finally, transplants across a positive historical T cell crossmatch (n = 39) had a significantly reduced graft survival (p = 0.015) compared to transplants in immunized patients (n = 297, all T cell crossmatch negative). Thus, this study confirms the increased risk in sensitized patients and shows that the antigen specific immunological memory is of clinical relevance even if donor specific antibodies are not detectable in current sera.
致敏患者可能会根据其既往接触同种异体抗原的情况,以一定的速度或强度排斥肾移植。患者移植前的同种免疫状态通常通过检测群体反应性抗体(PRA)和交叉配型来评估。使用当前患者血清的检测结果具有相当大的预测价值。相比之下,既往血清结果的相关性则备受争议。为了进一步研究PRA和交叉配型与临床结局的相关性,对852例尸体肾移植进行了评估。正如预期的那样,与PRA超过10%的免疫患者(n = 297)相比,未免疫患者(n = 516)的移植物存活时间显著更长(p = 0.01;对数秩检验)。然后将PRA持续阳性的患者(n = 171)与既往PRA阳性但当前PRA阴性的患者(n = 126)进行比较。有趣的是,他们的移植物存活情况几乎相同。最后,与免疫患者(n = 297,所有T细胞交叉配型均为阴性)中的移植相比,既往T细胞交叉配型阳性的移植(n = 39)移植物存活显著降低(p = 0.015)。因此,本研究证实了致敏患者风险增加,并表明即使当前血清中检测不到供体特异性抗体,抗原特异性免疫记忆仍具有临床相关性。