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首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >The association of lymphocytotoxic antibodies with corneal allograft rejection in high risk patients. The Collaborative Corneal Transplantation Studies Research Group.
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The association of lymphocytotoxic antibodies with corneal allograft rejection in high risk patients. The Collaborative Corneal Transplantation Studies Research Group.

机译:高危患者淋巴细胞毒性抗体与同种异体角膜排斥反应的关系。角膜移植研究小组。

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摘要

The Collaborative Corneal Transplantation Studies are a pair of multicenter prospective clinical trials evaluating the effectiveness of histocompatibility matching in high risk keratoplasty patients. The antigen matching study (AMS) evaluated HLA matching in patients without circulating lymphocytotoxic antibody to HLA antigens and the cross-match study (CS) evaluated the effect of using cross-match-negative donors in patients with identified circulating lymphocytotoxic antibodies to HLA antigens. Sera from 510 patients considered for enrollment in the studies were screened preoperatively for the presence of anti-class I lymphocytotoxic antibodies (LA). The 42 patients (8%) found to have detectable LA entered the CS. The 468 patients found not to have detectable LA preoperatively entered the AMS. Fifteen of the 37 transplanted CS patients were found to have donor-specific anti-class I antibody (before or after surgery). These patients were also screened for anti-class II LA and 25 had anti-class II panel reactive antibody > or = 5%. Forty-nine of the 419 transplanted AMS patients (12%) were found to have produced anti-class I LA after surgery, and in 19 patients, antibody specificities were those of donor HLA antigens. There was a significant association between the number of mismatched class I antigens and the number of donor-specific LA produced. The production of LA by AMS patients was significantly associated with reaction episodes; eighty-two percent of patients (40 of 49) with LA had reaction, compared with 63% of patients (230 of 365) without LA (P = 0.02). Likewise, production of donor-specific LA was significantly associated with immune-mediated graft failure (P = 0.025). For CS patients, there was no correlation between the production of donor-specific anti-class I or nonspecific anti-class II antibodies and graft outcome. However, the CS patients had poorer graft survival than did AMS patients at 3 years (57% vs. 66%, P = 0.01). These data demonstrate that LA, especially directed against donor class I HLA antigens following corneal transplantation in high risk patients, are associated with immune graft rejection and can be an indicator of allograft rejection.
机译:协作性角膜移植研究是一对评估高适应性角膜移植患者组织相容性匹配有效性的多中心前瞻性临床试验。抗原匹配研究(AMS)在没有针对HLA抗原的循环淋巴细胞毒性抗体的患者中评估HLA匹配,交叉匹配研究(CS)评估在已鉴定出针对HLA抗原的循环淋巴细胞毒性抗体的患者中使用交叉匹配阴性供体的效果。术前筛选了510名被纳入研究对象的患者的血清,以检查是否存在抗I类淋巴细胞毒性抗体(LA)。发现有可检测到的LA的42例患者(8%)进入CS。 468名术前未检测到LA的患者进入AMS。在37名移植的CS患者中,有15名(手术前后)具有供体特异性抗I类抗体。这些患者还接受了抗II类LA筛查,其中25例抗II类面板反应性抗体>或= 5%。在419名接受移植的AMS患者中,有49名(12%)在手术后产生了抗I LA,在19名患者中,抗体特异性与供体HLA抗原相同。错配的I类抗原数量与产生的供体特异性LA数量之间存在显着关联。 AMS患者产生的LA与反应发作显着相关。患有LA的患者中有82%(49名中的40名)有反应,而没有LA的患者中有63%(49名中的230名)有反应(P = 0.02)。同样,供体特异性LA的产生与免疫介导的移植失败密切相关(P = 0.025)。对于CS患者,供体特异性抗I类抗体或非特异性抗II类抗体的产生与移植结果之间没有相关性。但是,CS患者在3年时的移植物存活率比AMS患者低(57%对66%,P = 0.01)。这些数据表明,LA,特别是针对高危患者角膜移植后的I类HLA供体抗原,与免疫移植排斥反应有关,并且可以作为同种异体移植排斥反应的指标。

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