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Effect of Donor Cell Type on Complement-Dependent Cytotoxicity Crossmatch Outcome for Patients Immunized Against HLA Class-II Antigens

机译:供体细胞类型对免疫HLA II类抗原的患者补体依赖性细胞毒性交叉匹配结果的影响

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Objectives: In the Eurotransplant zone, the crossmatch serum exchange program was established to reduce unnecessary organ shipment, using the complement-dependent cytotoxicity crossmatch as the reference to make the decision. Crossmatching at the donor center dictates whether the transplant should be shipped to the recipient center where a decisive crossmatch would then be done. However, in recent years, the target cell used for the crossmatching has changed from spleen cells to peripheral blood lymphocytes. In this study, we assess the impact of this change on the outcome of complement-dependent cytotoxicity crossmatches for patients immunized against HLA-class II. Materials and Methods: The influence of the donor cell type was analyzed by crossmatching unseparated peripheral blood lymphocytes, separated T and B lymphocytes, as well as spleen cells from 12 organ donors with sera from 40 immunized kidney retransplant candidates. Negative sera and sera harboring only anti-HLA class-II antibodies were used as additional controls.We did more than 1200 complement-dependent cytotoxicity crossmatches. Results: Crossmatches with sera containing anti-HLA class-I plus class-II alloantibodies (n=113 per cell type) were positive in 42% of peripheral blood lymphocytes, 72% of spleen cells, and 81% of B cells. Crossmatches with sera containing exclusively anti-HLA class-II antibodies (n=89 per cell type) were positive in 1% of peripheral blood lymphocytes, 30% of spleen cells, and in 31% of B cells. Overall, spleen or separated B cells identified approximately 30% more positive donor-recipient pairs. Conclusions: The data show that the change from spleen cells to peripheral blood lymphocytes as donor target cells for complement-dependent cytotoxicity crossmatching increased risk of false negative results for patients harboring anti-HLA class-II antibodies.
机译:目的:在欧洲移植区,建立了交叉配比血清交换程序,以减少不必要的器官运输,并以补体依赖性细胞毒性交叉配比为决策依据。供体中心的交叉匹配决定了是否应将移植物运送到接受者中心,然后再进行决定性的交叉匹配。然而,近年来,用于交叉匹配的靶细胞已经从脾细胞变为外周血淋巴细胞。在这项研究中,我们评估了这种变化对II类HLA免疫患者补体依赖性细胞毒性交叉匹配结果的影响。材料和方法:通过交叉匹配未分离的外周血淋巴细胞,分离的T和B淋巴细胞,以及来自12个器官供体的脾细胞与40个经免疫的肾脏移植候选者的血清,来分析供体细胞类型的影响。阴性血清和仅包含抗HLA II类抗体的血清用作其他对照。我们进行了1200多次依赖补体的细胞毒性交叉配对。结果:与含有抗HLA I类和II类同种抗体的血清(每个细胞类型n = 113)的交叉匹配在42%的外周血淋巴细胞,72%的脾细胞和81%的B细胞中为阳性。与仅含有抗HLA II类抗体的血清的交叉匹配(每种细胞类型n = 89)在1%的外周血淋巴细胞,30%的脾细胞和31%的B细胞中为阳性。总体而言,脾脏或分离的B细胞可鉴定出约30%的阳性供体-受体对。结论:数据表明,从脾细胞到外周血淋巴细胞作为补体依赖性细胞毒性交叉匹配供体靶细胞的变化,增加了携带抗HLA II类抗体的患者假阴性结果的风险。

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