Leffell M S, Cao K, Coppage M, Hansen J A, Hart J M, Pereira N, Pereira S, Reinsmoen N L, Senitzer D, Smith A, Torres M, Vega R, Fuchs E
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Tissue Antigens. 2009 Dec;74(6):494-8. doi: 10.1111/j.1399-0039.2009.01377.x. Epub 2009 Oct 4.
As part of the 15th International Histocompatibility and Immunogenetics Workshop (IHIWS), seven centers participated in a collaborative project to determine whether any significant humoral sensitization occurred post-transplant among recipients of HLA partially mismatched hematopoietic cell transplants (HCTs). A total of 140 donor/recipient pairs were enrolled with a total of 367 pre-and post-transplant sera analyzed. The majority of the samples (69.1%) were obtained within 30-90 days post-HCT. HLA-specific antibodies were defined using single antigen bead assays on a Luminex platform with a positive cutoff value of 1000 normalized median fluorescence intensity (MFI). There was an overall incidence of post-HCT sensitization toward donor HLA mismatches of 5.7%; however, all cases were among recipients of one HLA haplotype-mismatched grafts under nonmyeloablative, pre-transplant conditioning. Among the one haplotype-mismatched recipients, 15.7% (8/51) developed donor HLA-specific antibodies and 29.4% also had antibodies directed toward third party HLA antigens. Among the donor-specific antibodies, 9.8% were directed toward HLA class I antigens; 7.8% were against class II antigens; and 2.0% had both class I and II specificity. The relative strength of post-transplant antibodies was low with no significant difference in the mean maximum MFI values between third party and donor-specific antibodies. Because only a small number (10.2%) of the post-transplant samples were obtained 180 days or more post-HCT, longer term study is needed to evaluate any clinical relevance of these low-to-moderate levels of donor-specific antibody in one haplotype-mismatched recipients, as well as to determine whether any other antibodies occur at later times.
作为第15届国际组织相容性与免疫遗传学研讨会(IHIWS)的一部分,七个中心参与了一个合作项目,以确定在HLA部分错配的造血细胞移植(HCT)受者中,移植后是否发生了任何显著的体液致敏。共纳入了140对供体/受体对,共分析了367份移植前和移植后的血清。大多数样本(69.1%)是在HCT后30 - 90天内获得的。使用Luminex平台上的单抗原珠试验定义HLA特异性抗体,阳性截断值为1000标准化中位荧光强度(MFI)。HCT后对供体HLA错配的致敏总体发生率为5.7%;然而,所有病例均为接受非清髓性移植前预处理的一个HLA单倍型错配移植物的受者。在单倍型错配的受者中,15.7%(8/51)产生了供体HLA特异性抗体,29.4%还具有针对第三方HLA抗原的抗体。在供体特异性抗体中,9.8%针对HLA I类抗原;7.8%针对II类抗原;2.0%同时具有I类和II类特异性。移植后抗体的相对强度较低,第三方抗体和供体特异性抗体的平均最大MFI值之间无显著差异。由于仅10.2%的移植后样本是在HCT后180天或更长时间获得的,因此需要进行长期研究,以评估这些低至中等水平的供体特异性抗体在单倍型错配受者中的任何临床相关性,以及确定是否在更晚的时间出现任何其他抗体。