[The efficacy and safety of protein A immunoadsorption combined with rituximab treatment for highly sensitized patients undergoing haplo-hematopoietic stem cell transplantation].

L Li, W J Zhu, Q Zhu, S Y Zhou, C Ma, J Wang, X H Hu, Y Han, Y Wang, X W Tang, X Ma, S N Chen, H Y Qiu, L Y Chen, J He, D P Wu, X J Wu
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引用次数: 0

Abstract

Objective: To investigate the efficacy and safety of protein A immunoadsorption (PAIA) combined with rituximab (RTX) in highly sensitized patients who underwent haplo-hematopoietic stem cell transplantation (haplo-HSCT) . Methods: The clinical data of 56 highly sensitized patients treated with PAIA and RTX before haplo-HSCT at the First Affiliated Hospital of Soochow University and Soochow Hopes Hematonosis Hospital between March 2021 and June 2023 were retrospectively analyzed. The number of human leukocyte antigen (HLA) antibody types and the mean fluorescence intensity (MFI), humoral immunity, adverse reactions during adsorption, and survival within 100 days before and after adsorption were measured. Results: After receiving the PAIA treatment, the median MFI of patients containing only HLA Ⅰ antibodies decreased from 7 859 (3 209-12 444) to 3 719 (0-8 275) (P<0.001), and the median MFI of HLA Ⅰ+Ⅱ antibodies decreased from 5 476 (1 977-12 382) to 3 714 (0-11 074) (P=0.035). The median MFI of patients with positive anti-donor-specific antibodies decreased from 8 779 (2 697-18 659) to 4 524 (0-15 989) (P<0.001). The number of HLA-A, B, C, DR, and DQ antibodies in all patients decreased after the PAIA treatment, and the differences were statistically significant (A, B, C, DR: P<0.001, DQ: P<0.01). The humoral immune monitoring before and after the PAIA treatment showed a significant decrease in the number of IgG and complement C3 (P<0.001 and P=0.002, respectively). Forty-four patients underwent HLA antibody monitoring after transplantation, and the overall MFI and number of antibody types decreased. However, five patients developed new antibodies with low MFI, and nine patients continued to have high MFI. The overall survival, disease-free survival, non-recurrent mortality, and cumulative recurrence rates at 100 days post-transplantation were 83.8%, 80.2%, 16.1%, and 4.5%, respectively. Conclusions: The combination of PAIA and RTX has a certain therapeutic effect and good safety in the desensitization treatment of highly sensitive patients before haplo-HSCT.

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[蛋白 A 免疫吸附联合利妥昔单抗治疗接受单倍体造血干细胞移植的高度致敏患者的有效性和安全性]。
目的研究蛋白 A 免疫吸附(PAIA)联合利妥昔单抗(RTX)对接受单倍体造血干细胞移植(haplo-HSCT)的高度致敏患者的有效性和安全性。方法:回顾性分析2021年3月至2023年6月期间在苏州大学附属第一医院和苏州霍普斯血液病医院接受PAIA和RTX治疗的56例高度致敏患者的临床数据。测量人类白细胞抗原(HLA)抗体类型数量和平均荧光强度(MFI)、体液免疫、吸附过程中的不良反应以及吸附前后100天内的存活率。结果显示接受 PAIA 治疗后,仅含有 HLA Ⅰ 型抗体的患者的中位 MFI 从 7 859(3 209-12 444)降至 3 719(0-8 275)(PP=0.035)。抗供体特异性抗体阳性患者的中位 MFI 从 8 779(2 697-18 659)降至 4 524(0-15 989)(PPPPP分别=0.002)。44 名患者在移植后接受了 HLA 抗体监测,总体 MFI 和抗体类型数量均有所下降。然而,有五名患者出现了新的低MFI抗体,九名患者的MFI仍然很高。移植后100天的总生存率、无病生存率、非复发死亡率和累积复发率分别为83.8%、80.2%、16.1%和4.5%。结论PAIA和RTX联合应用于单倍体造血干细胞移植前高度敏感患者的脱敏治疗具有一定的疗效和良好的安全性。
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