Cowan M J, Wara D W, Weintrub P S, Pabst H, Ammann A J
J Clin Immunol. 1985 Nov;5(6):370-6. doi: 10.1007/BF00915333.
The major limitation of mismatched bone marrow transplantation is fatal graft versus host disease (GVHD). We processed haplotype-identical parental marrow with soybean agglutinin (SBA), sheep erythrocytes (SRBC), and neuraminidase-treated SRBC (N-SRBC) to enrich for marrow stem cells and remove mature T cells. Nine patients with severe combined immunodeficiency disease (SCID) who lacked histocompatible donors received these SBA-negative, SRBC-negative, N-SRBC-negative marrow transplants (0.5-5.0 X 10(8) cells/kg). Seven of the nine patients (78%) had documented T-lymphocyte engraftment based on HLA typing and/or chromosomal analysis. Six patients showed evidence of B-cell immunity on the basis of increased immunoglobulin levels, isohemagglutinins, and/or HLA-DR typing of non-T cells. Three patients received marrow ablative chemotherapy pretransplant for maternal-fetal GVHD; neutrophil engraftment occurred between 9 and 17 days posttransplantation, erythrocytes engrafted within 3-4 weeks of transplantation, and platelet recovery was seen between day 17 and day 49 following the transplants. No immunosuppression was given prophylactically posttransplant. Three patients had no GVHD, two had transient rash and/or fever, and two developed mild focal (stage I) chronic cutaneous GVHD. Of the seven who engrafted, five (71%) are alive and clinically well without GVHD 18-35 months posttransplant. These data demonstrate that SBA- and SRBC/N-SRBC-treated haploidentical marrow transplantation results in functional lymphocyte engraftment in SCID without significant GVHD, and can be used for some patients who otherwise would have no hope for survival.
不相匹配的骨髓移植的主要局限性是致命的移植物抗宿主病(GVHD)。我们用大豆凝集素(SBA)、绵羊红细胞(SRBC)和神经氨酸酶处理的SRBC(N-SRBC)处理单倍型相同的亲代骨髓,以富集骨髓干细胞并去除成熟T细胞。9例缺乏组织相容性供体的重症联合免疫缺陷病(SCID)患者接受了这些SBA阴性、SRBC阴性、N-SRBC阴性的骨髓移植(0.5 - 5.0×10⁸个细胞/千克)。根据HLA分型和/或染色体分析,9例患者中有7例(78%)有T淋巴细胞植入的记录。6例患者基于免疫球蛋白水平升高、同种血凝素和/或非T细胞的HLA-DR分型显示有B细胞免疫的证据。3例患者在移植前接受了骨髓清除性化疗以治疗母胎GVHD;中性粒细胞在移植后9至17天植入,红细胞在移植后3至4周植入,血小板在移植后第17天至第49天恢复。移植后未预防性给予免疫抑制。3例患者无GVHD,2例有短暂皮疹和/或发热,2例发生轻度局限性(I期)慢性皮肤GVHD。在植入的7例患者中,5例(71%)在移植后18至35个月存活且临床状况良好,无GVHD。这些数据表明,经SBA和SRBC/N-SRBC处理的单倍型相同骨髓移植可使SCID患者实现功能性淋巴细胞植入,且无明显GVHD,可用于一些原本无生存希望的患者。