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ABO血型不合的异基因骨髓移植后因多种红细胞同种抗体导致的严重溶血性贫血。

Severe hemolytic anemia due to multiple red cell alloantibodies after an ABO-incompatible allogeneic bone marrow transplant.

作者信息

López A, de la Rubia J, Arriaga F, Jiménez C, Sanz G F, Carpio N, Marty M L

机构信息

Department of Hematology, La Fe University Hospital, Valencia, Spain.

出版信息

Transfusion. 1998 Mar;38(3):247-51. doi: 10.1046/j.1537-2995.1998.38398222868.x.

Abstract

BACKGROUND

A patient who received an ABO-incompatible allogeneic bone marrow transplant experienced three episodes of immune hemolytic anemia due to multiple red cell (RBC) alloantibodies.

CASE REPORT

A 41-year-old man with chronic myeloid leukemia received an ABO-incompatible bone marrow graft from his HLA-identical brother. Selective removal of RBCs from donor marrow before transfusion was performed by centrifugation using a continuous-flow blood cell separator. The patient was given group O Rh-positive RBCs and group A Rh-positive platelets. Prophylaxis for graft-versus-host disease consisted of cyclosporine and methotrexate. The patient experienced three hemolytic episodes, on Days 21, 35, and 160 which were due to different RBC alloantibodies (anti-K, anti-Jk(b), anti-M, IgG anti-A) produced by host lymphocytes surviving the conditioning regimen.

RESULTS

The patient was group O, Jk(b-), and the marrow donor was group A, Jk(b+). After the first hemolytic episode (Day 21), immunohematologic studies showed group O RBCs and a positive direct antiglobulin test (IgG+, C3d+). Antibody screening test and eluate studies detected anti-M, anti-Jk(b), and anti-K. During the second hemolytic episode (Day 35), the patient's blood group showed a mixed population of group A and group O RBCs. The direct antiglobulin test was positive (IgG+, C3d+). Anti-M, anti-Jk(b), and IgG anti-A were detected in the serum. Eluates made from the recipient's RBCs showed the same specificity as serum antibodies. During the third hemolytic episode (Day 160), a mixture of group O and group A RBCs was still present, the direct antiglobulin test was positive (IgG+, C3d-), and anti-Jk(b) and IgG anti-A were observed in the serum and in an eluate made from the patient's RBCs.

CONCLUSION

This is the first reported case of severe immune hemolytic anemia due to multiple RBC alloantibodies after an allogeneic bone marrow transplant. The time of appearance and the specificity of the antibodies strongly suggest that they were produced by residual recipient lymphoid cells.

摘要

背景

一名接受ABO血型不相合异基因骨髓移植的患者因多种红细胞同种抗体经历了三次免疫性溶血性贫血发作。

病例报告

一名41岁慢性髓性白血病男性患者接受了来自其HLA配型相同的兄弟的ABO血型不相合骨髓移植。在输血前,使用连续流动血细胞分离器通过离心法从供体骨髓中选择性去除红细胞。患者输注了O型Rh阳性红细胞和A型Rh阳性血小板。移植物抗宿主病的预防措施包括环孢素和甲氨蝶呤。患者在第21天、35天和160天经历了三次溶血发作,这是由于在预处理方案后存活的宿主淋巴细胞产生了不同的红细胞同种抗体(抗-K、抗-Jk(b)、抗-M、IgG抗-A)。

结果

患者血型为O型、Jk(b-),骨髓供体血型为A型、Jk(b+)。第一次溶血发作(第21天)后,免疫血液学研究显示为O型红细胞,直接抗球蛋白试验阳性(IgG+、C3d+)。抗体筛查试验和洗脱液研究检测到抗-M、抗-Jk(b)和抗-K。在第二次溶血发作(第35天)期间,患者的血型显示为A型和O型红细胞的混合群体。直接抗球蛋白试验阳性(IgG+、C3d+)。血清中检测到抗-M、抗-Jk(b)和IgG抗-A。从受者红细胞制备的洗脱液显示出与血清抗体相同的特异性。在第三次溶血发作(第160天)期间,仍存在O型和A型红细胞的混合物,直接抗球蛋白试验阳性(IgG+、C3d-),血清和从患者红细胞制备的洗脱液中观察到抗-Jk(b)和IgG抗-A。

结论

这是首例报道的异基因骨髓移植后因多种红细胞同种抗体导致严重免疫性溶血性贫血的病例。抗体出现的时间和特异性强烈表明它们是由残留的受者淋巴细胞产生的。

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