4.5 Article

Class I and II human leukocyte antibodies in pediatric haploidentical allograft candidates: prevalence and risk factors

期刊

BONE MARROW TRANSPLANTATION
卷 54, 期 8, 页码 1287-1294

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/s41409-018-0427-7

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资金

  1. National key research and development plan of China [2017YFA0104500]
  2. Foundation for Innovative Research Groups of the National Natural Science Foundation of China [81621001]
  3. National Natural Science Foundation of China [81870140, 81670166, 81873445, 81530046]
  4. Beijing Municipal Science & Technology Project [Z171100001017098, Z18111000960000]
  5. project of health collaborative innovation of Guangzhou city [201704020214]
  6. Scientific Research Foundation for Capital Medicine Development [2018-2-4084, 2016-1-4082]

向作者/读者索取更多资源

Donor-specific anti-human leukocyte antigen (HLA) antibodies (DSAs) were associated with graft failure (GF) following haploidentical stem cell transplantation (Haplo-HSCT). The prevalence and risk factors of DSAs in pediatric candidates remain to be determined. In a prospective trial (ChiCTR-OPC-15006672), 486 children with hematological diseases were enrolled to screen for the presence of anti-HLA class I and II antibodies of immunoglobulin G type. Fifty two patients (10.7%) demonstrated positive panel-reactive antibody (PRA) for class I; 24 (4.9%), for class II; and 13 (2.7%), for both. Multivariate analysis showed diagnosis was the independent risk factor for antibodies, as acute lymphoblastic leukemia (ALL) patients (HR0.141, 95% CI: 0.037-0.538, p = 0.004) had a lower incidence of class II PRAs and DSAs against HLA-B, DQ, and DR, whereas myelodysplastic syndrome (MDS) patients had a higher incidence of PRAs for both class I and class II (HR4.790, 95% CI: 1.010-22.716, p = 0.049), and DSAs against HLA-A, B, C, DP, and DQ. Older age (>12 vs. = 12) was associated with DSAs against HLA-DP (HR0.194, 95% CI: 0.041-0.918, p = 0.039). Our findings provided novel evidence for prevalence and risk factors for PRAs and DSAs in pediatric candidates receiving haplo-HSCT, possibly benefiting anti-HLA antibody monitoring and donor selection.

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