Donor-Specific Anti-Human Leukocyte Antigen Antibodies Predict Prolonged Isolated Thrombocytopenia and Inferior Outcomes of Haploidentical Hematopoietic Stem Cell Transplantation.
Xiaosu ZhaoXiangyu ZhaoMingrui HuoQiaozhen FanXuying PeiYu WangXiaohui ZhangLanping XuXiao-Jun HuangKaiyan LiuYing-Jun ChangPublished in: Journal of immunology research (2017)
Prolonged isolated thrombocytopenia (PT) after allogeneic stem cell transplantation (allo-SCT) has a great impact on transplant outcome. In this study, we performed a retrospective analysis to investigate the association of donor-specific anti-human leukocyte antigen (HLA) antibodies (DSAs) with PT in 394 patients who underwent unmanipulated haploidentical blood and marrow transplantation (HBMT). For HLA antibody positive samples with a median fluorescent intensity (MFI) > 500, DSAs were further examined. A total of 390 patients (99.0%) achieved sustained myeloid engraftment. Of the 394 cases tested, 45 (11.4%) were DSA positive. The cumulative incidence of PT in this cohort of patients was 9.9 ± 1.5%. The incidence of PT was higher in patients with a MFI ≥ 1000 compared with those with a MFI < 1000 (16.8 ± 6.4% versus 7.4 ± 1.4%, P = 0.05). Multivariate analysis showed that the presence of DSAs (MFI ≥ 1000) was correlated to PT (hazard ratio (HR) 3.262; 95% confidence interval (CI), 1.339-7.946; P = 0.009) and transplant-related mortality (HR 2.320; 95% CI, 1.169-4.426; P = 0.044). Our results, for the first time, suggest an association of DSAs with PT after unmanipulated HBMT. It would help screen out the suitable donor and guide intervention. This indicated that DSAs should be incorporated in the algorithm for unmanipulated HBMT.
Keyphrases
- stem cell transplantation
- end stage renal disease
- chronic kidney disease
- newly diagnosed
- ejection fraction
- randomized controlled trial
- high dose
- risk factors
- peripheral blood
- machine learning
- type diabetes
- acute myeloid leukemia
- stem cells
- immune response
- high throughput
- quantum dots
- cardiovascular disease
- mesenchymal stem cells
- high intensity
- cell therapy
- single molecule
- patient reported
- hematopoietic stem cell