The impact of pre-existing HLA and red blood cell antibodies on transfusion support and engraftment in sickle cell disease after nonmyeloablative hematopoietic stem cell transplantation from HLA-matched sibling donors: A prospective, single-center, observational study

被引:14
作者
Nickel, Robert Sheppard [1 ,2 ]
Flegel, Willy A. [3 ]
Adams, Sharon D. [3 ]
Hendrickson, Jeanne E. [4 ,5 ]
Liang, Hua [6 ]
Tisdale, John F. [7 ]
Hsieh, Matthew M. [7 ]
机构
[1] Childrens Natl Hosp, Div Hematol, 111 Michigan Ave NW, Washington, DC 20010 USA
[2] George Washington Univ, Sch Med & Hlth Sci, Washington, DC 20052 USA
[3] NIH, Dept Transfus Med, Clin Ctr, Bethesda, MD 20892 USA
[4] Yale Sch Med, Dept Lab Med, New Haven, CT USA
[5] Yale Sch Med, Dept Pediat, New Haven, CT USA
[6] George Washington Univ, Dept Stat, Washington, DC 20052 USA
[7] NIH, Cellular & Mol Therapeut Branch, Bldg 10, Bethesda, MD 20892 USA
关键词
Alloimmunization; HLA antibody; Bone marrow transplant; Transfusion; Sickle cell disease; Chimerism; BONE-MARROW-TRANSPLANTATION; REDUCED-INTENSITY; GRAFT FAILURE; ALLOIMMUNIZATION; CHIMERISM; ALLOANTIBODIES; CHILDREN; ASSOCIATION; RISK;
D O I
10.1016/j.eclinm.2020.100432
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Hematopoietic stem cell transplantation (HSCT) is curative for patients with sickle cell disease (SCD). Prior to HSCT, patients with SCD commonly receive RBC transfusions with some becoming RBC or HLA alloimmunized. This alloimmunization may impact post-HSCT transfusion requirements and donor engraftment. Methods: The study population included patients with SCD transplanted on a single-center nonmyeloablative, HLA-matched sibling HSCT trial at the National Heart, Lung, and Blood Institute (NHLBI) who had a pre-HSCT sample available for HLA class I antibody testing. We evaluated transfusion requirements and engraftment outcomes comparing patients with and without pre-existing HLA and RBC antibodies. Findings: Of 36 patients studied, 10 (28%) had HLA class I antibodies and 11 (31%) had a history of RBC alloantibodies. Up to day +45 post-HSCT, patients with HLA antibodies received more platelet transfusions (median 2.5 vs 1, p = 0.042) and those with RBC alloantibodies received more RBC units (median 7 vs 4, p = 0.0059) compared to respective non-alloimmunized patients. HLA alloimmunization was not associated with neutrophil engraftment, donor chimerism, or graft rejection. However, RBC alloimmunization correlated with a decreased donor T cell chimerism at 1 year (median 24% vs 55%, p = 0.035). Interpretation: Pre-existing HLA and RBC alloantibodies are clinically significant for patients undergoing HLA-matched nonmyeloablative HSCT. Testing for both HLA and RBC antibodies is important to help estimate transfusion needs peri-HSCT. The association of lower donor T cell chimerism and pre-existing RBC alloantibodies needs further investigation. (C) 2020 The Authors. Published by Elsevier Ltd.
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页数:7
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