A new blood group antigen is defined by anti-CD59, detected in a CD59-deficient patient

被引:18
作者
Anliker, Markus [1 ,2 ]
von Zabern, Inge [1 ,2 ]
Hoechsmann, Britta [1 ,2 ]
Kyrieleis, Henriette [3 ]
Dohna-Schwake, Christian [4 ]
Flegel, Willy A. [1 ,2 ,5 ]
Schrezenmeier, Hubert [1 ,2 ]
Weinstock, Christof [1 ,2 ]
机构
[1] Univ Ulm, German Red Cross Blood Transfus Serv Baden Wurtte, Inst Clin Transfus Med & Immunogenet Ulm, D-89069 Ulm, Germany
[2] Univ Ulm, Inst Transfus Med, D-89069 Ulm, Germany
[3] Hosp Bethanien, Dept Pediat, Moers, Germany
[4] Univ Hosp Essen, Dept Pediat, Essen, Germany
[5] NIH, Dept Transfus Med, Ctr Clin, Bethesda, MD 20892 USA
关键词
PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; MEMBRANE-ATTACK COMPLEX; CD59; DEFICIENCY; PROTEIN;
D O I
10.1111/trf.12531
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: CD59 is a cell surface glycoprotein of approximately 20 kDa limiting the lytic activity of the terminal complement complex C5b-9. Although CD59 is known as a red blood cell (RBC) antigen defined by monoclonal antibodies, it so far has not been identified as a blood group antigen, since the description of a human alloantibody was missing. In this study we show the presence of an anti-CD59 in a patient affected by a homozygous CD59 deficiency. STUDY DESIGN AND METHODS: RBC CD59 and CD55 were determined by flow cytometry or by the column agglutination technique using monoclonal antisera. Commercially available His-tagged recombinant soluble CD59 protein was used to inhibit anti-CD59. RESULTS: Seven cases of an isolated CD59 deficiency due to three distinct null alleles of the CD59 gene have been published so far. Recently we described the CD59-null allele c.146delA in a young child of heterozygous parents. Her plasma contained an alloantibody directed against the high-prevalence RBC antigen CD59. The antibody specificity was identified using soluble recombinant human CD59 protein, which blocked the reactivity of the patient's antibody and of monoclonal anti-CD59 but not of monoclonal anti-CD55. In addition, RBC alloantibodies such as anti-K, anti-C, anti-c, or anti-Fy(a) remained unaffected. Therefore, inhibition by recombinant CD59 is a useful diagnostic tool to detect alloantibodies in the presence of anti-CD59. CONCLUSION: This is the first demonstration of a human anti-CD59 alloantibody, which defines CD59 as an RBC blood group antigen. CD59 represents a candidate for a new blood group system.
引用
收藏
页码:1817 / 1822
页数:6
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