High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

被引:11
作者
Floch, Aline [1 ,2 ,3 ,5 ]
Gien, Dominique [3 ,4 ]
Tournamille, Christophe [1 ,2 ,3 ]
Chami, Btissam [1 ]
Habibi, Anoosha [2 ,6 ]
Galacteros, Frederic [2 ,6 ]
Bierling, Philippe [1 ,2 ,3 ,5 ,7 ]
Djoudi, Rachid [1 ]
Pondarre, Corinne [2 ,7 ]
Peyrard, Thierry [3 ,4 ]
Pirenne, France [1 ,2 ,3 ,5 ]
机构
[1] Etab Francais Sang EFS Ile France, Creteil, France
[2] INSERM, U955, Equipe Transfus & Malad Globule Rouge 2, Creteil, France
[3] Lab Excellence GR Ex, Creteil, France
[4] INTS, Dept Ctr Natl Reference Grp Sanguins, Paris, France
[5] UPEC, IMRB, Fac Med, Creteil, France
[6] Hop Univ Henri Mondor, Ctr Reference Drepanocytose, Unite Malad Globule Rouge, Creteil, France
[7] Ctr Intercommunal Creteil, Serv Pediat & Drepanocytose, Creteil, France
关键词
HEMOLYTIC TRANSFUSION REACTION; RH ANTIGEN; ALLOIMMUNIZATION; PHENOTYPE; ALLOANTIBODIES; PREVALENCE; RELEVANCE; CHILDREN; ANTIBODY; DONORS;
D O I
10.1111/trf.14633
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUNDSickle cell disease (SCD) patients undergo multiple red blood cell (RBC) transfusions and are regularly exposed to low-prevalence (LP) antigens specific to individuals of African descent. This study evaluated the prevalence of antibodies against LP antigens in SCD patients and the need to identify these antibodies in everyday practice. STUDY DESIGN AND METHODSPlasma from 211 SCD patients was tested with RBCs expressing the following LP antigens: RH10 (V), RH20 (VS), RH23 (D-W), RH30 (Go(a)), KEL6 (Js(a)), and MNS6 (He). RESULTSNine LP antibodies were found in eight patients (3.8%): five anti-RH23, two anti-RH30, and two anti-MNS6. The exposure risk, calculated for each LP antigen, was below 3% per RBC unit, for all antigens tested. Thus, in this cohort of transfused SCD patients, the prevalence of LP antibodies was similar to that of antibodies against antigens of the FY, JK, and MNS blood group systems. These findings also reveal the occurrence of anti-RH23 in SCD patients. No anti-RH20 or anti-KEL6 were found, despite the high frequency of mismatch situations. CONCLUSIONThese results highlight the immunogenicity of these LP antigens, and the evanescence of antibodies against LP antigens. They also highlight the importance of appropriate pretransfusion testing for patients frequently transfused, who are likely to be exposed to multiple types of blood group antigens.
引用
收藏
页码:1527 / 1535
页数:9
相关论文
共 42 条
  • [1] Anderson RR, 1997, AM J CLIN PATHOL, V108, P658
  • [2] Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions
    Aygun, B
    Padmanabhan, S
    Paley, C
    Chandrasekaran, V
    [J]. TRANSFUSION, 2002, 42 (01) : 37 - 43
  • [3] Predicting the effect of transfusing only phenotype-matched RBCs to patients with sickle cell disease: theoretical and practical implications
    Castro, O
    Sandler, SG
    Houston-Yu, P
    Rana, S
    [J]. TRANSFUSION, 2002, 42 (06) : 684 - 690
  • [4] Evolution of sickle cell disease from a life-threatening disease of children to a chronic disease of adults: The last 40 years
    Chaturvedi, Shruti
    DeBaun, Michael R.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2016, 91 (01) : 5 - 14
  • [5] High prevalence of red blood cell alloimmunization in sickle cell disease despite transfusion from Rh-matched minority donors
    Chou, Stella T.
    Jackson, Tannoa
    Vege, Sunitha
    Smith-Whitley, Kim
    Friedman, David F.
    Westhoff, Connie M.
    [J]. BLOOD, 2013, 122 (06) : 1062 - 1071
  • [6] NEW RH ANTIGEN AND ANTIBODY
    CHOWN, B
    LEWIS, M
    KAITA, H
    [J]. TRANSFUSION, 1962, 2 (03) : 150 - &
  • [7] RH ANTIGEN DW (WIEL)
    CHOWN, B
    KAITA, H
    PHILIPPS, S
    LEWIS, M
    [J]. TRANSFUSION, 1964, 4 (03) : 169 - &
  • [8] HEMOLYTIC DISEASE OF NEWBORN DUE TO ANTI-JS']JS
    DONOVAN, LM
    TRIPP, KL
    ZUCKERMAN, JE
    KONUGRES, AA
    [J]. TRANSFUSION, 1973, 13 (03) : 153 - 153
  • [9] Red blood cell alloimmunization is influenced by recipient inflammatory state at time of transfusion in patients with sickle cell disease
    Fasano, Ross M.
    Booth, Garrett S.
    Miles, Megan
    Du, Liping
    Koyama, Tatsuki
    Meier, Emily Riehm
    Luban, Naomi L. C.
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2015, 168 (02) : 291 - 300
  • [10] DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule
    Flegel, Willy A.
    Von Zabern, Inge
    Doescher, Andrea
    Wagner, Franz F.
    Vytiskoa, Jindra
    Pisacka, Martin
    [J]. TRANSFUSION, 2008, 48 (01) : 25 - 33