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 50 条
  • [41] Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome
    Darghouth, Dhouha
    Koehl, Berengere
    Madalinski, Geoffrey
    Heilier, Jean-Francois
    Bovee, Petra
    Xu, Ying
    Olivier, Marie-Francoise
    Bartolucci, Pablo
    Benkerrou, Malika
    Pissard, Serge
    Colin, Yves
    Galacteros, Frederic
    Bosman, Giel
    Junot, Christophe
    Romeo, Paul-Henri
    BLOOD, 2011, 117 (06) : E57 - E66
  • [42] Heterogeneous Red Blood Cell Adhesion and Deformability in Sickle Cell Disease
    Yunus Alapan
    Jane A. Little
    Umut A. Gurkan
    Scientific Reports, 4
  • [43] Red blood cell alloimmunization in sickle cell disease: prevalence in 2010
    Miller, Scott T.
    Kim, Hae-Young
    Weiner, Debra L.
    Wager, Carrie G.
    Gallagher, Dianne
    Styles, Lori A.
    Dampier, Carlton D.
    Roseff, Susan D.
    TRANSFUSION, 2013, 53 (04) : 704 - 709
  • [44] Red blood cell exchange in children and adolescents with sickle cell disease
    Merlin, E.
    Hequet, O.
    Kanold, J.
    TRANSFUSION AND APHERESIS SCIENCE, 2019, 58 (02) : 136 - 141
  • [45] ECONOMIC BURDEN OF CHRONIC RED BLOOD CELL TRANSFUSIONS AMONG PATIENTS WITH SICKLE CELL DISEASE
    Kalpatthi, R.
    Song, X.
    Martinez, D.
    Black, D.
    Varker, H.
    Chan, C.
    Cong, Z.
    VALUE IN HEALTH, 2020, 23 : S335 - S335
  • [46] Red blood cell alloimmunization: lessons from sickle cell disease
    Treml, Angela
    King, Karen E.
    TRANSFUSION, 2013, 53 (04) : 692 - 695
  • [47] Red blood cell rheology and vascular dysfunction in sickle cell disease
    Connes, Philippe
    Nader, Elie
    Moeckesch, Berenike
    Charlot, Keyne
    Renoux, Celine
    Jonville, Sophie-Antoine
    Joly, Philippe
    Hardy-Dessources, Marie-Dominique
    Pialoux, Vincent
    Lemonne, Nathalie
    Romana, Marc
    ACTA PHYSIOLOGICA, 2019, 227
  • [48] Obstetric Outcomes in Sickle Cell Disease Patients Receiving Chronic Red Blood Cell Exchange
    Chang, B.
    Bai, Y.
    TRANSFUSION, 2013, 53 : 113A - 113A
  • [49] Red Blood Cell Utilization Among Patients with Sickle Cell Disease: A Single Center Experience
    Uminski, Kelsey
    Perelman, Iris
    Mack, Johnathan
    Tinmouth, Alan
    BLOOD, 2022, 140 : 10769 - 10770
  • [50] Changing practice: red blood cell typing by molecular methods for patients with sickle cell disease
    Casas, Jessica
    Friedman, David F.
    Jackson, Tannoa
    Vege, Sunitha
    Westhoff, Connie M.
    Chou, Stella T.
    TRANSFUSION, 2015, 55 (06) : 1388 - 1393