RhD alloimmunization by DEL variant missed in donor testing.


Journal

Transfusion
ISSN: 1537-2995
Titre abrégé: Transfusion
Pays: United States
ID NLM: 0417360

Informations de publication

Date de publication:
05 2022
Historique:
revised: 13 02 2022
received: 26 01 2022
accepted: 01 03 2022
pubmed: 24 3 2022
medline: 11 5 2022
entrez: 23 3 2022
Statut: ppublish

Résumé

Exposure to normal or variably expressed RhD antigens in an antigen-negative individual can elicit an immune response and lead to the formation of clinically significant anti-D alloantibodies. We present the case of anti-D alloimmunization by DEL variant missed in routine blood donor screening. Blood donors were typed for D antigen using the direct serologic micromethod. Nonreactive samples were confirmed in the indirect antiglobulin method with an IgM/IgG anti-D monoclonal reagent. Genomic DNA was extracted using a commercial QIAamp DNA Blood Mini kit on the QIAcube device (Qiaqen, Germany). RHD genotyping was performed using the PCR-SSP genotyping kits- Ready Gene D weak, Ready Gene D weak screen, Ready Gene CDE, and Ready Gene D AddOn (Inno-Train, Germany). Unidentified alleles were sent for DNA genome sequencing. After identifying DEL positive blood units in RhD negative blood donor pool, a look-back study was performed to determine if their previous donations caused alloimmunization in recipients. Out of 40 D negative recipients, one developed anti-D alloantibody after 45 days. The patient did not receive other RhD positive blood products. Blood donor typed D negative in direct and indirect agglutination method. RHD screening was positive, but RHD genotyping and DNA sequencing showed no mutation indicating the normal genotype. Currently used methods in RHD genotyping are insufficient to identify many variant alleles, especially intronic variations. We suggest additional gene investigation including yet unexplored regions of regulation and intron regions to justify our serological finding.

Identifiants

pubmed: 35318689
doi: 10.1111/trf.16862
doi:

Substances chimiques

Blood Group Antigens 0
Isoantibodies 0
Rh-Hr Blood-Group System 0
DNA 9007-49-2

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1084-1088

Informations de copyright

© 2022 AABB.

Références

Daniels G. Variants of RhD - current testing and clinical consequences. Br J Haemato. 2013;161:461-70.
Harmening DM. Modern blood banking & transfusion practices. 7th ed. Philadelphia, USA: F.A. Davis Company; 2019.
Scott SA, Nagl L, Tilley L, Liew YW, Condon J, Flower R, et al. The RHD(1227G>A) DEL-associated allele is the most prevalent DEL allele in Australian D- blood donors with C+ and/or E+ phenotypes. Transfusion. 2014;54(11):2931-40.
Sandler SG, Chen LN, Flegel WA. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype. Br J Haematol. 2017;179(1):10-9.
Wagner FF. Getting comfortable with RH blood group system terminologies and databases. ISBT Sci Ser. 2019;14:24-31.
Flegel WA. Molecular genetics and clinical applications for RH. Transfus Apher Sci. 2011;44(1):81-91.
http://www.rhesusbase.info/. Accessed on 2nd September, 2021.
Kwon DH, Sandler SG, Flegel WA. DEL phenotype. Immunohematology. 2017;33(3):125-32. 18:159-62.
Yin Q, Flegel WA. DEL in China: the D antigen among serologic RhD-negative individuals. J Transl Med. 2021;19(1):439.
Wagner FF. RHD PCR of D negative blood donors. Transf Med Hemother. 2013;40:172-81.
Flegel WA, Wagner FF. DEL. Blood Transfus. 2020;18(3):159-62.
Flegel WA. Homing in on D antigen immunogenicity. Transfusion. 2005;45:466-8.
Tormey CA, Hendrickson JE. Transfusion-related red blood cell allonaitbodies:induction and consequences. Blood. 2019;133:1821-30.
Safic Stanic H, Dogic V, Herceg I, Jagnjic S, Bingulac-Popovic J, Babic I, et al. D variants in the population of D-negative blood donors in the north-eastern region of Croatia. Transfus Med. 2021;31:43-7.
Stack G, Tormey CA. Detection rate of blood group alloimmunization based on real-world testing practices and kincetics of antibody induction and evanescence. Transfusion. 2016;56:2662-7.
Gunson HH, Stratton F, Cooper DG, Rawlinson VI. Primary immunization of Rh-negative volunteers. Br Med J. 1970;1(5696):593-5.
Flegel WA, Wagner FF, Ó Donghaile DP. Anti-D immunization rates may exceed 50% in many clinically relevant settings, despite varying widely among patient cohorts. Transfusion. 2020;60(5):1109-10.
Dunbar NM, Yazar MH. OPTIMUS study investigators on behalf of the biomedical excellence for safer transfusion (BEST) collaborative. O- product transfusion, invventory managment and utilization during shortage: the Optimus study. Transfusion. 2018;58:1348-55.
Selleng K, Jenichen G, Denker K. Emergency transfusion of patients with unknown blood type with blood group O Rhesus D positive red blood cells concentarete: a prospective, single-center observational study. Lancet Hematol. 2017;4:e218-24.
Tchakarov A, Hobbs R, Bai Y. Transfusion of D+ red blood cells to D- individuals in trauma situations. Immunohematology. 2014;30(4):149-52.
Raval JS, Madden KM, Neal MD, Moore SA. Anti-D alloimmunization in Rh(D) negative adults with severe traumatic injury. Transfusion. 2021;61:S144-9.
Arora K, Kelley J, Sui D, Ning J, Martinez F, Lichtiger B, et al. Cancer type predicts alloimmunization following RhD-incompatible RBC transfusions. Transfusion. 2017;57(4):952-8.
Sandler SG, Flegel WA. Does tranfusion of Asian-type DEL red blood cells to D-recipients cause D alloimmunization. Transfusion. 2019;59:2455-7.
Wagner T, Körmöczi GF, Buchta C, Vadon M, Lanzer G, Mayr WR, et al. Anti-D immunization by DEL red blood cells. Transfusion. 2005;45(4):520-6.
Wagner FF, Frohmajer A, Flegel WA. RHD positive haplotypes in D negative Europeans. BMC Genet. 2001;2:10.
St-Louis M, Lebrun A, Goldman M, Lavoie M. Alloimmunization of patients by blood units harboring distinct DEL variants. Immunohematology. 2013;29(4):136-40.
Krog GR, Clausen FB, Berkowicz A, Jørgensen L, Rieneck K, Nielsen LK, et al. Is current serologie RhD typing of blood donors sufficient for avoiding immunization of recipients? Transfusion. 2011;51:2278-85.
Dias R, Finney RD, Humphreys D, Graham L. Rhesus Du incompatibility in a newborn with high levels of anti D and a benign clinical course. Vox Sang. 1986;50(1):52-3.
Dava NR, Upadhyaya A, Agarwal N, Mehta A, Choudhary V, Goyal G. A rare case of hemolytic disease of newborn due to weak D (D unknown) antigen in child. Asian J Transfus Sci. 2018;12(1):75-7.
Tammi SM, Tounsi WA, Sainio S, Kiernan M, Avent ND, Madgett TE, et al. Next-generation sequencing of 35 RHD variants in 16 253 serologically D- pregnant women in the Finnish population. Blood Adv. 2020;4(20):4994-5001.

Auteurs

Hana Safic Stanic (H)

Department of Immunohematology, Croatian Institute of Transfusion Medicine, Zagreb, Croatia.

Vesna Dogic (V)

Department of Molecular Diagnostics, Croatian Institute of Transfusion Medicine, Zagreb, Croatia.

Jasna Bingulac-Popovic (J)

Department of Molecular Diagnostics, Croatian Institute of Transfusion Medicine, Zagreb, Croatia.

Zrinka Kruhonja Galic (Z)

Department of Immunohematology, Croatian Institute of Transfusion Medicine, Zagreb, Croatia.

Miljana Stojic Vidovic (M)

Department for Blood donor testing, Croatian Institute of Transfusion Medicine, Zagreb, Croatia.

Kresimir Puljic (K)

Department for woman's psychotic disorders, University Psychiatric Hospital "Vrapče", Zagreb, Croatia.

Irena Jukic (I)

Medical Department, Croatian Institute of Transfusion Medicine, Zagreb, Croatia.
Faculty of Medicine, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH