A Korean family with RHD*DNT only detectable after anti-D alloimmunization

Author:

Shin Dong Woo1ORCID,Lee Gun-Hyuk2ORCID,Kim Hanah2ORCID,So Kyeong A3ORCID,Hong Yun Ji14ORCID,Hur Mina2ORCID,Park Kyoung Un14ORCID

Affiliation:

1. Department of Laboratory Medicine, Seoul National University Bundang Hospital , Seongnam , Korea

2. Department of Laboratory Medicine, Konkuk University School of Medicine , Seoul , Korea

3. Department of Obstetrics and Gynecology, Konkuk University School of Medicine , Seoul , Korea

4. Department of Laboratory Medicine, Seoul National University College of Medicine , Seoul , Korea

Abstract

Abstract Objectives Identification of DNT, a rare partial D, can be challenging, as it is difficult to distinguish from D+. This study aimed to identify DNT individuals by analyzing the DNT proband’s family members, characterize DNT, and propose management strategies. Methods Family members of the first Korean DNT proband were recruited. RHD genotyping was conducted, and weak D tests were carried out using several anti-D reagents. Results Three DNT individuals were identified among 6 family members, including 1 with an anti-D alloantibody. As DNT red cells exhibited strong reactivity with all anti-D clones, DNT was serologically indistinguishable from D+. Moreover, unusual serologic findings in DNT individuals only became apparent after anti-D alloimmunization. Conclusions We recommend DNT individuals as candidates for Rh immune globulin prophylaxis during the perinatal period and transfusions with D– blood components. An anticipatory RHD genotyping is suggested for partial D family members to prevent potential partial D individuals from becoming alloimmunized.

Funder

Operation of the Korean Rare Blood Program

Publisher

Oxford University Press (OUP)

Subject

General Medicine

Reference14 articles.

1. Blood group systems;Smart,2020

2. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype;Sandler,2017

3. It’s time to phase out “serologic weak D phenotype” and resolve D types with RHD genotyping including weak D type 4;Flegel,2020

4. It’s time to phase in RHD genotyping for patients with a serologic weak D phenotype;Sandler,2015

5. RHD*DNT (RHD*38) showing D-positive reactivity on rhesus D typing and forming anti-D antibody;Lee,2023

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