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A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups

BACKGROUND: Discrepancy in “forward/reverse” grouping leads to confusion in assigning ABO group to a person. It could be genetic in nature and classified according to the presence/absent of antigen on red blood cell (RBC) vis-a-vis corresponding alloantibody in plasma. AIM: The aim of the study was...

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Autores principales: Joshi, Sanmukh R., Kanani, Ashish N., Senjaliya, Snehal B., Rajapara, Manisha M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294441/
https://www.ncbi.nlm.nih.gov/pubmed/34349451
http://dx.doi.org/10.4103/ajts.AJTS_64_19
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author Joshi, Sanmukh R.
Kanani, Ashish N.
Senjaliya, Snehal B.
Rajapara, Manisha M.
author_facet Joshi, Sanmukh R.
Kanani, Ashish N.
Senjaliya, Snehal B.
Rajapara, Manisha M.
author_sort Joshi, Sanmukh R.
collection PubMed
description BACKGROUND: Discrepancy in “forward/reverse” grouping leads to confusion in assigning ABO group to a person. It could be genetic in nature and classified according to the presence/absent of antigen on red blood cell (RBC) vis-a-vis corresponding alloantibody in plasma. AIM: The aim of the study was to investigate the grouping anomaly found in a recently delivered woman who required transfusion. MATERIALS AND METHODS: A standard protocol for investigation was followed. RESULTS: A 27-year-old female, gravida 4, para 3, was grouped O on forward grouping, but her serum did not agglutinate Group B RBCs tested. Absorption-elution study gave an active eluate from her sensitized RBCs with anti-B or anti-A+B. Saliva showed H, but no B antigens indicating to her Bel phenotype. However, 2-week latter in the follow-up study, her serum revealed a presence of complement binding high titer anti-B. The problem of missing anti-B on the previous occasion was attributed to hemagglutination inhibition caused by accumulated complement macromolecules on RBCs that gave rise to physical hindrance in the formation hemagglutination clumps. CONCLUSION: The unusual case of erroneous reversed grouping was attributed to complement-mediated hemagglutination inhibition. The positive eluate obtained from sensitized RBCs of the mother was considered to be due to a contamination of fetal RBCs in maternal circulation entered during her postpartum phase of pregnancy. It could also be due to a conversion of H to B antigen no matter in trace amount by the fetal B group-specific transferase percolated into maternal circulation.
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spelling pubmed-82944412021-08-03 A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups Joshi, Sanmukh R. Kanani, Ashish N. Senjaliya, Snehal B. Rajapara, Manisha M. Asian J Transfus Sci Original Article BACKGROUND: Discrepancy in “forward/reverse” grouping leads to confusion in assigning ABO group to a person. It could be genetic in nature and classified according to the presence/absent of antigen on red blood cell (RBC) vis-a-vis corresponding alloantibody in plasma. AIM: The aim of the study was to investigate the grouping anomaly found in a recently delivered woman who required transfusion. MATERIALS AND METHODS: A standard protocol for investigation was followed. RESULTS: A 27-year-old female, gravida 4, para 3, was grouped O on forward grouping, but her serum did not agglutinate Group B RBCs tested. Absorption-elution study gave an active eluate from her sensitized RBCs with anti-B or anti-A+B. Saliva showed H, but no B antigens indicating to her Bel phenotype. However, 2-week latter in the follow-up study, her serum revealed a presence of complement binding high titer anti-B. The problem of missing anti-B on the previous occasion was attributed to hemagglutination inhibition caused by accumulated complement macromolecules on RBCs that gave rise to physical hindrance in the formation hemagglutination clumps. CONCLUSION: The unusual case of erroneous reversed grouping was attributed to complement-mediated hemagglutination inhibition. The positive eluate obtained from sensitized RBCs of the mother was considered to be due to a contamination of fetal RBCs in maternal circulation entered during her postpartum phase of pregnancy. It could also be due to a conversion of H to B antigen no matter in trace amount by the fetal B group-specific transferase percolated into maternal circulation. Wolters Kluwer - Medknow 2021 2021-06-12 /pmc/articles/PMC8294441/ /pubmed/34349451 http://dx.doi.org/10.4103/ajts.AJTS_64_19 Text en Copyright: © 2021 Asian Journal of Transfusion Science https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Joshi, Sanmukh R.
Kanani, Ashish N.
Senjaliya, Snehal B.
Rajapara, Manisha M.
A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups
title A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups
title_full A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups
title_fullStr A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups
title_full_unstemmed A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups
title_short A novel observation on grouping anomaly: The phenomena mimicking the B(el) genetic variant of the ABO blood groups
title_sort novel observation on grouping anomaly: the phenomena mimicking the b(el) genetic variant of the abo blood groups
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294441/
https://www.ncbi.nlm.nih.gov/pubmed/34349451
http://dx.doi.org/10.4103/ajts.AJTS_64_19
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