Molecular analysis and transfusion management in a rare case of cis-AB blood group: A report from India.

Transfus Clin Biol

CSIR Institute of Genomics and Integrative Biology, New Delhi, India; Academy of Scientific and Innovative Research (AcSIR), CSIR-HRDC Campus, Ghaziabad, Uttar Pradesh, India; Vishwanath Cancer Care Foundation, B 702, Neelkanth Business Park Kirol Village, Mumbai, 400 086, India. Electronic address:

Published: February 2024

AI Article Synopsis

  • The study presents a rare cis-AB blood group case in an Indian patient, marking the first molecular characterization in the Indian subcontinent.
  • Blood grouping was performed using different techniques, revealing the AB phenotype and unique agglutination reactions that aided in identification.
  • Whole exome sequencing identified two significant nucleotide changes in the ABO gene, contributing to the cis-AB phenotype, which had not been previously documented.

Article Abstract

Molecular characterization of a rare cis-AB blood group has not been done in the Indian subcontinent. Herein, we report a case of AB blood group in an Indian patient which was subsequently confirmed to be a case of cis-AB phenotype. Blood grouping was performed by the column agglutination technique (CAT), conventional tube technique (CTT) and subsequently, whole exome sequencing for molecular analysis. The patient was initially typed as AB, RhD positive in forward grouping. However, serum grouping showed agglutination (2+) with the B red cells in CAT. In CTT, an extra reaction was observed with A red cells and a strong agglutination was seen with Anti-H lectin. Thus, the blood group was identified serologically as AB. During the next-generation sequencing, a total of 10 exonic variants in the ABO gene were filtered, of which 2 (rs8176747 and rs7853989) were found to be non-synonymous and occurring on the same allele. The other allele was found to be ABO*A1.01. The sample analyzed in the study was found to carry two previously reported nucleotide changes of cis-AB (c.803G > C and c.526C > G) on the same allele which had not been reported before. Transfusion requirement was managed with type O red cells and type AB plasma.

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Source
http://dx.doi.org/10.1016/j.tracli.2023.10.001DOI Listing

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