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INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system

BACKGROUND: The INDIAN blood group system comprises 4 antigens sensitive to enzymes and 2-aminoethyl isothiouronium bromide (AET). AIM: The patient's antibody was investigated for its specificity to the high-frequency antigens (HFA) of this system. MATERIAL AND METHODS: Low ionic strength solut...

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Autores principales: Joshi, Sanmukh R., Sheladiya, Ankita, Mendapara-Dobariya, Kinjal V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613417/
https://www.ncbi.nlm.nih.gov/pubmed/28970678
http://dx.doi.org/10.4103/0973-6247.214337
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author Joshi, Sanmukh R.
Sheladiya, Ankita
Mendapara-Dobariya, Kinjal V.
author_facet Joshi, Sanmukh R.
Sheladiya, Ankita
Mendapara-Dobariya, Kinjal V.
author_sort Joshi, Sanmukh R.
collection PubMed
description BACKGROUND: The INDIAN blood group system comprises 4 antigens sensitive to enzymes and 2-aminoethyl isothiouronium bromide (AET). AIM: The patient's antibody was investigated for its specificity to the high-frequency antigens (HFA) of this system. MATERIAL AND METHODS: Low ionic strength solution (LISS)-tube/LISS-indirect antiglobulin test (IAT) methods were used. The patient's red blood cells (RBCs) were tested with antisera to HFA. Her antibody was tested with RBCs lacking the HFA. Furthermore, it was tested with RBCs as untreated or treated with enzyme or AET. The genetic sequence was studied for mutation in CD44 gene that encodes INDIAN antigens. RESULTS: The patient was grouped A1B, RhD+, antibody screening test positive, direct antiglobulin test negative. A negative autocontrol test had suggested to the alloantibody being present. Antibody had agglutinated RBCs in LISS-tube at RT and by LISS-IAT at 37°C. The RBCs of the 11-cell panel, those lacking HFA and from 50 random donors, were agglutinated by her antibody indicating its specificity to the HFA, though the RBCs of Lu (a-b-)/In (Lu) type showed a weaker reaction. The patient's RBCs were agglutinated by antisera to a number of the enzyme-sensitive HFA, including those of INDIAN blood groups. The antibody showed reduced reactivity with the RBCs treated with papain, chymotrypsin, and AET but resistant to trypsin and dithiothreitol. The patient's genetic sequence revealed a novel homozygous mutation 449G>A in exon 5 of CD44. CONCLUSION: The antibody to enzyme sensitive HFA was tested for serological and molecular genetics studies and found to be directed to the novel HFA, named as INRA of the INDIAN blood group system and was assigned a numerical symbol IN: 005 by the International Society of Blood Transfusion (ISBT).
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spelling pubmed-56134172017-10-02 INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system Joshi, Sanmukh R. Sheladiya, Ankita Mendapara-Dobariya, Kinjal V. Asian J Transfus Sci Original Article BACKGROUND: The INDIAN blood group system comprises 4 antigens sensitive to enzymes and 2-aminoethyl isothiouronium bromide (AET). AIM: The patient's antibody was investigated for its specificity to the high-frequency antigens (HFA) of this system. MATERIAL AND METHODS: Low ionic strength solution (LISS)-tube/LISS-indirect antiglobulin test (IAT) methods were used. The patient's red blood cells (RBCs) were tested with antisera to HFA. Her antibody was tested with RBCs lacking the HFA. Furthermore, it was tested with RBCs as untreated or treated with enzyme or AET. The genetic sequence was studied for mutation in CD44 gene that encodes INDIAN antigens. RESULTS: The patient was grouped A1B, RhD+, antibody screening test positive, direct antiglobulin test negative. A negative autocontrol test had suggested to the alloantibody being present. Antibody had agglutinated RBCs in LISS-tube at RT and by LISS-IAT at 37°C. The RBCs of the 11-cell panel, those lacking HFA and from 50 random donors, were agglutinated by her antibody indicating its specificity to the HFA, though the RBCs of Lu (a-b-)/In (Lu) type showed a weaker reaction. The patient's RBCs were agglutinated by antisera to a number of the enzyme-sensitive HFA, including those of INDIAN blood groups. The antibody showed reduced reactivity with the RBCs treated with papain, chymotrypsin, and AET but resistant to trypsin and dithiothreitol. The patient's genetic sequence revealed a novel homozygous mutation 449G>A in exon 5 of CD44. CONCLUSION: The antibody to enzyme sensitive HFA was tested for serological and molecular genetics studies and found to be directed to the novel HFA, named as INRA of the INDIAN blood group system and was assigned a numerical symbol IN: 005 by the International Society of Blood Transfusion (ISBT). Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5613417/ /pubmed/28970678 http://dx.doi.org/10.4103/0973-6247.214337 Text en Copyright: © 2017 Asian Journal of Transfusion Science http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Joshi, Sanmukh R.
Sheladiya, Ankita
Mendapara-Dobariya, Kinjal V.
INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system
title INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system
title_full INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system
title_fullStr INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system
title_full_unstemmed INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system
title_short INRA, a new high-frequency antigen in the INDIAN (IN023) blood group system
title_sort inra, a new high-frequency antigen in the indian (in023) blood group system
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613417/
https://www.ncbi.nlm.nih.gov/pubmed/28970678
http://dx.doi.org/10.4103/0973-6247.214337
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