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Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method
A polymorphism in the receptor for the Fc region of IgG, Fc γ-receptor IIIa (FcγRIIIa, FCGR3A rs396991), has been inconsistently shown in the literature to have an effect on response to monoclonal antibody therapy in several indications. The rs396991 (T/G) polymorphism leads to an F176V substitution...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596484/ https://www.ncbi.nlm.nih.gov/pubmed/26367501 http://dx.doi.org/10.1097/FPC.0000000000000175 |
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author | Murphy, Kay E. Niederer, Heather A. King, Karen S. Harris, Elizabeth C. Glass, Sarah M. Cox, Charles J. |
author_facet | Murphy, Kay E. Niederer, Heather A. King, Karen S. Harris, Elizabeth C. Glass, Sarah M. Cox, Charles J. |
author_sort | Murphy, Kay E. |
collection | PubMed |
description | A polymorphism in the receptor for the Fc region of IgG, Fc γ-receptor IIIa (FcγRIIIa, FCGR3A rs396991), has been inconsistently shown in the literature to have an effect on response to monoclonal antibody therapy in several indications. The rs396991 (T/G) polymorphism leads to an F176V substitution and increased affinity for IgG. This variant has proven difficult to genotype accurately, primarily because of extensive homology between the FCGR3A and FCGR3B genes. We have shown that rs396991 can be genotyped by PCR amplification, followed by direct Sanger sequencing of the product, without coamplification of FCGR3B, and that the rs396991 TaqMan assay (C__25815666_10) agrees with Sanger sequencing results in 100% of European and Asian samples tested, but it has a small error rate in African and American populations. C__25815666_10 is therefore suitable to interrogate rs396991 in studies involving Europeans and Asians; however for other populations, the default genotyping method should be PCR followed by Sanger sequencing. |
format | Online Article Text |
id | pubmed-4596484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-45964842015-10-20 Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method Murphy, Kay E. Niederer, Heather A. King, Karen S. Harris, Elizabeth C. Glass, Sarah M. Cox, Charles J. Pharmacogenet Genomics Short Communication A polymorphism in the receptor for the Fc region of IgG, Fc γ-receptor IIIa (FcγRIIIa, FCGR3A rs396991), has been inconsistently shown in the literature to have an effect on response to monoclonal antibody therapy in several indications. The rs396991 (T/G) polymorphism leads to an F176V substitution and increased affinity for IgG. This variant has proven difficult to genotype accurately, primarily because of extensive homology between the FCGR3A and FCGR3B genes. We have shown that rs396991 can be genotyped by PCR amplification, followed by direct Sanger sequencing of the product, without coamplification of FCGR3B, and that the rs396991 TaqMan assay (C__25815666_10) agrees with Sanger sequencing results in 100% of European and Asian samples tested, but it has a small error rate in African and American populations. C__25815666_10 is therefore suitable to interrogate rs396991 in studies involving Europeans and Asians; however for other populations, the default genotyping method should be PCR followed by Sanger sequencing. Lippincott Williams & Wilkins 2015-11 2015-10-06 /pmc/articles/PMC4596484/ /pubmed/26367501 http://dx.doi.org/10.1097/FPC.0000000000000175 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0/. |
spellingShingle | Short Communication Murphy, Kay E. Niederer, Heather A. King, Karen S. Harris, Elizabeth C. Glass, Sarah M. Cox, Charles J. Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method |
title | Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method |
title_full | Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method |
title_fullStr | Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method |
title_full_unstemmed | Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method |
title_short | Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method |
title_sort | accurate interrogation of fcgr3a rs396991 in european and asian populations using a widely available taqman genotyping method |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596484/ https://www.ncbi.nlm.nih.gov/pubmed/26367501 http://dx.doi.org/10.1097/FPC.0000000000000175 |
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