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Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method. | LitMetric

Accurate interrogation of FCGR3A rs396991 in European and Asian populations using a widely available TaqMan genotyping method.

Pharmacogenet Genomics

aGenetics bBiopharm Discovery, GlaxoSmithKline, Stevenage, UK cGenetics, GlaxoSmithKline, Research Triangle Park, North Carolina, USA.

Published: November 2015

AI Article Synopsis

  • - A specific genetic variation (polymorphism) in the FCGR3A gene, known as rs396991, may influence how patients respond to monoclonal antibody treatments, but research on this has been inconsistent.
  • - This polymorphism causes a change in the receptor that increases its affinity for IgG, but accurately determining this variant has been challenging due to similarities between the FCGR3A and FCGR3B genes.
  • - A new method involving PCR amplification and Sanger sequencing has shown reliable results for genotyping rs396991 in European and Asian samples, although a TaqMan assay has shown some inaccuracies in African and American populations.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596484PMC
http://dx.doi.org/10.1097/FPC.0000000000000175DOI Listing

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