Detection of in vivo hepatitis B virus surface antigen mutations—A comparison of four routine screening assays

乙型肝炎表面抗原 医学 乙型肝炎病毒 病毒学 乙型肝炎 病毒
作者
Mikael Gencay,Anja Seffner,Stephan Pabinger,Jérémie Gautier,Peter Gohl,Michael Weizenegger,Dionysios Neofytos,Richard Batrla,A Woeste,Ho-Seong Kim,Gastón Westergaard,Christine Reinsch,Eva Brill,Phạm Thị Thu Thúy,B. Hoang,Mark Sonderup,C. Wendy Spearman,Giuseppina Brancaccio,M. Fasano,G.B. Gaeta,Teresa Santantonio,Wolfgang E. Kaminski
出处
期刊:Journal of Viral Hepatitis [Wiley]
卷期号:25 (10): 1132-1138 被引量:13
标识
DOI:10.1111/jvh.12915
摘要

An important requirement for a state-of-the-art hepatitis B surface antigen (HBsAg) screening assay is reliable detection of mutated HBsAg. Currently, there is a striking shortage of data regarding the detection rates of in vivo HBsAg mutations for these clinically important assays. Therefore, we compared the detection rates of four commercial HBsAg screening assays using a global cohort of 1553 patients from four continents with known HBV genotypes. These samples, which represent the broadest spectrum of known and novel HBsAg major hydrophilic region (MHR) mutations to date, were analyzed for the presence of HBsAg using the Roche Elecsys® HBsAg II Qualitative, Siemens ADVIA Centaur XP HBsAg II, Abbott Architect HBsAg Qualitative II and DiaSorin Liaison® HBsAg Qualitative assays, respectively. Of the 1553 samples, 1391 samples could be sequenced; of these, 1013 (72.8%) carried at least one of the 345 currently known amino acid substitutions (distinct HBsAg mutation) in the HBsAg MHR. All 1553 patient samples were positive for HBsAg using the Elecsys® HBsAg II Qual assay, with a sensitivity (95% confidence interval) of 99.94% (99.64%-100%), followed by the Abbott Architect 99.81% (99.44%-99.96%), Siemens ADVIA 99.81% (99.44%-99.96%) and DiaSorin Liaison® 99.36% (98.82%-99.69%) assays, respectively. Our results indicate that the Elecsys® HBsAg II Qual assay exhibits the highest sensitivity among the commercial HBsAg screening assays, and demonstrate that its capacity to detect HBV infection is not compromised by HBsAg MHR mutants.

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