共 30 条
Comparison of Serum HBsAg Quantitation by Four Immunoassays, and Relationships of HBsAg Level with HBV Replication and HBV Genotypes
被引:30
作者:
Tuaillon, Edouard
[1
,2
,3
]
Mondain, Anne-Marie
[2
]
Nagot, Nicolas
[1
,3
,4
]
Ottomani, Laure
[2
]
Kania, Dramane
[1
,5
]
Nogue, Erika
[4
]
Rubbo, Pierre-Alain
[1
,3
]
Pageaux, Georges-Philippe
[6
,7
]
Van de Perre, Philippe
[1
,2
]
Ducos, Jacques
[1
,2
]
机构:
[1] Univ Montpellier I, INSERM, U1058, Montpellier, France
[2] CHRU Montpellier, Dept Bacteriol Virol, Montpellier, France
[3] CHRU Montpellier, Inst Rech Biotherapie, Montpellier, France
[4] Dept Med Informat, Montpellier, France
[5] Ctr Muraz, Virol Lab, Bobo Dioulasso, Burkina Faso
[6] CHRU Montpellier, Dept Hepatogastroenterol, Montpellier, France
[7] CHRU Montpellier, INSERM, U632, Montpellier, France
来源:
关键词:
HEPATITIS-B-VIRUS;
SURFACE-ANTIGEN SEROCLEARANCE;
HBEAG-NEGATIVE PATIENTS;
SUSTAINED RESPONSE;
PEGINTERFERON ALPHA-2A;
ADEFOVIR DIPIVOXIL;
NATURAL-HISTORY;
FOLLOW-UP;
THERAPY;
LAMIVUDINE;
D O I:
10.1371/journal.pone.0032143
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Background: The decline in hepatitis B virus surface antigen (HBsAg) may be an early predictor of the viral efficacy of Hepatitis B virus (HBV) therapy. The HBsAg levels obtained by different immunoassays now need comparing and the relationships between levels of HBsAg and HBV DNA alongside HBsAg and genotype must be evaluated. Methodology/Principal Findings: HBsAg levels were compared among 80 patients using the Abbott Architect assay, a commercial immunoassay approved for HBsAg detection and quantitation, and three other assays derived from immunoassays approved for HBsAg detection (manufactured by Diasorin, Bio-Rad and Roche). Good correlation was found between the Abbot vs. Diasorin, Bio-Rad and Roche assays with narrow 95% limits of agreement and small mean differences: -0.06 to 0.11, -0.09 log(10) IU/mL; -0.57 to 0.64, -0.04 log(10) IU/mL; -0.09 to 0.45, -0.27 log(10) IU/mL, respectively. These agreements were not affected by genotypes A or D. HBsAg was weakly correlated with HBV DNA, whatever the HBsAg assay used: Abbott, rho = 0.36 p = 0.001, Diasorin rho = 0.34, p = 0.002; Bio-Rad rho = 0.37, p<0.001; or Roche rho = 0.41, p<0.001. This relationship between levels of HBsAg and HBV DNA seemed to depend on genotypes. Whereas HBsAg (Abbott assay) tended to correlate with HBV DNA for genotype A (rho = 0.44, p = 0.02), no such correlation was significant for genotypes D (rho = 0.29, p = 0.15). Conclusion/Significance: The quantitation of HBsAg in routine clinical samples is comparable between the reference assay and the adapted assays with acceptable accuracy limits, low levels of variability and minimum discrepancy. While HBsAg quantitation is not affected by HBV genotype, the observed association between levels of HBsAg and HBV DNA seems genotype dependent.
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