Antibodies to HBV surface antigen in relation to interferon-λ3 in hemodialysis patients

被引:9
|
作者
Grzegorzewska, Alicja E. [1 ]
Swiderska, Monika K. [2 ,3 ]
Mostowska, Adrianna [4 ]
Warchol, Wojciech [5 ]
Jagodzinski, Pawel P. [4 ]
机构
[1] Poznan Univ Med Sci, Chair & Dept Nephrol Transplantol & Internal Dis, Przybyszewskiego 49,49 Przybyszewskiego Blv, PL-60355 Poznan, Poland
[2] Poznan Univ Med Sci, Student Nephrol Res Grp, Przybyszewskiego 49, PL-60355 Poznan, Poland
[3] Poznan Univ Med Sci, Chair & Dept Nephrol Transplantol & Internal Dis, Przybyszewskiego 49, PL-60355 Poznan, Poland
[4] Poznan Univ Med Sci, Chair & Dept Biochem & Mol Biol, Swiecickiego 6, PL-60781 Poznan, Poland
[5] Poznan Univ Med Sci, Chair & Dept Biophys, Grunwaldzka 6, PL-60780 Poznan, Poland
关键词
Anti-HBs; Hemodialysis; IFNL3; Infection; Interferon-X3; Vaccination; HEPATITIS-B-VIRUS; SINGLE NUCLEOTIDE POLYMORPHISMS; GENOME-WIDE ASSOCIATION; GENE POLYMORPHISMS; INTERLEUKIN; 28B; RIBAVIRIN THERAPY; IL28B RS12979860; BINDING-PROTEIN; VACCINATION; IMMUNIZATION;
D O I
10.1016/j.vaccine.2016.08.073
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim: To investigate circulating IFN-73 and IFNL3 polymorphisms in hemodialysis (HD) patients differing in HBV surface antigen antibody (anti-HBs) production. Methods: The study included 106 HBV-vaccinated HD patients (88 developed anti-HBs) and 36 HBV-infected HD subjects (27 developed anti-HBs). Plasma IFN-lambda 3 (enzyme-linked immunosorbent assay) and rs12979860 (C > T) and rs8099917 (T > G) in IFNL3 (high-resolution melting curve analysis) were analyzed with regard to the association with anti-HBs production in response to HBV vaccination or infection. The results were adjusted for gender, age, cause of renal disease, dialysis vintage, dialysis modality, IFN-lambda 3, and 25(OH)D as appropriate. Results: HBV vaccine responders had higher circulating IFN-lambda 3 (ng/L) than non-responders (120, 36-233 vs. 53, 33-109, P < 0.000001). Patients who generated anti-HBs after HBV infection also had higher circulating IFN-lambda 3 levels than those who did not (133, 35-215 vs. 71, 9-229, P = 0.043). The IFN-lambda 3 concentration correlated with the anti-HBs titer in vaccinated (r = 0.614, P < 0.000001) and infected patients (r = 0.589, P = 0.0002). Plasma IFN-lambda 3 was the only significant indicator of responsiveness to HBV vaccination (adjusted P = 0.018) and remained the only significant associate for the development of post infection anti-HBs (adjusted P = 0.049). A plasma IFN-lambda 3 level of 85.5 ng/L was the cut-off value for the prognosis of an anti-HBs titer below vs. equal to or over 101U/L in the entire group of HD patients (ROC sensitivity 68.7%, specificity 85.2%, and AUC 0.827). Significant associations were not found between IFN-lambda 3 and IFNL3 rs12979860. Subjects treated with low flux HD that harbored the TT genotype in rs8099917 showed higher IFN-lambda 3 levels than patients bearing the G allele in rs8099917 (139, 68-233 vs. 103, 9-208, P = 0.049). Conclusion: In HD patients, circulating IFN-lambda 3 strongly correlates with anti-HBs production after HBV vaccination and infection. IFNL3 rs8099917 polymorphisms seem to be associated with IFN-lambda 3 plasma levels in HD subjects. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4866 / 4874
页数:9
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