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2019, Number 3

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Rev Biomed 2019; 30 (3)

Role of single nucleotide polymorphisnm of interleukin 12 and IFNgamma expression in antibody response to recombinant hepatitis B vaccine

Montalvo-Villalba MC, Barroso-González P, Lopez-Hernández D, Bello-Corredor M, Marrero-Sánchez B, Rodriguez-Lay LA
Full text How to cite this article

Language: Spanish
References: 16
Page: 143--151
PDF size: 280.50 Kb.


Key words:

anti-HBsAg, single nucleotide polymorphism, Interleukin 12, health care workers.

ABSTRACT

Introduction. Host genetic factors like polymorphism of cytokine genes and the integrity of axis interleukin 12/interferon gamma (IL-12/INF-γ) could be related with anti-HBsAg response induced after HBV vaccination.
Objectives. To determinate the influence of single nucleotide polymorphism (SNP) of IL-12 and INF-γ mRNA expression in the antibody response to recombinant vaccine against hepatitis B virus.
Material and Methods. Twelve health care workers without protective titers of anti-HBsAg were boosted with one dose of Heberbiovac HB. In addition, it was included four controls with anti-HBsAg titres ›100IU/l. SNP of IL-12A e IL-12B were identified by nucleotide sequencing. UMELISA kit was used to quantify anti-HBsAg levels at 7 and 28 days post-vaccination (DPV). IFNg mRNA expression was determined by RT-PCR real time in mononuclear cells stimulated with HBsAg obtained from vaccine.
Results. High anti-HBsAg levels (›1000IU/l) were detected in 75% (9/12) workers at 28 DPV, high frequency it was observed in the IL-12A/IL-12B allelic genotypic combinations GG/AC and GG/AA (77,7%, 7/9). Low anti- HBsAg protective levels (11-79UI/l) at 28 DPV and IFN-γ mRNA expression were detected in individuals who carried AA/AA y GG/AA (25%, 3/12) combinations. Individual with AA/AA genotype had a negative anti-HBsAg seroconversion from 33 to 11UI/l at 7 and 28 DPV.
Conclusions. SNP of IL-12 and IFN-γ expression could be mediating the quality of anti-HBsAg titers after one booster dose of Heberbiovac HB. Further studies are needed in order to identify the relevance of these and others molecular markers in immune response against HBV vaccine.


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Rev Biomed. 2019;30