TY - JOUR
T1 - Association of DRB1*11 and DRB1*12 alleles of the HLA system with the evolution of the Hepatitis B virus infection in Burkina Faso
AU - Zongo, Sidnooma Véronique
AU - Djigma, Florencia Wendkuuni
AU - Yonli, Albert Théophane
AU - Sorgho, Pegdwendé Abel
AU - Nagalo, Bolni Marius
AU - Traore, Lassina
AU - Somda, Dogfounianalo
AU - Amegnona, Lanyo Jospin
AU - Languie, Eugène
AU - Some, Couna Christiane Bere
AU - Sia, Lydie Marie Jeannette
AU - Sourabie, Issa Boaffi
AU - Sombie, Roger Arsène
AU - Serme, Abdel Karim
AU - Obiri-Yeboah, Dorcas
AU - Simpore, Jacques
N1 - Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Nature B.V.
PY - 2023
Y1 - 2023
N2 - Background: Hepatitis B Virus (HBV) infection affect all social strata of humanity and in the absence of any management, this infection has a different outcome from one infected person to another. This suggests that there are specific individual factors that influence the outcome of the pathology. Sex, immunogenetics and age of contraction of the virus have been cited as factors that influence the evolution of the pathology. In this study, we looked at two alleles of the Human Leucocyte Antigen (HLA) system to measure their possible involvement in the evolution of HBV infection. Method and results: We conducted a cohort study involving 144 individuals spread over 04 distinct stages of infection and then compared allelic frequencies in these populations. A multiplex PCR was conducted and the data obtained was analyzed using R and SPSS software. Our study revealed a predominance of HLA-DRB1*12 in our study population without, however, showing a significant difference between HLA-DRB1*11 and HLA-DRB1*12. The HLA-DRB1*12 proportion was significantly higher in chronic hepatitis B (CHB) and resolved hepatitis B (RHB) compared to cirrhosis and hepatocellular carcinoma (HCC) (p-value = 0,002). Carrying HLA-DRB1*12 has been associated with a low risk of complication of infection (CHB → cirrhosis; OR 0,33 p-value 0,017; RHB → HCC OR 0,13; p-value = 0,00,045) whereas the presence of HLA-DRB1*11 in the absence of HLA-DRB1*12 increased the risk of developing severe liver disease. However, a strong interaction of these alleles with the environment could modulate the infection. Conclusion: Our study shown that HLA-DRB1*12 is the most frequent and it’s carriage may be protective in the development of infection.
AB - Background: Hepatitis B Virus (HBV) infection affect all social strata of humanity and in the absence of any management, this infection has a different outcome from one infected person to another. This suggests that there are specific individual factors that influence the outcome of the pathology. Sex, immunogenetics and age of contraction of the virus have been cited as factors that influence the evolution of the pathology. In this study, we looked at two alleles of the Human Leucocyte Antigen (HLA) system to measure their possible involvement in the evolution of HBV infection. Method and results: We conducted a cohort study involving 144 individuals spread over 04 distinct stages of infection and then compared allelic frequencies in these populations. A multiplex PCR was conducted and the data obtained was analyzed using R and SPSS software. Our study revealed a predominance of HLA-DRB1*12 in our study population without, however, showing a significant difference between HLA-DRB1*11 and HLA-DRB1*12. The HLA-DRB1*12 proportion was significantly higher in chronic hepatitis B (CHB) and resolved hepatitis B (RHB) compared to cirrhosis and hepatocellular carcinoma (HCC) (p-value = 0,002). Carrying HLA-DRB1*12 has been associated with a low risk of complication of infection (CHB → cirrhosis; OR 0,33 p-value 0,017; RHB → HCC OR 0,13; p-value = 0,00,045) whereas the presence of HLA-DRB1*11 in the absence of HLA-DRB1*12 increased the risk of developing severe liver disease. However, a strong interaction of these alleles with the environment could modulate the infection. Conclusion: Our study shown that HLA-DRB1*12 is the most frequent and it’s carriage may be protective in the development of infection.
KW - 11
KW - 12
KW - Burkina Faso
KW - Cirrhosis
KW - DRB1
KW - DRB1
KW - HBV
KW - HCC
KW - HLA
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U2 - 10.1007/s11033-023-08353-0
DO - 10.1007/s11033-023-08353-0
M3 - Article
AN - SCOPUS:85153629127
SN - 0301-4851
JO - Molecular Biology Reports
JF - Molecular Biology Reports
ER -