Title of article :
Effects of TNF-α and IL-10-819 T>C single nucleotide polymorphisms on urogenital schistosomiasis in preschool children in Zimbabwe
Author/Authors :
Mduluza, Takafira Department of Infection Prevention and Control - School of Laboratory Medicine and Medical Sciences - College of Health Sciences - University of KwaZulu-Natal - Durban, South Africa , Marume, Amos Department of Infection Prevention and Control - School of Laboratory Medicine and Medical Sciences - College of Health Sciences - University of KwaZulu-Natal - Durban, South Africa , Mann, Jaclyn Department of Infection Prevention and Control - School of Laboratory Medicine and Medical Sciences - College of Health Sciences - University of KwaZulu-Natal - Durban, South Africa , Chimponda, Theresa Department of Biochemistry - Faculty of Science - University of Zimbabwe - Harare, Zimbabwe , Vengesai, Arthur Department of Biochemistry - Faculty of Science - University of Zimbabwe - Harare, Zimbabwe , Mushayi, Caroline Department of Biochemistry - Faculty of Science - University of Zimbabwe - Harare, Zimbabwe
Pages :
7
From page :
1
To page :
7
Abstract :
This study determined cytokine levels and single nucleotide polymorphisms of tumour necrosis factor (TNF)-α (rs1800629) and interleukin (IL)-10 (rs1800871) and their possible impact on susceptibility to schistosomiasis in preschool-age children in the Madziva area of Shamva district, Mashonaland Central province, Zimbabwe. Methods Urogenital schistosomiasis was diagnosed using the urine filtration method, while a sandwich enzyme-linked immunosorbent assay was used for cytokine level determination. The survey was done in August 2015 and reinfection levels post treatment were assessed at 3, 6 and 12 months. Amplification refractory mutation system polymerase chain reaction with visualisation on 2% agarose gel electrophoresis was used for genotyping. Results Schistosomiasis prevalence was found to be 10.5% (59/563). Reinfections were detected in only six children at 3 months and only one was reinfected at 12 months. There were no significant differences in TNF-α-308 G/A allele or genotype frequencies between the Schistosoma haematobium infected participants (p = 0.360) and uninfected participants (p = 0.279). However, no children with the IL-10-819 TT genotype had schistosomiasis. The TNF-α GG genotype corresponded with significantly lower TNF-α levels when compared with the GA or AA genotypes (p < 0.001), and TNF-α levels were significantly lower in infected children compared to uninfected children (p < 0.001). Conclusion Higher TNF-α levels and lower IL-10 levels are potentially protective against schistosomiasis infection. The IL-10-819 TT genotype is potentially protective against infection through its association with lower IL-10 levels.
Keywords :
protective immunity , Schistosoma haematobium , polymorphisms , cytokines susceptibility
Journal title :
African Journal of Laboratory Medicine
Serial Year :
2021
Full Text URL :
Record number :
2622744
Link To Document :
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