Exploring IL-17 gene promoter polymorphisms in canine leishmaniasis

被引:2
|
作者
Goncalves-de-Albuquerque, Suenia da C. [1 ,2 ]
da Silva, Lidiane Gomes [3 ]
De Sousa-Paula, Lucas Christian [1 ]
da Silva Sales, Kamila Gaudencio [1 ]
Boegel, Annette [4 ]
Dantas-Torres, Filipe [1 ]
机构
[1] Oswald Cruz Fdn Fiocruz, Aggeu Magalhaes Inst, Dept Immunol, Recife, PE, Brazil
[2] Cent Lab Publ Hlth Dr Milton Bezerra Sobral, Recife, PE, Brazil
[3] Univ Ctr Vale Ipojuca, Caruaru, PE, Brazil
[4] Elanco, Monheim, Germany
关键词
Interleukin; 17; Canine leishmaniasis; Immunogenetics; Single nucleotide polymorphisms; Immunopathogenesis; PROTECTION; INFANTUM; ASTHMA; CELLS;
D O I
10.1016/j.actatropica.2022.106452
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Proinflammatory cytokine secretion determines the infection course in leishmaniasis. The immunopathology of canine leishmaniasis (CanL) caused by Leishmania infantum is characterized by low Leishmania-specific IFN-gamma and IL-17 production. Mutations in the human IL-17 gene promoter alter cytokine expression and may increase the susceptibility of humans to some infectious diseases. In this study, we correlated canine IL-17 single nucleotide polymorphisms (SNPs) with anti-Leishmania IgG levels, parasite load and external clinical signs in dogs naturally exposed to L. infantum in Brazil. A higher frequency (Chi-square test: X-2= 5.378, df= 1, P= 0.020) of major alleles was observed among dogs showing no external clinical signs attributable to Leishmania infection. A high proportion of A allele carriers (mutant) were observed among dogs with high antibody levels, although differences were not statistically significant (Chi-square test: X-2= 4.410, df= 4, P= 0.353), as compared to dogs with low antibody levels. In general, the association of canine IL-17 SNPs with disease expression or disease exasperation did not reach enough statistical power to allow the use of these mutations as prognostic markers. This knowledge may pave the way for further investigations on the genetic aspects of CanL and its immunotherapy.
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页数:7
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