Interleukin 17F Gene Polymorphism as a Potential Protective Factor in the Immunopathology of Ocular Toxoplasmosis

Author:

da Silva Danilo Donizete1ORCID,Frederico Fábio Batista2ORCID,Previato Mariana1,Siqueira Rubens Camargo1ORCID,Bonini‐Domingos Claudia Regina3ORCID,de Souza Victor Hugo4ORCID,Castiglioni Lilian5ORCID,Brandão Cinara Cássia1ORCID,de Mattos Luiz Carlos1ORCID,Ayo Christiane Maria1ORCID

Affiliation:

1. Laboratory of Immunogenetics, Department of Molecular Biology Faculty of Medicine of São José do Rio Preto (FAMERP) São José do Rio Preto Brazil

2. Hospital de Base of the Regional Medical Faculty Foundation (HB‐FUNFARME), Ophthalmology Outpatient Clinic São José do Rio Preto Brazil

3. Department of Biology São Paulo State University “Júlio de Mesquita Filho” (UNESP) São José do Rio Preto Brazil

4. Laboratory of Immunogenetics, Department of Basic Health Sciences State University of Maringá Maringá Brazil

5. Department of Epidemiology and Collective Health Faculty of Medicine of São José do Rio Preto (FAMERP) São José do Rio Preto Brazil

Abstract

ABSTRACTOcular toxoplasmosis (OT) is characterised by intraocular inflammation due to Toxoplasma gondii infection. Studies have found that interleukin 17 (IL‐17) plays a central role in the pathology of OT. However, nucleotide variability in IL17 and interleukin 17 receptor (IL17R) genes has not been characterised in OT. As cytokine gene polymorphisms may influence the expression of these molecules, the aim of this study was to verify whether IL17A (rs2275913), IL17F (rs763780), IL17RA (rs4819554) and IL17RC (rs708567) polymorphisms are associated with OT in a Brazilian population. This study enrolled 214 patients seropositive for T. gondii (110 with OT and 104 without) and 107 controls. Polymorphisms were identified by PCR‐restriction fragment length polymorphism analysis, validated by DNA sequencing with chi‐square and multivariate analyses being used to assess possible associations between polymorphisms and OT. Logistic regression under the dominant model revealed a protection factor against OT of the C mutant allele of the IL17F (rs763780) polymorphism. The T/C‐C/C genotypes were significantly more common in patients without OT compared to those with OT (p value = 0.0066) and controls (p value = 0.014). Findings from this study suggest that the IL17F polymorphism may have an influence in the immunopathology of OT in Brazilian individuals.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Fundação de Amparo à Pesquisa do Estado de São Paulo

Publisher

Wiley

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